Broadly neutralizing antibodies to SARS-CoV-2 and other human coronaviruses
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a recently emerged pathogenic human coronavirus that belongs to the sarbecovirus lineage of the genus Betacoronavirus. The ancestor strain has evolved into a number of variants of concern, with the Omicron variant of concern now having...
Saved in:
Published in | Nature reviews. Immunology Vol. 23; no. 3; pp. 189 - 199 |
---|---|
Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
01.03.2023
Nature Publishing Group |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a recently emerged pathogenic human coronavirus that belongs to the sarbecovirus lineage of the genus Betacoronavirus. The ancestor strain has evolved into a number of variants of concern, with the Omicron variant of concern now having many distinct sublineages. The ongoing COVID-19 pandemic caused by SARS-CoV-2 has caused serious damage to public health and the global economy, and one strategy to combat COVID-19 has been the development of broadly neutralizing antibodies for prophylactic and therapeutic use. Many are in preclinical and clinical development, and a few have been approved for emergency use. Here we summarize neutralizing antibodies that target four key regions within the SARS-CoV-2 spike (S) protein, namely the N-terminal domain and the receptor-binding domain in the S1 subunit, and the stem helix region and the fusion peptide region in the S2 subunit. Understanding the characteristics of these broadly neutralizing antibodies will accelerate the development of new antibody therapeutics and provide guidance for the rational design of next-generation vaccines.
The ancestral strain of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has evolved into a number of variants of concern. In this Review, Wang and colleagues discuss progress in the development and characterization of broadly neutralizing antibodies to SARS-CoV-2, which may lead to new antibody therapeutics and inform the design of next-generation vaccines. |
---|---|
AbstractList | Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a recently emerged pathogenic human coronavirus that belongs to the sarbecovirus lineage of the genus Betacoronavirus. The ancestor strain has evolved into a number of variants of concern, with the Omicron variant of concern now having many distinct sublineages. The ongoing COVID-19 pandemic caused by SARS-CoV-2 has caused serious damage to public health and the global economy, and one strategy to combat COVID-19 has been the development of broadly neutralizing antibodies for prophylactic and therapeutic use. Many are in preclinical and clinical development, and a few have been approved for emergency use. Here we summarize neutralizing antibodies that target four key regions within the SARS-CoV-2 spike (S) protein, namely the N-terminal domain and the receptor-binding domain in the S1 subunit, and the stem helix region and the fusion peptide region in the S2 subunit. Understanding the characteristics of these broadly neutralizing antibodies will accelerate the development of new antibody therapeutics and provide guidance for the rational design of next-generation vaccines.The ancestral strain of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has evolved into a number of variants of concern. In this Review, Wang and colleagues discuss progress in the development and characterization of broadly neutralizing antibodies to SARS-CoV-2, which may lead to new antibody therapeutics and inform the design of next-generation vaccines. Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a recently emerged pathogenic human coronavirus that belongs to the sarbecovirus lineage of the genus Betacoronavirus. The ancestor strain has evolved into a number of variants of concern, with the Omicron variant of concern now having many distinct sublineages. The ongoing COVID-19 pandemic caused by SARS-CoV-2 has caused serious damage to public health and the global economy, and one strategy to combat COVID-19 has been the development of broadly neutralizing antibodies for prophylactic and therapeutic use. Many are in preclinical and clinical development, and a few have been approved for emergency use. Here we summarize neutralizing antibodies that target four key regions within the SARS-CoV-2 spike (S) protein, namely the N-terminal domain and the receptor-binding domain in the S1 subunit, and the stem helix region and the fusion peptide region in the S2 subunit. Understanding the characteristics of these broadly neutralizing antibodies will accelerate the development of new antibody therapeutics and provide guidance for the rational design of next-generation vaccines. The ancestral strain of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has evolved into a number of variants of concern. In this Review, Wang and colleagues discuss progress in the development and characterization of broadly neutralizing antibodies to SARS-CoV-2, which may lead to new antibody therapeutics and inform the design of next-generation vaccines. Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a recently emerged pathogenic human coronavirus that belongs to the sarbecovirus lineage of the genus Betacoronavirus. The ancestor strain has evolved into a number of variants of concern, with the Omicron variant of concern now having many distinct sublineages. The ongoing COVID-19 pandemic caused by SARS-CoV-2 has caused serious damage to public health and the global economy, and one strategy to combat COVID-19 has been the development of broadly neutralizing antibodies for prophylactic and therapeutic use. Many are in preclinical and clinical development, and a few have been approved for emergency use. Here we summarize neutralizing antibodies that target four key regions within the SARS-CoV-2 spike (S) protein, namely the N-terminal domain and the receptor-binding domain in the S1 subunit, and the stem helix region and the fusion peptide region in the S2 subunit. Understanding the characteristics of these broadly neutralizing antibodies will accelerate the development of new antibody therapeutics and provide guidance for the rational design of next-generation vaccines.Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a recently emerged pathogenic human coronavirus that belongs to the sarbecovirus lineage of the genus Betacoronavirus. The ancestor strain has evolved into a number of variants of concern, with the Omicron variant of concern now having many distinct sublineages. The ongoing COVID-19 pandemic caused by SARS-CoV-2 has caused serious damage to public health and the global economy, and one strategy to combat COVID-19 has been the development of broadly neutralizing antibodies for prophylactic and therapeutic use. Many are in preclinical and clinical development, and a few have been approved for emergency use. Here we summarize neutralizing antibodies that target four key regions within the SARS-CoV-2 spike (S) protein, namely the N-terminal domain and the receptor-binding domain in the S1 subunit, and the stem helix region and the fusion peptide region in the S2 subunit. Understanding the characteristics of these broadly neutralizing antibodies will accelerate the development of new antibody therapeutics and provide guidance for the rational design of next-generation vaccines. Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a recently emerged pathogenic human coronavirus that belongs to the sarbecovirus lineage of the genus Betacoronavirus. The ancestor strain has evolved into a number of variants of concern, with the Omicron variant of concern now having many distinct sublineages. The ongoing COVID-19 pandemic caused by SARS-CoV-2 has caused serious damage to public health and the global economy, and one strategy to combat COVID-19 has been the development of broadly neutralizing antibodies for prophylactic and therapeutic use. Many are in preclinical and clinical development, and a few have been approved for emergency use. Here we summarize neutralizing antibodies that target four key regions within the SARS-CoV-2 spike (S) protein, namely the N-terminal domain and the receptor-binding domain in the S1 subunit, and the stem helix region and the fusion peptide region in the S2 subunit. Understanding the characteristics of these broadly neutralizing antibodies will accelerate the development of new antibody therapeutics and provide guidance for the rational design of next-generation vaccines. |
Author | Zhou, Hao Jiang, Shibo Chen, Yanjia Zhu, Huanzhang Zhao, Xiaoyu Wang, Pengfei |
Author_xml | – sequence: 1 givenname: Yanjia surname: Chen fullname: Chen, Yanjia organization: State Key Laboratory of Genetic Engineering, Shanghai Institute of Infectious Disease and Biosecurity, School of Life Sciences, Fudan University – sequence: 2 givenname: Xiaoyu surname: Zhao fullname: Zhao, Xiaoyu organization: State Key Laboratory of Genetic Engineering, Shanghai Institute of Infectious Disease and Biosecurity, School of Life Sciences, Fudan University – sequence: 3 givenname: Hao orcidid: 0000-0002-0092-7987 surname: Zhou fullname: Zhou, Hao organization: Department of Microbiology, Grossman School of Medicine, New York University, College of Medical Technology, Chengdu University of Traditional Chinese Medicine – sequence: 4 givenname: Huanzhang surname: Zhu fullname: Zhu, Huanzhang organization: State Key Laboratory of Genetic Engineering, Shanghai Institute of Infectious Disease and Biosecurity, School of Life Sciences, Fudan University – sequence: 5 givenname: Shibo orcidid: 0000-0001-8283-7135 surname: Jiang fullname: Jiang, Shibo email: shibojiang@fudan.edu.cn organization: Key Laboratory of Medical Molecular Virology (MOE/NHC/CAMS), Shanghai Institute of Infectious Disease and Biosecurity, School of Basic Medical Sciences, Fudan University – sequence: 6 givenname: Pengfei orcidid: 0000-0003-2454-7652 surname: Wang fullname: Wang, Pengfei email: pengfei_wang@fudan.edu.cn organization: State Key Laboratory of Genetic Engineering, Shanghai Institute of Infectious Disease and Biosecurity, School of Life Sciences, Fudan University |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/36168054$$D View this record in MEDLINE/PubMed |
