Anti-SARS-CoV-2 IgG antibody response among Indian COVID-19 patients using β-propiolactone-inactivated, whole virus-based indirect ELISA
•Development of indirect IgG ELISA using β-propiolactone-inactivated SARS-CoV-2.•Detection of anti-SARS-CoV-2 IgG during early disease phase.•Higher IgG seropositivity and OD values in COVID-19 patients with severe disease. Coronavirus disease 2019 (COVID-19) pandemic caused by infection with severe...
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Published in | Journal of virological methods Vol. 287; p. 113996 |
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Language | English |
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01.01.2021
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Abstract | •Development of indirect IgG ELISA using β-propiolactone-inactivated SARS-CoV-2.•Detection of anti-SARS-CoV-2 IgG during early disease phase.•Higher IgG seropositivity and OD values in COVID-19 patients with severe disease.
Coronavirus disease 2019 (COVID-19) pandemic caused by infection with severe acute respiratory syndrome – coronavirus-2 (SARS-CoV-2) continues to affect many countries and large populations. Serologic assays for antibody detection aid patient diagnosis and seroepidemiologic investigations.
An indirect IgG ELISA was developed indigenously using β-propiolactone (BPL) inactivated SARS-CoV-2. This assay was used for screening 200 healthy donor sera collected prior to COVID-19 emergence (2017–2019), 185 serum/plasma samples of confirmed COVID-19 patients (n = 137) and 57 samples of viral RNA positive asymptomatic contacts (n = 51). The IgG response was studied in relation to duration and severity of illness.
The ELISA demonstrated 97 % specificity and IgG detection in >50 %, 80 %, 93.8 % and 100 % of the patients respectively during the first, second, third and fourth week of illness. IgG detection rate was higher in patients with severe disease (SD, 90.9 %) than those with mild disease (MD, 68.8 %) during the second week of illness (P = 0.027). IgG seropositivity among asymptomatic contacts was 64.7 %. IgG ELISA absorbance values were higher in SD than MD patients during the first 2 weeks of illness (P < 0.05). No significant difference was observed between the absorbance values of asymptomatic subjects and MD patients (P = 0.94).
The BPL inactivated virus-based ELISA could detect IgG antibodies early and in a significant proportion of COVID-19 patients suggesting its potential utility as a supplement to the currently used viral RNA detection tests in patient diagnosis and contact screening algorithms. |
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AbstractList | •
Development of indirect IgG ELISA using β-propiolactone-inactivated SARS-CoV-2.
•
Detection of anti-SARS-CoV-2 IgG during early disease phase.
•
Higher IgG seropositivity and OD values in COVID-19 patients with severe disease. Coronavirus disease 2019 (COVID-19) pandemic caused by infection with severe acute respiratory syndrome - coronavirus-2 (SARS-CoV-2) continues to affect many countries and large populations. Serologic assays for antibody detection aid patient diagnosis and seroepidemiologic investigations. An indirect IgG ELISA was developed indigenously using β-propiolactone (BPL) inactivated SARS-CoV-2. This assay was used for screening 200 healthy donor sera collected prior to COVID-19 emergence (2017-2019), 185 serum/plasma samples of confirmed COVID-19 patients (n = 137) and 57 samples of viral RNA positive asymptomatic contacts (n = 51). The IgG response was studied in relation to duration and severity of illness. The ELISA demonstrated 97 % specificity and IgG detection in >50 %, 80 %, 93.8 % and 100 % of the patients respectively during the first, second, third and fourth week of illness. IgG detection rate was higher in patients with severe disease (SD, 90.9 %) than those with mild disease (MD, 68.8 %) during the second week of illness (P = 0.027). IgG seropositivity among asymptomatic contacts was 64.7 %. IgG ELISA absorbance values were higher in SD than MD patients during the first 2 weeks of illness (P < 0.05). No significant difference was observed between the absorbance values of asymptomatic subjects and MD patients (P = 0.94). The BPL inactivated virus-based ELISA could detect IgG antibodies early and in a significant proportion of COVID-19 patients suggesting its potential utility as a supplement to the currently used viral RNA detection tests in patient diagnosis and contact screening algorithms. •Development of indirect IgG ELISA using β-propiolactone-inactivated SARS-CoV-2.•Detection of anti-SARS-CoV-2 IgG during early disease phase.•Higher IgG seropositivity and OD values in COVID-19 patients with severe disease. Coronavirus disease 2019 (COVID-19) pandemic caused by infection with severe acute respiratory syndrome – coronavirus-2 (SARS-CoV-2) continues to affect many countries and large populations. Serologic assays for antibody detection aid patient diagnosis and seroepidemiologic investigations. An indirect IgG ELISA was developed indigenously using β-propiolactone (BPL) inactivated SARS-CoV-2. This assay was used for screening 200 healthy donor sera collected prior to COVID-19 emergence (2017–2019), 185 serum/plasma samples of confirmed COVID-19 patients (n = 137) and 57 samples of viral RNA positive asymptomatic contacts (n = 51). The IgG response was studied in relation to duration and severity of illness. The ELISA demonstrated 97 % specificity and IgG detection in >50 %, 80 %, 93.8 % and 100 % of the patients respectively during the first, second, third and fourth week of illness. IgG detection rate was higher in patients with severe disease (SD, 90.9 %) than those with mild disease (MD, 68.8 %) during the second week of illness (P = 0.027). IgG seropositivity among asymptomatic contacts was 64.7 %. IgG ELISA absorbance values were higher in SD