BookMark | eNp9UUlr3DAUFiEhW_sHciiGXnpRqmetcymkQ5eQQCBLr0K25BkFj5RKdiD99ZU76WQ55CTB-7b3vgO0HWJwCB0BOQZC1efMgEuJSV1jQqRimG6hfWCSYZAMtjd_SvfQQc63hIAok120RwUIRTjbR2dfUzS2f6iCG4dkev_Hh0VlwuCbaL3L1RCrq5PLKzyPv3BdBraKw9KlajmuTKjamGIw9z6N2eV3aKczfXbvH99DdPP92_X8Jz6_-HE6PznHLWdkwIJQ21nKOysYaahqWdMIBqAEM6YDMyOE844K2VggUvLWGD6jDiy3VjlH6SH6sta9G5uVs60LU3J9l_zKpAcdjdcvJ8Ev9SLe6xkHBkIUgU-PAin-Hl0e9Mrn1vW9CS6OWdcS1EzUxbVAP76C3sYxhbJeQalSg5B8EvzwPNEmyv87F0C9BrQp5pxct4EA0VOZel2mLmXqf2XqyVu9IrV-MIOP01a-f5tK19RcfMLCpafYb7D-AmyDsy0 |
CitedBy_id | crossref_primary_10_1371_journal_pone_0289198 crossref_primary_10_4049_jimmunol_2300315 crossref_primary_10_1038_s41467_024_52808_2 crossref_primary_10_1128_mbio_00679_23 crossref_primary_10_1038_s41421_024_00648_1 crossref_primary_10_3390_ijms24065352 crossref_primary_10_3390_vaccines12111214 crossref_primary_10_1016_j_immuni_2024_08_017 crossref_primary_10_3390_vaccines12101089 crossref_primary_10_1186_s12864_024_09977_7 crossref_primary_10_1128_spectrum_02808_24 crossref_primary_10_3390_ani15030422 crossref_primary_10_1016_j_bsheal_2024_09_002 crossref_primary_10_1128_jvi_00416_24 crossref_primary_10_3389_fimmu_2023_1099629 crossref_primary_10_1016_j_it_2023_09_006 crossref_primary_10_1128_mbio_02477_23 crossref_primary_10_1021_acs_jproteome_3c00569 crossref_primary_10_1039_D1CS01170G crossref_primary_10_1038_s41392_023_01724_w crossref_primary_10_1080_1062936X_2024_2306336 crossref_primary_10_1038_s41467_023_39890_8 crossref_primary_10_3389_fimmu_2024_1341313 crossref_primary_10_1073_pnas_2220948120 crossref_primary_10_1177_11769343241272415 crossref_primary_10_1002_jmv_70134 crossref_primary_10_3389_fimmu_2023_1192395 crossref_primary_10_1016_j_smim_2023_101828 crossref_primary_10_3390_biom13091283 crossref_primary_10_3390_ijms25158180 crossref_primary_10_1126_sciimmunol_ade0958 crossref_primary_10_1038_s41579_024_01036_y crossref_primary_10_1016_j_celrep_2024_114265 crossref_primary_10_3389_fpls_2023_1275228 crossref_primary_10_1016_j_cell_2024_09_043 crossref_primary_10_3389_fimmu_2025_1550279 crossref_primary_10_4049_immunohorizons_2200003 crossref_primary_10_1038_s41467_025_56114_3 crossref_primary_10_1038_s41577_023_00858_w crossref_primary_10_1038_s41598_024_72491_z crossref_primary_10_1093_infdis_jiae249 crossref_primary_10_1080_22221751_2023_2244084 crossref_primary_10_3390_vaccines12030218 crossref_primary_10_2222_jsv_73_153 crossref_primary_10_1016_j_ajps_2023_100855 crossref_primary_10_1038_s41598_024_76506_7 crossref_primary_10_2217_nnm_2022_0316 crossref_primary_10_7554_eLife_95708 crossref_primary_10_1186_s12879_024_10345_9 crossref_primary_10_2174_0113816128334441241108050528 crossref_primary_10_1093_glycob_cwaf001 crossref_primary_10_3390_v15030687 crossref_primary_10_3390_vaccines12070738 crossref_primary_10_1002_jmv_29628 crossref_primary_10_3389_fimmu_2023_1252367 crossref_primary_10_1038_s43586_023_00246_7 crossref_primary_10_1021_acs_analchem_4c01165 crossref_primary_10_1038_s41392_024_01917_x crossref_primary_10_1038_s42003_024_07422_9 crossref_primary_10_1016_j_antiviral_2024_105834 crossref_primary_10_3390_vaccines13010009 crossref_primary_10_1093_infdis_jiad523 crossref_primary_10_1016_j_heliyon_2024_e34925 crossref_primary_10_1080_22221751_2024_2412990 crossref_primary_10_1172_JCI168080 crossref_primary_10_1093_bfgp_elad051 crossref_primary_10_1186_s12985_025_02667_0 crossref_primary_10_3390_v16020217 crossref_primary_10_3389_fmolb_2024_1389548 crossref_primary_10_1016_j_imlet_2024_106887 crossref_primary_10_1186_s12967_025_06162_6 crossref_primary_10_1038_s41392_023_01615_0 crossref_primary_10_3389_fimmu_2023_1307693 crossref_primary_10_1016_j_ejmech_2025_117450 crossref_primary_10_3390_v16030484 crossref_primary_10_1016_j_ebiom_2024_105354 crossref_primary_10_1016_j_virol_2024_110067 crossref_primary_10_1016_j_isci_2024_110326 crossref_primary_10_1016_j_isci_2024_110208 crossref_primary_10_1038_s41392_024_02043_4 crossref_primary_10_1021_acsnano_4c12212 crossref_primary_10_3390_vaccines11020408 crossref_primary_10_1016_j_isci_2024_110354 crossref_primary_10_1038_s41541_024_00817_z crossref_primary_10_1016_j_isci_2024_110470 crossref_primary_10_1371_journal_ppat_1012383 crossref_primary_10_3390_vaccines12040342 crossref_primary_10_1016_j_ijbiomac_2025_141417 crossref_primary_10_3389_fmolb_2023_1288686 crossref_primary_10_1016_j_cell_2023_04_024 crossref_primary_10_3389_fcimb_2024_1415885 crossref_primary_10_3390_v16030472 crossref_primary_10_1016_j_celbio_2025_100017 crossref_primary_10_1016_j_coviro_2023_101349 crossref_primary_10_1002_jmv_28440 crossref_primary_10_1038_s41467_023_42408_x crossref_primary_10_1186_s12951_025_03243_y crossref_primary_10_1016_j_nbt_2023_12_004 crossref_primary_10_3389_fcimb_2023_1239700 crossref_primary_10_1128_mbio_00741_24 crossref_primary_10_3390_vaccines11091451 crossref_primary_10_1128_spectrum_03655_23 crossref_primary_10_1016_j_antiviral_2024_105820 crossref_primary_10_1002_jmv_70071 crossref_primary_10_1080_21645515_2024_2388344 crossref_primary_10_1080_22221751_2024_2412643 crossref_primary_10_3389_fimmu_2023_1273938 crossref_primary_10_1038_s42003_025_07769_7 crossref_primary_10_1016_j_isci_2024_109363 crossref_primary_10_3390_ijms26020587 crossref_primary_10_1016_j_biopha_2025_117936 crossref_primary_10_1155_2024_8871439 crossref_primary_10_1021_acsptsci_5c00122 crossref_primary_10_1111_febs_16777 crossref_primary_10_1021_acsomega_3c07947 crossref_primary_10_1111_imr_13431 crossref_primary_10_3390_epidemiologia5020013 crossref_primary_10_1021_acscentsci_4c00722 crossref_primary_10_1128_jvi_01137_23 crossref_primary_10_1134_S000629792309002X crossref_primary_10_1128_mbio_03220_23 crossref_primary_10_1371_journal_ppat_1012599 crossref_primary_10_1016_j_vaccine_2025_126744 crossref_primary_10_1360_SSV_2023_0084 crossref_primary_10_1002_jmv_28900 crossref_primary_10_3390_vaccines11111644 crossref_primary_10_1016_j_bbrc_2025_151558 crossref_primary_10_3390_v15061253 crossref_primary_10_1016_j_biopha_2023_115292 crossref_primary_10_7759_cureus_60015 crossref_primary_10_1128_msphere_00393_24 crossref_primary_10_1128_spectrum_02892_23 crossref_primary_10_3390_microorganisms12030617 crossref_primary_10_3390_v15091901 crossref_primary_10_1371_journal_pcbi_1012215 crossref_primary_10_1038_s41586_024_08477_8 crossref_primary_10_7554_eLife_95708_3 crossref_primary_10_3390_vaccines12080914 crossref_primary_10_3390_vaccines12080919 crossref_primary_10_1016_S1473_3099_23_00454_1 crossref_primary_10_1371_journal_ppat_1011804 crossref_primary_10_3390_v15040917 crossref_primary_10_1016_j_tips_2024_10_007 crossref_primary_10_3390_vaccines12040417 crossref_primary_10_1371_journal_ppat_1012456 crossref_primary_10_1021_acs_analchem_3c04372 crossref_primary_10_1016_j_chempr_2024_10_021 crossref_primary_10_1016_j_it_2023_11_006 crossref_primary_10_1002_adhm_202402744 crossref_primary_10_1016_j_cej_2025_159386 crossref_primary_10_1021_acs_analchem_4c04913 crossref_primary_10_1080_14712598_2024_2388186 crossref_primary_10_3389_fimmu_2023_1160065 crossref_primary_10_1016_j_micinf_2024_105461 crossref_primary_10_3389_fcimb_2024_1407261 crossref_primary_10_1038_s41573_023_00672_y crossref_primary_10_3390_molecules29215206 crossref_primary_10_1016_j_jcvp_2024_100192 crossref_primary_10_3390_ijms25094642 crossref_primary_10_3390_v16020177 crossref_primary_10_1002_rmv_2464 crossref_primary_10_3390_vaccines13030255 crossref_primary_10_1016_j_ijbiomac_2023_125997 crossref_primary_10_1126_scitranslmed_adn0396 crossref_primary_10_1016_j_bbadis_2025_167772 crossref_primary_10_3390_antib13020041 crossref_primary_10_4103_ijmr_ijmr_2591_22 crossref_primary_10_1073_pnas_2414583121 crossref_primary_10_1038_s41551_025_01353_4 crossref_primary_10_1002_mco2_426 crossref_primary_10_1073_pnas_2410529121 crossref_primary_10_1080_21645515_2023_2281733 crossref_primary_10_1371_journal_pone_0298033 crossref_primary_10_1002_adfm_202315442 crossref_primary_10_7717_peerj_17846 crossref_primary_10_7841_ksbbj_2024_39_3_83 crossref_primary_10_3390_vaccines12020129 crossref_primary_10_3390_vaccines11111727 crossref_primary_10_3390_app142311048 crossref_primary_10_1073_pnas_2314518121 crossref_primary_10_1038_s41590_024_01776_2 crossref_primary_10_3390_ijms24020908 crossref_primary_10_1002_jmv_29122 crossref_primary_10_1038_s41467_024_49096_1 crossref_primary_10_1093_procel_pwae007 crossref_primary_10_1111_pbi_14458 crossref_primary_10_1128_jvi_00929_23 crossref_primary_10_3390_ijms25052585 crossref_primary_10_3389_fimmu_2024_1514226 crossref_primary_10_1016_j_biopha_2024_116900 crossref_primary_10_31631_2073_3046_2024_23_6_169_176 crossref_primary_10_31857_S0320972523090026 crossref_primary_10_1093_trstmh_trae060 crossref_primary_10_1208_s12248_025_01043_8 crossref_primary_10_3390_vaccines12090977 crossref_primary_10_1371_journal_ppat_1012650 crossref_primary_10_1128_mbio_00067_24 crossref_primary_10_1088_1742_5468_ad1be7 crossref_primary_10_1126_sciadv_ade3470 crossref_primary_10_1126_sciadv_adk6425 crossref_primary_10_3390_antib12010005 crossref_primary_10_1016_j_bsheal_2025_01_001 |
Cites_doi | 10.1080/22221751.2022.2030200 10.1126/science.abc6952 10.1126/science.abb7269 10.1038/s41579-020-00459-7 10.1016/j.celrep.2021.109771 10.1101/2022.05.13.491770 10.1016/j.cell.2022.03.009 10.1038/s41392-021-00810-1 10.1038/s41586-020-2456-9 10.1038/s41392-021-00740-y 10.1126/science.abf4830 10.1126/science.abc5881 10.1038/s41586-020-2349-y 10.1126/science.abd2321 10.1101/2022.07.18.500332 10.1128/JVI.06540-11 10.1371/journal.ppat.1005578 10.1016/j.immuni.2022.04.003 10.1038/s41577-020-00480-0 10.1126/science.abh1766 10.1080/21645515.2020.1740560 10.1002/prot.25497 10.1126/science.abe3255 10.1038/s41467-021-25331-x 10.1038/s41586-021-03398-2 10.1038/s41586-021-03817-4 10.3390/ijms21124546 10.1038/nrmicro775 10.1038/nature12005 10.1073/pnas.2205784119 10.1016/j.immuni.2020.10.023 10.1016/10.1038/s41564-022-01198-6 10.1126/science.abm8143 10.1126/scitranslmed.abj5413 10.1128/mBio.02473-21 10.1016/j.celrep.2021.109928 10.1038/s41586-020-2548-6 10.1080/22221751.2020.1742076 10.1038/s41586-020-2571-7 10.1038/s41586-021-03908-2 10.1101/2022.07.28.501852 10.1126/science.abq2679 10.1038/s41590-022-01138-w 10.1016/j.chom.2021.04.007 10.1101/2022.01.12.22269023 10.1002/wnan.1697 10.3389/fcimb.2020.587269 10.1038/s41594-020-0480-y 10.1086/655654 10.26508/lsa.202000786 10.1038/s41564-020-0695-z 10.1016/j.celrep.2022.110812 10.1016/j.chom.2021.04.010 10.1126/science.abj3321 10.1016/j.isci.2022.104914 10.1016/S1473-3099(22)00524-2 10.1016/j.str.2021.05.014 10.1126/science.abc2241 10.1126/science.abn8897 10.1038/s41586-020-2380-z 10.1038/s41586-021-03461-y 10.1101/2022.02.01.478504 10.1126/science.abq3773 10.1080/22221751.2021.2011623 10.1016/j.meegid.2020.104502 10.1186/s40249-020-00662-x 10.1038/s41586-020-2852-1 10.1038/s41590-022-01248-5 10.1038/s41401-020-0485-4 10.1038/nrmicro.2016.81 10.1128/cmr.00014-22 10.1038/s41586-020-2012-7 10.3390/v13020202 10.1038/mi.2013.23 10.1016/j.cell.2021.03.029 10.1016/j.bj.2020.11.011 10.1038/s41586-022-04980-y 10.1128/microbiolspec.AID-0012-2013 10.1056/NEJMoa2029849 10.1038/s41586-021-04386-2 10.7326/M20-6976 10.1128/JVI.01762-16 10.1016/j.str.2022.06.004 10.1038/s41586-020-2381-y 10.1038/s41589-021-00832-4 10.1126/scitranslmed.abi9215 10.1038/s41586-021-03807-6 10.1038/s41467-020-20602-5 10.1016/j.cell.2021.03.028 10.1186/s12985-015-0439-5 10.1073/pnas.0400762101 10.1016/j.bpc.2020.106420 10.1016/j.chom.2021.03.005 10.3389/fimmu.2021.752003 10.1038/s41422-022-00612-2 10.1016/j.celrep.2021.109679 10.1038/s41564-022-01155-3 10.1126/sciimmunol.add5446 10.1080/19420862.2021.1922134 10.1016/j.chom.2022.05.001 10.1016/j.isci.2021.102479 10.1126/science.abd0827 10.1016/j.jbc.2021.100306 10.1126/scitranslmed.abj7125 10.1038/s41586-022-05053-w |
ContentType | Journal Article |
Copyright | Springer Nature Limited 2022. Springer Nature or its licensor holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. 2022. Springer Nature Limited. Springer Nature Limited 2022, Springer Nature or its licensor holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. |
Copyright_xml | – notice: Springer Nature Limited 2022. Springer Nature or its licensor holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. – notice: 2022. Springer Nature Limited. – notice: Springer Nature Limited 2022, Springer Nature or its licensor holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. |
DBID | AAYXX CITATION CGR CUY CVF ECM EIF NPM 3V. 7QR 7RV 7T5 7U9 7X7 7XB 88E 8AO 8C1 8FD 8FE 8FH 8FI 8FJ 8FK ABUWG AEUYN AFKRA AZQEC BBNVY BENPR BHPHI CCPQU DWQXO FR3 FYUFA GHDGH GNUQQ H94 HCIFZ K9. KB0 LK8 M0S M1P M7N M7P NAPCQ P64 PHGZM PHGZT PJZUB PKEHL PPXIY PQEST PQGLB PQQKQ PQUKI PRINS 7X8 5PM |
DOI | 10.1038/s41577-022-00784-3 |
DatabaseName | CrossRef Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed ProQuest Central (Corporate) Chemoreception Abstracts Nursing & Allied Health Database Immunology Abstracts Virology and AIDS Abstracts Health & Medical Collection ProQuest Central (purchase pre-March 2016) Medical Database (Alumni Edition) ProQuest Pharma Collection Public Health Database Technology Research Database ProQuest SciTech Collection ProQuest Natural Science Collection Hospital Premium Collection Hospital Premium Collection (Alumni Edition) ProQuest Central (Alumni) (purchase pre-March 2016) ProQuest Central (Alumni) ProQuest One Sustainability ProQuest Central UK/Ireland ProQuest Central Essentials Biological Science Collection ProQuest Central Natural Science Collection ProQuest One ProQuest Central Korea Engineering Research Database Health Research Premium Collection Health Research Premium Collection (Alumni) ProQuest Central Student AIDS and Cancer Research Abstracts SciTech Premium Collection ProQuest Health & Medical Complete (Alumni) Nursing & Allied Health Database (Alumni Edition) ProQuest Biological Science Collection ProQuest Health & Medical Collection Medical Database Algology Mycology and Protozoology Abstracts (Microbiology C) Biological Science Database Nursing & Allied Health Premium Biotechnology and BioEngineering Abstracts ProQuest Central Premium ProQuest One Academic (New) ProQuest Health & Medical Research Collection ProQuest One Academic Middle East (New) ProQuest One Health & Nursing ProQuest One Academic Eastern Edition (DO NOT USE) ProQuest One Applied & Life Sciences ProQuest One Academic ProQuest One Academic UKI Edition ProQuest Central China MEDLINE - Academic PubMed Central (Full Participant titles) |
DatabaseTitle | CrossRef MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) ProQuest Central Student Technology Research Database ProQuest One Academic Middle East (New) ProQuest Central Essentials ProQuest Health & Medical Complete (Alumni) ProQuest Central (Alumni Edition) SciTech Premium Collection ProQuest One Community College ProQuest One Health & Nursing ProQuest Natural Science Collection ProQuest Pharma Collection ProQuest Central China ProQuest Central ProQuest One Applied & Life Sciences ProQuest One Sustainability ProQuest Health & Medical Research Collection Health Research Premium Collection Health and Medicine Complete (Alumni Edition) Natural Science Collection ProQuest Central Korea Algology Mycology and Protozoology Abstracts (Microbiology C) Health & Medical Research Collection Biological Science Collection AIDS and Cancer Research Abstracts Chemoreception Abstracts ProQuest Central (New) ProQuest Medical Library (Alumni) ProQuest Public Health Virology and AIDS Abstracts ProQuest Biological Science Collection ProQuest One Academic Eastern Edition ProQuest Nursing & Allied Health Source ProQuest Hospital Collection Health Research Premium Collection (Alumni) Biological Science Database ProQuest SciTech Collection ProQuest Hospital Collection (Alumni) Biotechnology and BioEngineering Abstracts Nursing & Allied Health Premium ProQuest Health & Medical Complete ProQuest Medical Library ProQuest One Academic UKI Edition Immunology Abstracts ProQuest Nursing & Allied Health Source (Alumni) Engineering Research Database ProQuest One Academic ProQuest One Academic (New) ProQuest Central (Alumni) MEDLINE - Academic |
DatabaseTitleList | ProQuest Central Student MEDLINE - Academic MEDLINE |
Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database – sequence: 2 dbid: EIF name: MEDLINE url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search sourceTypes: Index Database – sequence: 3 dbid: BENPR name: ProQuest Central url: https://www.proquest.com/central sourceTypes: Aggregation Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Medicine Biology Public Health |
EISSN | 1474-1741 |
EndPage | 199 |
ExternalDocumentID | PMC9514166 36168054 10_1038_s41577_022_00784_3 |
Genre | Research Support, Non-U.S. Gov't Journal Article Review |
GroupedDBID | --- .55 0R~ 123 29M 36B 39C 3V. 4.4 53G 70F 7RV 7X7 88E 8AO 8C1 8FE 8FH 8FI 8FJ 8R4 8R5 AAEEF AARCD AAWYQ AAYZH AAZLF ABAWZ ABDBF ABJNI ABLJU ABNNU ABUWG ACGFS ACIWK ACPRK ACRPL ACUHS ADBBV ADNMO AENEX AEUYN AFBBN AFKRA AFRAH AFSHS AGAYW AGGDT AGHTU AHBCP AHMBA AHOSX AHSBF AIBTJ AIYXT ALFFA ALIPV ALMA_UNASSIGNED_HOLDINGS ARMCB ASPBG AVWKF AXYYD AZFZN B0M BBNVY BENPR BHPHI BKEYQ BKKNO BPHCQ BVXVI CCPQU CS3 DB5 DU5 EAD EAP EBC EBD EBS EE. EJD EMB EMK EMOBN EPL ESX EX3 EXGXG F5P FEDTE FQGFK FSGXE FYUFA HCIFZ HMCUK HVGLF HZ~ IAO IHR IHW INH INR ISR ITC L-9 LK8 M1P M7P N9A NAPCQ NNMJJ O9- ODYON P2P PQQKQ PROAC PSQYO Q2X RNR RNT RNTTT SHXYY SIXXV SNYQT SOJ SV3 TAOOD TBHMF TDRGL TSG TUS UKHRP WOW X7M ~8M AAYXX ABFSG ACSTC AEZWR AFANA AFHIU AHWEU AIXLP ALPWD ATHPR CITATION PHGZM PHGZT CGR CUY CVF ECM EIF NFIDA NPM 7QR 7T5 7U9 7XB 8FD 8FK AZQEC DWQXO FR3 GNUQQ H94 K9. M7N P64 PJZUB PKEHL PPXIY PQEST PQGLB PQUKI PRINS PUEGO 7X8 5PM |
ID | FETCH-LOGICAL-c540t-603dfd35fd640b38c4bb6411864aaf1a90055f367bd10775caa593e1d5dd8ee33 |
IEDL.DBID | 7X7 |
ISSN | 1474-1733 1474-1741 |
IngestDate | Thu Aug 21 18:39:21 EDT 2025 Thu Jul 10 22:02:40 EDT 2025 Sat Aug 23 14:28:10 EDT 2025 Thu Apr 03 06:57:02 EDT 2025 Tue Jul 01 04:15:27 EDT 2025 Thu Apr 24 23:10:18 EDT 2025 Fri Feb 21 02:37:46 EST 2025 |
IsDoiOpenAccess | true |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 3 |
Language | English |
License | 2022. Springer Nature Limited. This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c540t-603dfd35fd640b38c4bb6411864aaf1a90055f367bd10775caa593e1d5dd8ee33 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 ObjectType-Review-3 content type line 23 |
ORCID | 0000-0002-0092-7987 0000-0001-8283-7135 0000-0003-2454-7652 |
OpenAccessLink | https://pubmed.ncbi.nlm.nih.gov/PMC9514166 |
PMID | 36168054 |
PQID | 2781036756 |
PQPubID | 27582 |
PageCount | 11 |
ParticipantIDs | pubmedcentral_primary_oai_pubmedcentral_nih_gov_9514166 proquest_miscellaneous_2718962593 proquest_journals_2781036756 pubmed_primary_36168054 crossref_primary_10_1038_s41577_022_00784_3 crossref_citationtrail_10_1038_s41577_022_00784_3 springer_journals_10_1038_s41577_022_00784_3 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2023-03-01 |
PublicationDateYYYYMMDD | 2023-03-01 |
PublicationDate_xml | – month: 03 year: 2023 text: 2023-03-01 day: 01 |
PublicationDecade | 2020 |
PublicationPlace | London |
PublicationPlace_xml | – name: London – name: England |
PublicationTitle | Nature reviews. Immunology |
PublicationTitleAbbrev | Nat Rev Immunol |
PublicationTitleAlternate | Nat Rev Immunol |
PublicationYear | 2023 |
Publisher | Nature Publishing Group UK Nature Publishing Group |
Publisher_xml | – name: Nature Publishing Group UK – name: Nature Publishing Group |
References | Li (CR19) 2020; 264 Chen (CR51) 2021; 384 Bestle (CR20) 2020; 3 Stadler (CR2) 2003; 1 Barnes (CR41) 2020; 588 Rappazzo (CR68) 2021; 371 Martinez (CR69) 2022; 14 Shi (CR85) 2022 Mitchell, Colwell (CR94) 2018; 86 Yuan (CR64) 2020; 368 Rouet (CR92) 2021; 13 Zhou (CR104) 2022 Westendorf (CR57) 2022 Li (CR100) 2022; 23 Kumar (CR76) 2022 Zhou (CR48) 2022; 376 Wang (CR32) 2021; 593 Banach (CR44) 2021; 37 Woo (CR12) 2012; 86 Wang (CR61) 2022; 608 Suryadevara (CR28) 2021; 184 Moog (CR22) 2014; 7 Dacon (CR86) 2022; 377 Wu (CR73) 2020; 368 Low (CR87) 2022; 377 Cerutti (CR30) 2021; 29 Hansen (CR53) 2020; 369 Yang (CR25) 2020; 9 Yuan (CR72) 2020; 369 Tortorici (CR66) 2021; 597 Cao (CR62) 2022 Liu, Li, Jin, Liu (CR93) 2021; 13 Cerutti (CR34) 2021; 37 Fouchier (CR13) 2004; 101 (CR5) 2020; 5 Jaworski (CR9) 2021; 44 Dai, Gao (CR105) 2021; 21 McCallum (CR33) 2021; 184 Pinto (CR83) 2021; 373 Park (CR49) 2022; 375 Hu, Guo, Zhou, Shi (CR4) 2021; 19 Liu (CR29) 2020; 584 Li, Li, Zhang, Wang (CR16) 2020; 9 Luo (CR63) 2022 Liu (CR106) 2022; 32 Chen (CR90) 2022 Starr (CR47) 2021; 597 Wang (CR58) 2021; 373 Makdasi (CR37) 2021; 36 Alter, Moody (CR26) 2010; 202 Lv (CR71) 2020; 369 Haslwanter (CR39) 2021; 12 Liu (CR70) 2020; 53 Sun (CR88) 2022; 7 Stanfield, Wilson (CR95) 2014 Shi (CR42) 2020; 584 Li (CR78) 2022; 185 Ju (CR77) 2020; 584 Zhou (CR84) 2022; 14 Chen (CR102) 2022; 6 Huang, Yang, Xu, Xu, Liu (CR15) 2020; 41 Raj (CR18) 2013; 495 Ku (CR99) 2022 Bayati, Kumar, Francis, McPherson (CR21) 2021; 296 Mackay, Arden (CR1) 2015; 12 Chi (CR27) 2020; 369 Wang (CR8) 2020; 10 Du (CR101) 2021; 12 Chen, Hotez, Bottazzi (CR52) 2020; 16 Robbiani (CR74) 2020; 584 Cho (CR98) 2021; 13 Turelli (CR60) 2022 Noy-Porat (CR38) 2021; 24 de Wit, van Doremalen, Falzarano, Munster (CR17) 2016; 14 Wang (CR35) 2022; 11 Annavajhala (CR45) 2021; 597 Shrestha, Tedla, Bull (CR82) 2021; 12 Schoof (CR96) 2020; 370 Lok (CR31) 2021; 29 Yang (CR79) 2021; 6 Wang (CR65) 2022; 11 Kim (CR43) 2021; 12 Llanes (CR14) 2020; 21 Oran, Topol (CR10) 2021; 174 Zost (CR54) 2020; 584 Sharma, Ahmad Farouk, Lal (CR11) 2021; 13 Yuan (CR67) 2022; 119 Tan (CR24) 2016; 12 Cao (CR80) 2022; 608 Ai (CR36) 2022; 30 Zhou (CR6) 2020; 579 Pinto (CR56) 2020; 583 De Gasparo (CR97) 2021; 593 Umakanthan (CR3) 2020; 96 Cameroni (CR50) 2022; 602 Fenwick (CR59) 2022 Zhao (CR89) 2022 Qi, Liu, Wang, Zhang (CR103) 2022; 23 Cheeseman (CR23) 2017; 91 Wang (CR40) 2022; 55 Zhou (CR75) 2020; 27 Sheward (CR81) 2022 Wellner (CR91) 2021; 17 Wang (CR46) 2021; 29 Cerutti (CR55) 2021; 29 Kirtipal, Bharadwaj, Kang (CR7) 2020; 85 P Wang (784_CR46) 2021; 29 Coronaviridae Study Group of the International Committee on Taxonomy of Viruses. (784_CR5) 2020; 5 SJ Zost (784_CR54) 2020; 584 H Cho (784_CR98) 2021; 13 L Liu (784_CR29) 2020; 584 A Llanes (784_CR14) 2020; 21 DR Martinez (784_CR69) 2022; 14 X Wang (784_CR35) 2022; 11 MY Li (784_CR16) 2020; 9 X Chi (784_CR27) 2020; 369 D Pinto (784_CR83) 2021; 373 Y Cao (784_CR80) 2022; 608 WH Chen (784_CR52) 2020; 16 M Schoof (784_CR96) 2020; 370 L Dai (784_CR105) 2021; 21 F Yang (784_CR25) 2020; 9 M McCallum (784_CR33) 2021; 184 E Cameroni (784_CR50) 2022; 602 MK Annavajhala (784_CR45) 2021; 597 E de Wit (784_CR17) 2016; 14 J Ai (784_CR36) 2022; 30 C Li (784_CR78) 2022; 185 S Luo (784_CR63) 2022 Z Yang (784_CR79) 2021; 6 Z Ku (784_CR99) 2022 M Yuan (784_CR67) 2022; 119 M Yuan (784_CR64) 2020; 368 S Umakanthan (784_CR3) 2020; 96 LB Shrestha (784_CR82) 2021; 12 R Rouet (784_CR92) 2021; 13 X Sun (784_CR88) 2022; 7 Z Li (784_CR100) 2022; 23 J Hansen (784_CR53) 2020; 369 D Bestle (784_CR20) 2020; 3 P Wang (784_CR32) 2021; 593 Y Cao (784_CR62) 2022 M Yuan (784_CR72) 2020; 369 H Zhou (784_CR104) 2022 M Liu (784_CR93) 2021; 13 RA Fouchier (784_CR13) 2004; 101 A Wellner (784_CR91) 2021; 17 W Li (784_CR19) 2020; 264 Z Chen (784_CR90) 2022 A Sharma (784_CR11) 2021; 13 H Liu (784_CR70) 2020; 53 HM Cheeseman (784_CR23) 2017; 91 VS Raj (784_CR18) 2013; 495 Y Chen (784_CR102) 2022; 6 DP Oran (784_CR10) 2021; 174 Y Du (784_CR101) 2021; 12 Q Wang (784_CR61) 2022; 608 CG Rappazzo (784_CR68) 2021; 371 C Moog (784_CR22) 2014; 7 BB Banach (784_CR44) 2021; 37 G Cerutti (784_CR55) 2021; 29 R De Gasparo (784_CR97) 2021; 593 K Stadler (784_CR2) 2003; 1 MY Wang (784_CR8) 2020; 10 P Zhou (784_CR6) 2020; 579 PC Woo (784_CR12) 2012; 86 SM Lok (784_CR31) 2021; 29 JS Low (784_CR87) 2022; 377 IM Mackay (784_CR1) 2015; 12 R Shi (784_CR42) 2020; 584 C Dacon (784_CR86) 2022; 377 K Westendorf (784_CR57) 2022 B Ju (784_CR77) 2020; 584 G Cerutti (784_CR34) 2021; 37 H Qi (784_CR103) 2022; 23 D Haslwanter (784_CR39) 2021; 12 P Turelli (784_CR60) 2022 G Alter (784_CR26) 2010; 202 MA Tortorici (784_CR66) 2021; 597 Z Lv (784_CR71) 2020; 369 Y Huang (784_CR15) 2020; 41 B Hu (784_CR4) 2021; 19 E Makdasi (784_CR37) 2021; 36 CO Barnes (784_CR41) 2020; 588 Y Wu (784_CR73) 2020; 368 P Chen (784_CR51) 2021; 384 P Wang (784_CR65) 2022; 11 S Kumar (784_CR76) 2022 YJ Park (784_CR49) 2022; 375 TN Starr (784_CR47) 2021; 597 DF Robbiani (784_CR74) 2020; 584 DJ Sheward (784_CR81) 2022 LS Mitchell (784_CR94) 2018; 86 C Fenwick (784_CR59) 2022 F Zhao (784_CR89) 2022 D Pinto (784_CR56) 2020; 583 A Bayati (784_CR21) 2021; 296 D Zhou (784_CR75) 2020; 27 G Cerutti (784_CR30) 2021; 29 N Kirtipal (784_CR7) 2020; 85 P Zhou (784_CR84) 2022; 14 W Shi (784_CR85) 2022 Z Wang (784_CR40) 2022; 55 T Zhou (784_CR48) 2022; 376 T Noy-Porat (784_CR38) 2021; 24 C Kim (784_CR43) 2021; 12 JP Jaworski (784_CR9) 2021; 44 Z Liu (784_CR106) 2022; 32 GS Tan (784_CR24) 2016; 12 RL Stanfield (784_CR95) 2014 N Suryadevara (784_CR28) 2021; 184 L Wang (784_CR58) 2021; 373 |
References_xml | – volume: 11 start-page: 477 year: 2022 end-page: 481 ident: CR35 article-title: Homologous or heterologous booster of inactivated vaccine reduces SARS-CoV-2 Omicron variant escape from neutralizing antibodies publication-title: Emerg. Microbes Infect. doi: 10.1080/22221751.2022.2030200 – volume: 369 start-page: 650 year: 2020 end-page: 655 ident: CR27 article-title: A neutralizing human antibody binds to the N-terminal domain of the Spike protein of SARS-CoV-2 publication-title: Science doi: 10.1126/science.abc6952 – volume: 368 start-page: 630 year: 2020 end-page: 633 ident: CR64 article-title: A highly conserved cryptic epitope in the receptor binding domains of SARS-CoV-2 and SARS-CoV publication-title: Science doi: 10.1126/science.abb7269 – volume: 19 start-page: 141 year: 2021 end-page: 154 ident: CR4 article-title: Characteristics of SARS-CoV-2 and COVID-19 publication-title: Nat. Rev. Microbiol. doi: 10.1038/s41579-020-00459-7 – volume: 37 start-page: 109771 year: 2021 ident: CR44 article-title: Paired heavy- and light-chain signatures contribute to potent SARS-CoV-2 neutralization in public antibody responses publication-title: Cell Rep. doi: 10.1016/j.celrep.2021.109771 – year: 2022 ident: CR76 article-title: Structural insights for neutralization of BA.1 and BA.2 Omicron variants by a broadly neutralizing SARS-CoV-2 antibody publication-title: bioRxiv doi: 10.1101/2022.05.13.491770 – volume: 185 start-page: 1389 year: 2022 end-page: 1401 ident: CR78 article-title: Broad neutralization of SARS-CoV-2 variants by an inhalable bispecific single-domain antibody publication-title: Cell doi: 10.1016/j.cell.2022.03.009 – volume: 6 start-page: 378 year: 2021 ident: CR79 article-title: A non-ACE2 competing human single-domain antibody confers broad neutralization against SARS-CoV-2 and circulating variants publication-title: Signal. Transduct. Target. Ther. doi: 10.1038/s41392-021-00810-1 – volume: 584 start-page: 437 year: 2020 end-page: 442 ident: CR74 article-title: Convergent antibody responses to SARS-CoV-2 in convalescent individuals publication-title: Nature doi: 10.1038/s41586-020-2456-9 – volume: 6 start-page: 315 year: 2022 ident: CR102 article-title: ACE2-targeting monoclonal antibody as potent and broad-spectrum coronavirus blocker publication-title: Signal. Transduct. Target. Ther. doi: 10.1038/s41392-021-00740-y – volume: 371 start-page: 823 year: 2021 end-page: 829 ident: CR68 article-title: Broad and potent activity against SARS-like viruses by an engineered human monoclonal antibody publication-title: Science doi: 10.1126/science.abf4830 – volume: 369 start-page: 1505 year: 2020 end-page: 1509 ident: CR71 article-title: Structural basis for neutralization of SARS-CoV-2 and SARS-CoV by a potent therapeutic antibody publication-title: Science doi: 10.1126/science.abc5881 – volume: 583 start-page: 290 year: 2020 end-page: 295 ident: CR56 article-title: Cross-neutralization of SARS-CoV-2 by a human monoclonal SARS-CoV antibody publication-title: Nature doi: 10.1038/s41586-020-2349-y – volume: 369 start-page: 1119 year: 2020 end-page: 1123 ident: CR72 article-title: Structural basis of a shared antibody response to SARS-CoV-2 publication-title: Science doi: 10.1126/science.abd2321 – year: 2022 ident: CR62 article-title: Characterizations of enhanced infectivity and antibody evasion of Omicron BA.2.75 publication-title: bioRxiv doi: 10.1101/2022.07.18.500332 – volume: 86 start-page: 3995 year: 2012 end-page: 4008 ident: CR12 article-title: Discovery of seven novel mammalian and avian coronaviruses in the genus deltacoronavirus supports bat coronaviruses as the gene source of alphacoronavirus and betacoronavirus and avian coronaviruses as the gene source of gammacoronavirus and deltacoronavirus publication-title: J. Virol. doi: 10.1128/JVI.06540-11 – volume: 12 year: 2016 ident: CR24 article-title: Broadly-reactive neutralizing and non-neutralizing antibodies directed against the H7 influenza virus hemagglutinin reveal divergent mechanisms of protection publication-title: PLoS Pathog. doi: 10.1371/journal.ppat.1005578 – volume: 55 start-page: 998 year: 2022 end-page: 1012 ident: CR40 article-title: Analysis of memory B cells identifies conserved neutralizing epitopes on the N-terminal domain of variant SARS-Cov-2 spike proteins publication-title: Immunity doi: 10.1016/j.immuni.2022.04.003 – volume: 21 start-page: 73 year: 2021 end-page: 82 ident: CR105 article-title: Viral targets for vaccines against COVID-19 publication-title: Nat. Rev. Immunol. doi: 10.1038/s41577-020-00480-0 – volume: 373 start-page: eabh1766 year: 2021 ident: CR58 article-title: Ultrapotent antibodies against diverse and highly transmissible SARS-CoV-2 variants publication-title: Science doi: 10.1126/science.abh1766 – volume: 16 start-page: 1239 year: 2020 end-page: 1242 ident: CR52 article-title: Potential for developing a SARS-CoV receptor-binding domain (RBD) recombinant protein as a heterologous human vaccine against coronavirus infectious disease (COVID)-19 publication-title: Hum. Vaccin. Immunother. doi: 10.1080/21645515.2020.1740560 – volume: 86 start-page: 697 year: 2018 end-page: 706 ident: CR94 article-title: Comparative analysis of nanobody sequence and structure data publication-title: Proteins doi: 10.1002/prot.25497 – volume: 370 start-page: 1473 year: 2020 end-page: 1479 ident: CR96 article-title: An ultrapotent synthetic nanobody neutralizes SARS-CoV-2 by stabilizing inactive Spike publication-title: Science doi: 10.1126/science.abe3255 – volume: 12 year: 2021 ident: CR101 article-title: A broadly neutralizing humanized ACE2-targeting antibody against SARS-CoV-2 variants publication-title: Nat. Commun. doi: 10.1038/s41467-021-25331-x – volume: 593 start-page: 130 year: 2021 end-page: 135 ident: CR32 article-title: Antibody resistance of SARS-CoV-2 variants B.1.351 and B.1.1.7 publication-title: Nature doi: 10.1038/s41586-021-03398-2 – volume: 597 start-page: 103 year: 2021 end-page: 108 ident: CR66 article-title: Broad sarbecovirus neutralization by a human monoclonal antibody publication-title: Nature doi: 10.1038/s41586-021-03817-4 – volume: 21 start-page: 4546 year: 2020 ident: CR14 article-title: Betacoronavirus genomes: how genomic information has been used to deal with past outbreaks and the COVID-19 pandemic publication-title: Int. J. Mol. Sci. doi: 10.3390/ijms21124546 – volume: 1 start-page: 209 year: 2003 end-page: 218 ident: CR2 article-title: SARS–beginning to understand a new virus publication-title: Nat. Rev. Microbiol. doi: 10.1038/nrmicro775 – volume: 495 start-page: 251 year: 2013 end-page: 254 ident: CR18 article-title: Dipeptidyl peptidase 4 is a functional receptor for the emerging human coronavirus-EMC publication-title: Nature doi: 10.1038/nature12005 – volume: 119 year: 2022 ident: CR67 article-title: A broad and potent neutralization epitope in SARS-related coronaviruses publication-title: Proc. Natl Acad. Sci. USA doi: 10.1073/pnas.2205784119 – volume: 53 start-page: 1272 year: 2020 end-page: 1280 ident: CR70 article-title: Cross-neutralization of a SARS-CoV-2 antibody to a functionally conserved site is mediated by avidity publication-title: Immunity doi: 10.1016/j.immuni.2020.10.023 – year: 2022 ident: CR59 article-title: Patient-derived monoclonal antibody neutralizes SARS-CoV-2 Omicron variants and confers full protection in monkeys publication-title: Nat. Microbiol. doi: 10.1016/10.1038/s41564-022-01198-6 – volume: 375 start-page: 449 year: 2022 end-page: 454 ident: CR49 article-title: Antibody-mediated broad sarbecovirus neutralization through ACE2 molecular mimicry publication-title: Science doi: 10.1126/science.abm8143 – volume: 13 start-page: eabj5413 year: 2021 ident: CR98 article-title: Bispecific antibodies targeting distinct regions of the spike protein potently neutralize SARS-CoV-2 variants of concern publication-title: Sci. Transl. Med. doi: 10.1126/scitranslmed.abj5413 – volume: 12 year: 2021 ident: CR39 article-title: A combination of receptor-binding domain and N-terminal domain neutralizing antibodies limits the generation of SARS-CoV-2 spike neutralization-escape mutants publication-title: mBio doi: 10.1128/mBio.02473-21 – volume: 37 start-page: 109928 year: 2021 ident: CR34 article-title: Neutralizing antibody 5-7 defines a distinct site of vulnerability in SARS-CoV-2 spike N-terminal domain publication-title: Cell Rep. doi: 10.1016/j.celrep.2021.109928 – volume: 584 start-page: 443 year: 2020 end-page: 449 ident: CR54 article-title: Potently neutralizing and protective human antibodies against SARS-CoV-2 publication-title: Nature doi: 10.1038/s41586-020-2548-6 – volume: 9 start-page: 664 year: 2020 end-page: 675 ident: CR25 article-title: Generation of neutralizing and non-neutralizing monoclonal antibodies against H7N9 influenza virus publication-title: Emerg. Microbes Infect. doi: 10.1080/22221751.2020.1742076 – volume: 584 start-page: 450 year: 2020 end-page: 456 ident: CR29 article-title: Potent neutralizing antibodies against multiple epitopes on SARS-CoV-2 spike publication-title: Nature doi: 10.1038/s41586-020-2571-7 – volume: 597 start-page: 703 year: 2021 end-page: 708 ident: CR45 article-title: Emergence and expansion of SARS-CoV-2 B.1.526 after identification in New York publication-title: Nature doi: 10.1038/s41586-021-03908-2 – year: 2022 ident: CR60 article-title: P2G3 human monoclonal antibody neutralizes SARS-CoV-2 Omicron subvariants including BA.4 and BA.5 and Bebtelovimab escape mutants publication-title: bioRxiv doi: 10.1101/2022.07.28.501852 – volume: 377 start-page: 735 year: 2022 end-page: 742 ident: CR87 article-title: ACE2 engagement exposes the fusion peptide to pan-coronavirus neutralizing antibodies publication-title: Science doi: 10.1126/science.abq2679 – volume: 23 start-page: 423 year: 2022 end-page: 430 ident: CR100 article-title: An engineered bispecific human monoclonal antibody against SARS-CoV-2 publication-title: Nat. Immunol. doi: 10.1038/s41590-022-01138-w – volume: 29 start-page: 747 year: 2021 end-page: 751 ident: CR46 article-title: Increased resistance of SARS-CoV-2 variant P.1 to antibody neutralization publication-title: Cell Host Microbe doi: 10.1016/j.chom.2021.04.007 – year: 2022 ident: CR90 article-title: Extremely potent monoclonal antibodies neutralize Omicron and other SARS-CoV-2 variants publication-title: medRxiv doi: 10.1101/2022.01.12.22269023 – volume: 13 year: 2021 ident: CR93 article-title: Nanobody-A versatile tool for cancer diagnosis and therapeutics publication-title: Wiley Interdiscip. Rev. Nanomed. Nanobiotechnol. doi: 10.1002/wnan.1697 – volume: 10 start-page: 587269 year: 2020 ident: CR8 article-title: SARS-CoV-2: structure, biology, and structure-based therapeutics development publication-title: Front. Cell Infect. Microbiol. doi: 10.3389/fcimb.2020.587269 – volume: 27 start-page: 950 year: 2020 end-page: 958 ident: CR75 article-title: Structural basis for the neutralization of SARS-CoV-2 by an antibody from a convalescent patient publication-title: Nat. Struct. Mol. Biol. doi: 10.1038/s41594-020-0480-y – volume: 202 start-page: S315 year: 2010 end-page: S322 ident: CR26 article-title: The humoral response to HIV-1: new insights, renewed focus publication-title: J. Infect. Dis. doi: 10.1086/655654 – volume: 3 year: 2020 ident: CR20 article-title: TMPRSS2 and furin are both essential for proteolytic activation of SARS-CoV-2 in human airway cells publication-title: Life Sci. Alliance doi: 10.26508/lsa.202000786 – volume: 5 start-page: 536 year: 2020 end-page: 544 ident: CR5 article-title: The species : classifying 2019-nCoV and naming it SARS-CoV-2 publication-title: Nat. Microbiol. doi: 10.1038/s41564-020-0695-z – year: 2022 ident: CR57 article-title: LY-CoV1404 (bebtelovimab) potently neutralizes SARS-CoV-2 variants publication-title: Cell Rep. doi: 10.1016/j.celrep.2022.110812 – volume: 29 start-page: 744 year: 2021 end-page: 746 ident: CR31 article-title: An NTD supersite of attack publication-title: Cell Host Microbe doi: 10.1016/j.chom.2021.04.010 – volume: 373 start-page: 1109 year: 2021 end-page: 1116 ident: CR83 article-title: Broad betacoronavirus neutralization by a stem helix-specific human antibody publication-title: Science doi: 10.1126/science.abj3321 – year: 2022 ident: CR89 article-title: Engineering SARS-CoV-2 neutralizing antibodies for increased potency and reduced viral escape publication-title: iScience doi: 10.1016/j.isci.2022.104914 – year: 2022 ident: CR81 article-title: Evasion of neutralizing antibodies by Omicron sublineage BA.2.75 publication-title: Lancet Infect. Dis. doi: 10.1016/S1473-3099(22)00524-2 – volume: 29 start-page: 655 year: 2021 end-page: 663 ident: CR55 article-title: Structural basis for accommodation of emerging B.1.351 and B.1.1.7 variants by two potent SARS-CoV-2 neutralizing antibodies publication-title: Structure doi: 10.1016/j.str.2021.05.014 – volume: 368 start-page: 1274 year: 2020 end-page: 1278 ident: CR73 article-title: A noncompeting pair of human neutralizing antibodies block COVID-19 virus binding to its receptor ACE2 publication-title: Science doi: 10.1126/science.abc2241 – volume: 376 start-page: eabn8897 year: 2022 ident: CR48 article-title: Structural basis for potent antibody neutralization of SARS-CoV-2 variants including B.1.1.529 publication-title: Science doi: 10.1126/science.abn8897 – volume: 584 start-page: 115 year: 2020 end-page: 119 ident: CR77 article-title: Human neutralizing antibodies elicited by SARS-CoV-2 infection publication-title: Nature doi: 10.1038/s41586-020-2380-z – volume: 593 start-page: 424 year: 2021 end-page: 428 ident: CR97 article-title: Bispecific IgG neutralizes SARS-CoV-2 variants and prevents escape in mice publication-title: Nature doi: 10.1038/s41586-021-03461-y – year: 2022 ident: CR99 article-title: Engineering SARS-CoV-2 cocktail antibodies into a bispecific format improves neutralizing potency and breadth publication-title: bioRxiv doi: 10.1101/2022.02.01.478504 – volume: 377 start-page: 728 year: 2022 end-page: 735 ident: CR86 article-title: Broadly neutralizing antibodies target the coronavirus fusion peptide publication-title: Science doi: 10.1126/science.abq3773 – volume: 11 start-page: 147 year: 2022 end-page: 157 ident: CR65 article-title: A monoclonal antibody that neutralizes SARS-CoV-2 variants, SARS-CoV, and other sarbecoviruses publication-title: Emerg. Microbes Infect. doi: 10.1080/22221751.2021.2011623 – volume: 85 start-page: 104502 year: 2020 ident: CR7 article-title: From SARS to SARS-CoV-2, insights on structure, pathogenicity and immunity aspects of pandemic human coronaviruses publication-title: Infect. Genet. Evol. doi: 10.1016/j.meegid.2020.104502 – volume: 9 year: 2020 ident: CR16 article-title: Expression of the SARS-CoV-2 cell receptor gene ACE2 in a wide variety of human tissues publication-title: Infect. Dis. Poverty doi: 10.1186/s40249-020-00662-x – volume: 588 start-page: 682 year: 2020 end-page: 687 ident: CR41 article-title: SARS-CoV-2 neutralizing antibody structures inform therapeutic strategies publication-title: Nature doi: 10.1038/s41586-020-2852-1 – volume: 96 start-page: 753 year: 2020 end-page: 758 ident: CR3 article-title: Origin, transmission, diagnosis and management of coronavirus disease 2019 (COVID-19) publication-title: Postgrad. Med. J. – volume: 23 start-page: 1008 year: 2022 end-page: 1020 ident: CR103 article-title: The humoral response and antibodies against SARS-CoV-2 infection publication-title: Nat. Immunol. doi: 10.1038/s41590-022-01248-5 – volume: 41 start-page: 1141 year: 2020 end-page: 1149 ident: CR15 article-title: Structural and functional properties of SARS-CoV-2 spike protein: potential antivirus drug development for COVID-19 publication-title: Acta Pharmacol. Sin. doi: 10.1038/s41401-020-0485-4 – volume: 14 start-page: 523 year: 2016 end-page: 534 ident: CR17 article-title: SARS and MERS: recent insights into emerging coronaviruses publication-title: Nat. Rev. Microbiol. doi: 10.1038/nrmicro.2016.81 – year: 2022 ident: CR104 article-title: Sensitivity to vaccines, therapeutic antibodies, and viral entry inhibitors and advances to counter the SARS-CoV-2 Omicron variant publication-title: Clin. Microbiol. Rev. doi: 10.1128/cmr.00014-22 – volume: 579 start-page: 270 year: 2020 end-page: 273 ident: CR6 article-title: A pneumonia outbreak associated with a new coronavirus of probable bat origin publication-title: Nature doi: 10.1038/s41586-020-2012-7 – volume: 13 start-page: 202 year: 2021 ident: CR11 article-title: COVID-19: a review on the novel coronavirus disease evolution, transmission, detection, control and prevention publication-title: Viruses doi: 10.3390/v13020202 – volume: 7 start-page: 46 year: 2014 end-page: 56 ident: CR22 article-title: Protective effect of vaginal application of neutralizing and nonneutralizing inhibitory antibodies against vaginal SHIV challenge in macaques publication-title: Mucosal Immunol. doi: 10.1038/mi.2013.23 – volume: 184 start-page: 2316 year: 2021 end-page: 2331 ident: CR28 article-title: Neutralizing and protective human monoclonal antibodies recognizing the N-terminal domain of the SARS-CoV-2 spike protein publication-title: Cell doi: 10.1016/j.cell.2021.03.029 – volume: 44 start-page: 7 year: 2021 end-page: 17 ident: CR9 article-title: Neutralizing monoclonal antibodies for COVID-19 treatment and prevention publication-title: Biomed. J. doi: 10.1016/j.bj.2020.11.011 – volume: 608 start-page: 593 year: 2022 end-page: 602 ident: CR80 article-title: BA.2.12.1, BA.4 and BA.5 escape antibodies elicited by Omicron infection publication-title: Nature doi: 10.1038/s41586-022-04980-y – year: 2014 ident: CR95 article-title: Antibody structure publication-title: Microbiol. Spectr. doi: 10.1128/microbiolspec.AID-0012-2013 – volume: 384 start-page: 229 year: 2021 end-page: 237 ident: CR51 article-title: SARS-CoV-2 Neutralizing antibody LY-CoV555 in outpatients with Covid-19 publication-title: N. Engl. J. Med. doi: 10.1056/NEJMoa2029849 – volume: 602 start-page: 664 year: 2022 end-page: 670 ident: CR50 article-title: Broadly neutralizing antibodies overcome SARS-CoV-2 Omicron antigenic shift publication-title: Nature doi: 10.1038/s41586-021-04386-2 – volume: 174 start-page: 655 year: 2021 end-page: 662 ident: CR10 article-title: The proportion of SARS-CoV-2 infections that are asymptomatic: a systematic review publication-title: Ann. Intern. Med. doi: 10.7326/M20-6976 – volume: 91 start-page: e01762-16 year: 2017 ident: CR23 article-title: Broadly neutralizing antibodies display potential for prevention of HIV-1 infection of mucosal tissue superior to that of nonneutralizing antibodies publication-title: J. Virol. doi: 10.1128/JVI.01762-16 – year: 2022 ident: CR85 article-title: Vaccine-elicited murine antibody WS6 neutralizes diverse beta-coronaviruses by recognizing a helical stem supersite of vulnerability publication-title: Structure doi: 10.1016/j.str.2022.06.004 – volume: 584 start-page: 120 year: 2020 end-page: 124 ident: CR42 article-title: A human neutralizing antibody targets the receptor-binding site of SARS-CoV-2 publication-title: Nature doi: 10.1038/s41586-020-2381-y – volume: 17 start-page: 1057 year: 2021 end-page: 1064 ident: CR91 article-title: Rapid generation of potent antibodies by autonomous hypermutation in yeast publication-title: Nat. Chem. Biol. doi: 10.1038/s41589-021-00832-4 – volume: 14 start-page: eabi9215 year: 2022 ident: CR84 article-title: A human antibody reveals a conserved site on beta-coronavirus spike proteins and confers protection against SARS-CoV-2 infection publication-title: Sci. Transl. Med. doi: 10.1126/scitranslmed.abi9215 – volume: 597 start-page: 97 year: 2021 end-page: 102 ident: CR47 article-title: SARS-CoV-2 RBD antibodies that maximize breadth and resistance to escape publication-title: Nature doi: 10.1038/s41586-021-03807-6 – volume: 12 year: 2021 ident: CR43 article-title: A therapeutic neutralizing antibody targeting receptor binding domain of SARS-CoV-2 spike protein publication-title: Nat. Commun. doi: 10.1038/s41467-020-20602-5 – volume: 184 start-page: 2332 year: 2021 end-page: 2347 ident: CR33 article-title: N-terminal domain antigenic mapping reveals a site of vulnerability for SARS-CoV-2 publication-title: Cell doi: 10.1016/j.cell.2021.03.028 – volume: 12 start-page: 222 year: 2015 ident: CR1 article-title: MERS coronavirus: diagnostics, epidemiology and transmission publication-title: Virol. J. doi: 10.1186/s12985-015-0439-5 – volume: 101 start-page: 6212 year: 2004 end-page: 6216 ident: CR13 article-title: A previously undescribed coronavirus associated with respiratory disease in humans publication-title: Proc. Natl Acad. Sci. USA doi: 10.1073/pnas.0400762101 – volume: 264 start-page: 106420 year: 2020 ident: CR19 article-title: Delving deep into the structural aspects of a furin cleavage site inserted into the spike protein of SARS-CoV-2: a structural biophysical perspective publication-title: Biophys. Chem. doi: 10.1016/j.bpc.2020.106420 – volume: 29 start-page: 819 year: 2021 end-page: 833 ident: CR30 article-title: Potent SARS-CoV-2 neutralizing antibodies directed against spike N-terminal domain target a single supersite publication-title: Cell Host Microbe doi: 10.1016/j.chom.2021.03.005 – volume: 12 start-page: 752003 year: 2021 ident: CR82 article-title: Broadly-neutralizing antibodies against emerging SARS-CoV-2 variants publication-title: Front. Immunol. doi: 10.3389/fimmu.2021.752003 – volume: 32 start-page: 269 year: 2022 end-page: 287 ident: CR106 article-title: A novel STING agonist-adjuvanted pan-sarbecovirus vaccine elicits potent and durable neutralizing antibody and T cell responses in mice, rabbits and NHPs publication-title: Cell Res. doi: 10.1038/s41422-022-00612-2 – volume: 36 start-page: 109679 year: 2021 ident: CR37 article-title: The neutralization potency of anti-SARS-CoV-2 therapeutic human monoclonal antibodies is retained against viral variants publication-title: Cell Rep. doi: 10.1016/j.celrep.2021.109679 – volume: 7 start-page: 1063 year: 2022 end-page: 1074 ident: CR88 article-title: Neutralization mechanism of a human antibody with pan-coronavirus reactivity including SARS-CoV-2 publication-title: Nat. Microb. doi: 10.1038/s41564-022-01155-3 – year: 2022 ident: CR63 article-title: An Antibody from Single Human VH-rearranging Mouse Neutralizes All SARS-CoV-2 Variants Through BA.5 by Inhibiting Membrane Fusion publication-title: Sci. Immuno. doi: 10.1126/sciimmunol.add5446 – volume: 13 start-page: 1922134 year: 2021 ident: CR92 article-title: Potent SARS-CoV-2 binding and neutralization through maturation of iconic SARS-CoV-1 antibodies publication-title: MAbs doi: 10.1080/19420862.2021.1922134 – volume: 30 start-page: 1077 year: 2022 end-page: 1083 ident: CR36 article-title: Antibody evasion of SARS-CoV-2 Omicron BA.1, BA.1.1, BA.2, and BA.3 sub-lineages publication-title: Cell Host Microbe doi: 10.1016/j.chom.2022.05.001 – volume: 24 start-page: 102479 year: 2021 ident: CR38 article-title: Therapeutic antibodies, targeting the SARS-CoV-2 spike N-terminal domain, protect lethally infected K18-hACE2 mice publication-title: iScience doi: 10.1016/j.isci.2021.102479 – volume: 369 start-page: 1010 year: 2020 end-page: 1014 ident: CR53 article-title: Studies in humanized mice and convalescent humans yield a SARS-CoV-2 antibody cocktail publication-title: Science doi: 10.1126/science.abd0827 – volume: 296 start-page: 100306 year: 2021 ident: CR21 article-title: SARS-CoV-2 infects cells after viral entry via clathrin-mediated endocytosis publication-title: J. Biol. Chem. doi: 10.1016/j.jbc.2021.100306 – volume: 14 start-page: eabj7125 year: 2022 ident: CR69 article-title: A broadly cross-reactive antibody neutralizes and protects against sarbecovirus challenge in mice publication-title: Sci. Transl. Med. doi: 10.1126/scitranslmed.abj7125 – volume: 608 start-page: 603 year: 2022 end-page: 608 ident: CR61 article-title: Antibody evasion by SARS-CoV-2 Omicron subvariants BA.2.12.1, BA.4 and BA.5 publication-title: Nature doi: 10.1038/s41586-022-05053-w – volume: 369 start-page: 1505 year: 2020 ident: 784_CR71 publication-title: Science doi: 10.1126/science.abc5881 – volume: 7 start-page: 46 year: 2014 ident: 784_CR22 publication-title: Mucosal Immunol. doi: 10.1038/mi.2013.23 – volume: 85 start-page: 104502 year: 2020 ident: 784_CR7 publication-title: Infect. Genet. Evol. doi: 10.1016/j.meegid.2020.104502 – volume: 86 start-page: 3995 year: 2012 ident: 784_CR12 publication-title: J. Virol. doi: 10.1128/JVI.06540-11 – year: 2022 ident: 784_CR57 publication-title: Cell Rep. doi: 10.1016/j.celrep.2022.110812 – volume: 373 start-page: eabh1766 year: 2021 ident: 784_CR58 publication-title: Science doi: 10.1126/science.abh1766 – volume: 14 start-page: eabi9215 year: 2022 ident: 784_CR84 publication-title: Sci. Transl. Med. doi: 10.1126/scitranslmed.abi9215 – volume: 101 start-page: 6212 year: 2004 ident: 784_CR13 publication-title: Proc. Natl Acad. Sci. USA doi: 10.1073/pnas.0400762101 – volume: 37 start-page: 109928 year: 2021 ident: 784_CR34 publication-title: Cell Rep. doi: 10.1016/j.celrep.2021.109928 – volume: 174 start-page: 655 year: 2021 ident: 784_CR10 publication-title: Ann. Intern. Med. doi: 10.7326/M20-6976 – volume: 185 start-page: 1389 year: 2022 ident: 784_CR78 publication-title: Cell doi: 10.1016/j.cell.2022.03.009 – volume: 584 start-page: 443 year: 2020 ident: 784_CR54 publication-title: Nature doi: 10.1038/s41586-020-2548-6 – volume: 6 start-page: 315 year: 2022 ident: 784_CR102 publication-title: Signal. Transduct. Target. Ther. doi: 10.1038/s41392-021-00740-y – volume: 584 start-page: 437 year: 2020 ident: 784_CR74 publication-title: Nature doi: 10.1038/s41586-020-2456-9 – volume: 296 start-page: 100306 year: 2021 ident: 784_CR21 publication-title: J. Biol. Chem. doi: 10.1016/j.jbc.2021.100306 – volume: 11 start-page: 147 year: 2022 ident: 784_CR65 publication-title: Emerg. Microbes Infect. doi: 10.1080/22221751.2021.2011623 – volume: 593 start-page: 424 year: 2021 ident: 784_CR97 publication-title: Nature doi: 10.1038/s41586-021-03461-y – volume: 368 start-page: 630 year: 2020 ident: 784_CR64 publication-title: Science doi: 10.1126/science.abb7269 – volume: 14 start-page: eabj7125 year: 2022 ident: 784_CR69 publication-title: Sci. Transl. Med. doi: 10.1126/scitranslmed.abj7125 – volume: 29 start-page: 747 year: 2021 ident: 784_CR46 publication-title: Cell Host Microbe doi: 10.1016/j.chom.2021.04.007 – volume: 377 start-page: 735 year: 2022 ident: 784_CR87 publication-title: Science doi: 10.1126/science.abq2679 – volume: 13 start-page: 202 year: 2021 ident: 784_CR11 publication-title: Viruses doi: 10.3390/v13020202 – volume: 44 start-page: 7 year: 2021 ident: 784_CR9 publication-title: Biomed. J. doi: 10.1016/j.bj.2020.11.011 – year: 2022 ident: 784_CR76 publication-title: bioRxiv doi: 10.1101/2022.05.13.491770 – volume: 6 start-page: 378 year: 2021 ident: 784_CR79 publication-title: Signal. Transduct. Target. Ther. doi: 10.1038/s41392-021-00810-1 – volume: 588 start-page: 682 year: 2020 ident: 784_CR41 publication-title: Nature doi: 10.1038/s41586-020-2852-1 – volume: 55 start-page: 998 year: 2022 ident: 784_CR40 publication-title: Immunity doi: 10.1016/j.immuni.2022.04.003 – volume: 19 start-page: 141 year: 2021 ident: 784_CR4 publication-title: Nat. Rev. Microbiol. doi: 10.1038/s41579-020-00459-7 – year: 2022 ident: 784_CR63 publication-title: Sci. Immuno. doi: 10.1126/sciimmunol.add5446 – volume: 21 start-page: 4546 year: 2020 ident: 784_CR14 publication-title: Int. J. Mol. Sci. doi: 10.3390/ijms21124546 – year: 2022 ident: 784_CR81 publication-title: Lancet Infect. Dis. doi: 10.1016/S1473-3099(22)00524-2 – volume: 597 start-page: 97 year: 2021 ident: 784_CR47 publication-title: Nature doi: 10.1038/s41586-021-03807-6 – volume: 202 start-page: S315 year: 2010 ident: 784_CR26 publication-title: J. Infect. Dis. doi: 10.1086/655654 – volume: 11 start-page: 477 year: 2022 ident: 784_CR35 publication-title: Emerg. Microbes Infect. doi: 10.1080/22221751.2022.2030200 – volume: 584 start-page: 120 year: 2020 ident: 784_CR42 publication-title: Nature doi: 10.1038/s41586-020-2381-y – volume: 579 start-page: 270 year: 2020 ident: 784_CR6 publication-title: Nature doi: 10.1038/s41586-020-2012-7 – volume: 29 start-page: 819 year: 2021 ident: 784_CR30 publication-title: Cell Host Microbe doi: 10.1016/j.chom.2021.03.005 – volume: 593 start-page: 130 year: 2021 ident: 784_CR32 publication-title: Nature doi: 10.1038/s41586-021-03398-2 – volume: 384 start-page: 229 year: 2021 ident: 784_CR51 publication-title: N. Engl. J. Med. doi: 10.1056/NEJMoa2029849 – volume: 3 year: 2020 ident: 784_CR20 publication-title: Life Sci. Alliance doi: 10.26508/lsa.202000786 – volume: 24 start-page: 102479 year: 2021 ident: 784_CR38 publication-title: iScience doi: 10.1016/j.isci.2021.102479 – volume: 12 start-page: 752003 year: 2021 ident: 784_CR82 publication-title: Front. Immunol. doi: 10.3389/fimmu.2021.752003 – volume: 12 start-page: 222 year: 2015 ident: 784_CR1 publication-title: Virol. J. doi: 10.1186/s12985-015-0439-5 – volume: 13 start-page: eabj5413 year: 2021 ident: 784_CR98 publication-title: Sci. Transl. Med. doi: 10.1126/scitranslmed.abj5413 – volume: 184 start-page: 2332 year: 2021 ident: 784_CR33 publication-title: Cell doi: 10.1016/j.cell.2021.03.028 – volume: 30 start-page: 1077 year: 2022 ident: 784_CR36 publication-title: Cell Host Microbe doi: 10.1016/j.chom.2022.05.001 – volume: 37 start-page: 109771 year: 2021 ident: 784_CR44 publication-title: Cell Rep. doi: 10.1016/j.celrep.2021.109771 – volume: 369 start-page: 1010 year: 2020 ident: 784_CR53 publication-title: Science doi: 10.1126/science.abd0827 – volume: 23 start-page: 423 year: 2022 ident: 784_CR100 publication-title: Nat. Immunol. doi: 10.1038/s41590-022-01138-w – year: 2022 ident: 784_CR89 publication-title: iScience doi: 10.1016/j.isci.2022.104914 – volume: 21 start-page: 73 year: 2021 ident: 784_CR105 publication-title: Nat. Rev. Immunol. doi: 10.1038/s41577-020-00480-0 – volume: 375 start-page: 449 year: 2022 ident: 784_CR49 publication-title: Science doi: 10.1126/science.abm8143 – volume: 608 start-page: 593 year: 2022 ident: 784_CR80 publication-title: Nature doi: 10.1038/s41586-022-04980-y – volume: 29 start-page: 744 year: 2021 ident: 784_CR31 publication-title: Cell Host Microbe doi: 10.1016/j.chom.2021.04.010 – volume: 29 start-page: 655 year: 2021 ident: 784_CR55 publication-title: Structure doi: 10.1016/j.str.2021.05.014 – year: 2022 ident: 784_CR59 publication-title: Nat. Microbiol. doi: 10.1016/10.1038/s41564-022-01198-6 – volume: 17 start-page: 1057 year: 2021 ident: 784_CR91 publication-title: Nat. Chem. Biol. doi: 10.1038/s41589-021-00832-4 – volume: 495 start-page: 251 year: 2013 ident: 784_CR18 publication-title: Nature doi: 10.1038/nature12005 – volume: 16 start-page: 1239 year: 2020 ident: 784_CR52 publication-title: Hum. Vaccin. Immunother. doi: 10.1080/21645515.2020.1740560 – volume: 13 start-page: 1922134 year: 2021 ident: 784_CR92 publication-title: MAbs doi: 10.1080/19420862.2021.1922134 – volume: 96 start-page: 753 year: 2020 ident: 784_CR3 publication-title: Postgrad. Med. J. – year: 2022 ident: 784_CR85 publication-title: Structure doi: 10.1016/j.str.2022.06.004 – year: 2022 ident: 784_CR60 publication-title: bioRxiv doi: 10.1101/2022.07.28.501852 – year: 2014 ident: 784_CR95 publication-title: Microbiol. Spectr. doi: 10.1128/microbiolspec.AID-0012-2013 – volume: 23 start-page: 1008 year: 2022 ident: 784_CR103 publication-title: Nat. Immunol. doi: 10.1038/s41590-022-01248-5 – volume: 602 start-page: 664 year: 2022 ident: 784_CR50 publication-title: Nature doi: 10.1038/s41586-021-04386-2 – volume: 369 start-page: 1119 year: 2020 ident: 784_CR72 publication-title: Science doi: 10.1126/science.abd2321 – volume: 12 year: 2021 ident: 784_CR43 publication-title: Nat. Commun. doi: 10.1038/s41467-020-20602-5 – year: 2022 ident: 784_CR99 publication-title: bioRxiv doi: 10.1101/2022.02.01.478504 – volume: 584 start-page: 450 year: 2020 ident: 784_CR29 publication-title: Nature doi: 10.1038/s41586-020-2571-7 – year: 2022 ident: 784_CR62 publication-title: bioRxiv doi: 10.1101/2022.07.18.500332 – volume: 41 start-page: 1141 year: 2020 ident: 784_CR15 publication-title: Acta Pharmacol. Sin. doi: 10.1038/s41401-020-0485-4 – volume: 376 start-page: eabn8897 year: 2022 ident: 784_CR48 publication-title: Science doi: 10.1126/science.abn8897 – volume: 608 start-page: 603 year: 2022 ident: 784_CR61 publication-title: Nature doi: 10.1038/s41586-022-05053-w – volume: 119 year: 2022 ident: 784_CR67 publication-title: Proc. Natl Acad. Sci. USA doi: 10.1073/pnas.2205784119 – volume: 597 start-page: 703 year: 2021 ident: 784_CR45 publication-title: Nature doi: 10.1038/s41586-021-03908-2 – volume: 9 start-page: 664 year: 2020 ident: 784_CR25 publication-title: Emerg. Microbes Infect. doi: 10.1080/22221751.2020.1742076 – volume: 264 start-page: 106420 year: 2020 ident: 784_CR19 publication-title: Biophys. Chem. doi: 10.1016/j.bpc.2020.106420 – volume: 9 year: 2020 ident: 784_CR16 publication-title: Infect. Dis. Poverty doi: 10.1186/s40249-020-00662-x – volume: 584 start-page: 115 year: 2020 ident: 784_CR77 publication-title: Nature doi: 10.1038/s41586-020-2380-z – volume: 369 start-page: 650 year: 2020 ident: 784_CR27 publication-title: Science doi: 10.1126/science.abc6952 – volume: 12 year: 2016 ident: 784_CR24 publication-title: PLoS Pathog. doi: 10.1371/journal.ppat.1005578 – volume: 13 year: 2021 ident: 784_CR93 publication-title: Wiley Interdiscip. Rev. Nanomed. Nanobiotechnol. doi: 10.1002/wnan.1697 – volume: 12 year: 2021 ident: 784_CR101 publication-title: Nat. Commun. doi: 10.1038/s41467-021-25331-x – volume: 14 start-page: 523 year: 2016 ident: 784_CR17 publication-title: Nat. Rev. Microbiol. doi: 10.1038/nrmicro.2016.81 – volume: 12 year: 2021 ident: 784_CR39 publication-title: mBio doi: 10.1128/mBio.02473-21 – volume: 371 start-page: 823 year: 2021 ident: 784_CR68 publication-title: Science doi: 10.1126/science.abf4830 – volume: 5 start-page: 536 year: 2020 ident: 784_CR5 publication-title: Nat. Microbiol. doi: 10.1038/s41564-020-0695-z – volume: 368 start-page: 1274 year: 2020 ident: 784_CR73 publication-title: Science doi: 10.1126/science.abc2241 – volume: 583 start-page: 290 year: 2020 ident: 784_CR56 publication-title: Nature doi: 10.1038/s41586-020-2349-y – volume: 86 start-page: 697 year: 2018 ident: 784_CR94 publication-title: Proteins doi: 10.1002/prot.25497 – year: 2022 ident: 784_CR90 publication-title: medRxiv doi: 10.1101/2022.01.12.22269023 – year: 2022 ident: 784_CR104 publication-title: Clin. Microbiol. Rev. doi: 10.1128/cmr.00014-22 – volume: 370 start-page: 1473 year: 2020 ident: 784_CR96 publication-title: Science doi: 10.1126/science.abe3255 – volume: 184 start-page: 2316 year: 2021 ident: 784_CR28 publication-title: Cell doi: 10.1016/j.cell.2021.03.029 – volume: 36 start-page: 109679 year: 2021 ident: 784_CR37 publication-title: Cell Rep. doi: 10.1016/j.celrep.2021.109679 – volume: 91 start-page: e01762-16 year: 2017 ident: 784_CR23 publication-title: J. Virol. doi: 10.1128/JVI.01762-16 – volume: 10 start-page: 587269 year: 2020 ident: 784_CR8 publication-title: Front. Cell Infect. Microbiol. doi: 10.3389/fcimb.2020.587269 – volume: 7 start-page: 1063 year: 2022 ident: 784_CR88 publication-title: Nat. Microb. doi: 10.1038/s41564-022-01155-3 – volume: 1 start-page: 209 year: 2003 ident: 784_CR2 publication-title: Nat. Rev. Microbiol. doi: 10.1038/nrmicro775 – volume: 32 start-page: 269 year: 2022 ident: 784_CR106 publication-title: Cell Res. doi: 10.1038/s41422-022-00612-2 – volume: 377 start-page: 728 year: 2022 ident: 784_CR86 publication-title: Science doi: 10.1126/science.abq3773 – volume: 597 start-page: 103 year: 2021 ident: 784_CR66 publication-title: Nature doi: 10.1038/s41586-021-03817-4 – volume: 53 start-page: 1272 year: 2020 ident: 784_CR70 publication-title: Immunity doi: 10.1016/j.immuni.2020.10.023 – volume: 27 start-page: 950 year: 2020 ident: 784_CR75 publication-title: Nat. Struct. Mol. Biol. doi: 10.1038/s41594-020-0480-y – volume: 373 start-page: 1109 year: 2021 ident: 784_CR83 publication-title: Science doi: 10.1126/science.abj3321 |
SSID | ssj0016174 |
Score | 2.7115908 |
SecondaryResourceType | review_article |
Snippet | Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a recently emerged pathogenic human coronavirus that belongs to the sarbecovirus lineage of the... |
SourceID | pubmedcentral proquest pubmed crossref springer |
SourceType | Open Access Repository Aggregation Database Index Database Enrichment Source Publisher |
StartPage | 189 |
SubjectTerms | 631/250/2152/2153/1291 631/326/596/2558 631/326/596/4130 Antibodies Antibodies, Neutralizing Biomedical and Life Sciences Biomedicine Broadly Neutralizing Antibodies Coronaviruses COVID-19 COVID-19 vaccines Drug development Global economy Humans Immunology Pandemics Public health Review Review Article SARS-CoV-2 Severe acute respiratory syndrome coronavirus 2 Vaccines |
Title | Broadly neutralizing antibodies to SARS-CoV-2 and other human coronaviruses |
URI | https://link.springer.com/article/10.1038/s41577-022-00784-3 https://www.ncbi.nlm.nih.gov/pubmed/36168054 https://www.proquest.com/docview/2781036756 https://www.proquest.com/docview/2718962593 https://pubmed.ncbi.nlm.nih.gov/PMC9514166 |
Volume | 23 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV3dSxwxEB9apUWQ0l4_vNZKCn1rg5dLNrv7VOyhSItStJZ7W7KbBA9kV907Qf_6zmRzK1epL7sPyW4-Jh-_yUx-A_BZ5V55bzS3mUi4qqzmuU9xMdSJEyW5HYboDUfH-vBM_Zgm03jg1ka3yuWaGBZq21R0Rr47TjOBq22a6G-XV5yiRpF1NYbQeArrRF1GLl3ptFe4CLoHq7JKFReplPHSzEhmuy1uXFgl8mWnXVJxuboxPUCbD50m_7Gchg3p4CW8iEiS7XWifwVPXD2AZ11sydsBPD-KVvMBbHZnc6y7cvQafqLubezFLavdIhx03GEBDLt4VjbkVMjmDTvdOznlk-YPH2OCZeGeFgsB_VhFpAfmZna9aF37Bs4O9n9PDnkMqsArBGdzrkfSeisTb7UalTKrVFlqhWqGVsZ4YXJi5fLY0aUVRI9XGZPk0gmbWJs5J-VbWKub2m0Bc3LsEV1afBkiujdOjRX-IvGiQq1KD0Ese7SoIuM4Bb64KILlW2ZFJ4UCpVAEKRRyCF_6by47vo1Hc28vBVXEudcW9yNlCJ_6ZJw1ZAoxtWsWlEdkOal--It3nVz74qQWOkMkO4R0ReJ9BmLkXk2pZ-eBmRvhKgJcLPfrcmzcV-v_rXj_eCs-wAbFuO8c37ZhbX69cB8RCc3LnTDc8ZlNxA6sf98__nXyFyT4BTs |
linkProvider | ProQuest |
linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV3db9MwED9NnfiQEILyVRhgJHgCa3XsOMkDQmNs6uhaoX2gvQUntkWlKRlLCyp_FH8j5zjJVCb2tqc-2Ikb3_n8O9_5dwCvRWKFtUpSHbOQilxLmtgIjaEMDctc2mFdvWEylaNj8fkkPFmDP-1dGJdW2drE2lDrMndn5JtBFDO0tlEoP5z9oK5qlIuutiU0vFqMzfIXumzV-71PKN83QbC7c7Q9ok1VAZojOplTOeTaah5aLcUw43EuskwKxNlSKGWZShwtlcWRMs0cP1yuVJhww3SodWyMOwBFk78uOLoyPVj_uDP9ctDFLaTnfWYiEpRFnDfXdIY83qxwq8RJcNnzbl8WlK9uhZfw7eU0zX9itfUWuHsP7jbYlWx5ZbsPa6boww1fzXLZh5uTJk7fhzv-NJD4S04PYIzevtKnS1KYRX208hsHICjUWVa6NEYyL8nh1sEh3S6_0gAbNKlvhpG6hCDJHc2C-jk7X1SmegjH1zLhj6BXlIV5AsTwwCKe1fijHLW-MiIQ-IrQshz9ODkA1s5omjcc567Uxmlax9p5nHoppCiFtJZCygfwtnvmzDN8XNl7oxVU2qz2Kr3QzQG86ppxnbrgiypMuXB9WJw4ZxNf8djLtRuOSyZjxM4DiFYk3nVwHOCrLcXse80FjgAZITWO-67VjYu_9f-veHr1V7yEW6OjyX66vzcdP4PbAeI6n3a3Ab35-cI8Rxw2z140yk_g23Wvt7-DbUEZ |
linkToPdf | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV3db9MwED9NQ0xICEH56hhgJHgCq3XsOOkDQtNGtVE2IcZQ3zIntkWlKdnWFlT-NP467pykU5nY257yYCeOfR_-ne98B_BaDbzy3mhuUxFzVVjNBz5BZahjJ3IKOwzVGw4O9d6x-jSOx2vwp70LQ2GVrU4MitpWBZ2R96IkFahtk1j3fBMW8WV3-OHsnFMFKfK0tuU0ahYZucUvNN-m7_d3kdZvomj48dvOHm8qDPACkcqM67603srYW636uUwLledaIebWyhgvzIBSVHkcNbeCcsUVxsQD6YSNrU2do8NQVP-3EhkLkrFkvDT2yGwIHm2VKC4SKZsLO32Z9qa4aeJyUBw97dCKy9VN8QrSvRqw-Y_XNmyGw_twr0GxbLtmuwew5soO3K7rWi46sHHQeOw7cLc-F2T1daeHMEK739jTBSvdPByy_MYBGJJ3klcU0MhmFTva_nrEd6rvPMIGy8IdMRaKCbKCEi6Yn5OL-dRNH8HxjSz3Y1gvq9I9BeZk5BHZWnwYSrJvnIoUfiL2okCLTndBtCuaFU22cyq6cZoFr7tMs5oKGVIhC1TIZBfeLt85q3N9XNt7qyVU1sj9NLvk0i68WjajxJIbxpSumlMfkQ7I7MRPPKnpuhxOaqFTRNFdSFYovuxA2cBXW8rJj5AVHKEygmsc913LG5e_9f9ZbF4_i5ewgVKWfd4_HD2DOxECvDr-bgvWZxdz9xwB2Sx_ETifwclNi9pfIotD6Q |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Broadly+neutralizing+antibodies+to+SARS-CoV-2+and+other+human+coronaviruses&rft.jtitle=Nature+reviews.+Immunology&rft.au=Chen%2C+Yanjia&rft.au=Zhao%2C+Xiaoyu&rft.au=Zhou%2C+Hao&rft.au=Zhu%2C+Huanzhang&rft.date=2023-03-01&rft.issn=1474-1741&rft.eissn=1474-1741&rft.volume=23&rft.issue=3&rft.spage=189&rft_id=info:doi/10.1038%2Fs41577-022-00784-3&rft.externalDBID=NO_FULL_TEXT |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1474-1733&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1474-1733&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1474-1733&client=summon |