than MD patients during the first 2 weeks of illness (P < 0.05). No significant difference was observed between the absorbance values of asymptomatic subjects and MD patients (P = 0.94). The BPL inactivated virus-based ELISA could detect IgG antibodies early and in a significant proportion of COVID-19 patients suggesting its potential utility as a supplement to the currently used viral RNA detection tests in patient diagnosis and contact screening algorithms. Coronavirus disease 2019 (COVID-19) pandemic caused by infection with severe acute respiratory syndrome – coronavirus-2 (SARS-CoV-2) continues to affect many countries and large populations. Serologic assays for antibody detection aid patient diagnosis and seroepidemiologic investigations.An indirect IgG ELISA was developed indigenously using β-propiolactone (BPL) inactivated SARS-CoV-2. This assay was used for screening 200 healthy donor sera collected prior to COVID-19 emergence (2017–2019), 185 serum/plasma samples of confirmed COVID-19 patients (n = 137) and 57 samples of viral RNA positive asymptomatic contacts (n = 51). The IgG response was studied in relation to duration and severity of illness.The ELISA demonstrated 97 % specificity and IgG detection in >50 %, 80 %, 93.8 % and 100 % of the patients respectively during the first, second, third and fourth week of illness. IgG detection rate was higher in patients with severe disease (SD, 90.9 %) than those with mild disease (MD, 68.8 %) during the second week of illness (P = 0.027). IgG seropositivity among asymptomatic contacts was 64.7 %. IgG ELISA absorbance values were higher in SD than MD patients during the first 2 weeks of illness (P < 0.05). No significant difference was observed between the absorbance values of asymptomatic subjects and MD patients (P = 0.94).The BPL inactivated virus-based ELISA could detect IgG antibodies early and in a significant proportion of COVID-19 patients suggesting its potential utility as a supplement to the currently used viral RNA detection tests in patient diagnosis and contact screening algorithms. Coronavirus disease 2019 (COVID-19) pandemic caused by infection with severe acute respiratory syndrome - coronavirus-2 (SARS-CoV-2) continues to affect many countries and large populations. Serologic assays for antibody detection aid patient diagnosis and seroepidemiologic investigations.BACKGROUNDCoronavirus disease 2019 (COVID-19) pandemic caused by infection with severe acute respiratory syndrome - coronavirus-2 (SARS-CoV-2) continues to affect many countries and large populations. Serologic assays for antibody detection aid patient diagnosis and seroepidemiologic investigations.An indirect IgG ELISA was developed indigenously using β-propiolactone (BPL) inactivated SARS-CoV-2. This assay was used for screening 200 healthy donor sera collected prior to COVID-19 emergence (2017-2019), 185 serum/plasma samples of confirmed COVID-19 patients (n = 137) and 57 samples of viral RNA positive asymptomatic contacts (n = 51). The IgG response was studied in relation to duration and severity of illness.METHODSAn indirect IgG ELISA was developed indigenously using β-propiolactone (BPL) inactivated SARS-CoV-2. This assay was used for screening 200 healthy donor sera collected prior to COVID-19 emergence (2017-2019), 185 serum/plasma samples of confirmed COVID-19 patients (n = 137) and 57 samples of viral RNA positive asymptomatic contacts (n = 51). The IgG response was studied in relation to duration and severity of illness.The ELISA demonstrated 97 % specificity and IgG detection in >50 %, 80 %, 93.8 % and 100 % of the patients respectively during the first, second, third and fourth week of illness. IgG detection rate was higher in patients with severe disease (SD, 90.9 %) than those with mild disease (MD, 68.8 %) during the second week of illness (P = 0.027). IgG seropositivity among asymptomatic contacts was 64.7 %. IgG ELISA absorbance values were higher in SD than MD patients during the first 2 weeks of illness (P < 0.05). No significant difference was observed between the absorbance values of asymptomatic subjects and MD patients (P = 0.94).RESULTSThe ELISA demonstrated 97 % specificity and IgG detection in >50 %, 80 %, 93.8 % and 100 % of the patients respectively during the first, second, third and fourth week of illness. IgG detection rate was higher in patients with severe disease (SD, 90.9 %) than those with mild disease (MD, 68.8 %) during the second week of illness (P = 0.027). IgG seropositivity among asymptomatic contacts was 64.7 %. IgG ELISA absorbance values were higher in SD than MD patients during the first 2 weeks of illness (P < 0.05). No significant difference was observed between the absorbance values of asymptomatic subjects and MD patients (P = 0.94).The BPL inactivated virus-based ELISA could detect IgG antibodies early and in a significant proportion of COVID-19 patients suggesting its potential utility as a supplement to the currently used viral RNA detection tests in patient diagnosis and contact screening algorithms.CONCLUSIONThe BPL inactivated virus-based ELISA could detect IgG antibodies early and in a significant proportion of COVID-19 patients suggesting its potential utility as a supplement to the currently used viral RNA detection tests in patient diagnosis and contact screening algorithms. |
ArticleNumber | 113996 |
Author | Kulkarni, Ruta Mishra, Akhilesh Chandra Arankalle, Vidya Lalwani, Sanjay Palkar, Sonali Patil, Harshad P. |
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CitedBy_id | crossref_primary_10_1371_journal_pone_0246346 crossref_primary_10_1016_j_trac_2023_117291 crossref_primary_10_1016_j_talanta_2022_123409 crossref_primary_10_3390_pr11010194 crossref_primary_10_1007_s15010_021_01650_5 crossref_primary_10_1021_acs_analchem_2c01087 crossref_primary_10_1016_j_biosx_2022_100278 crossref_primary_10_1002_iid3_402 crossref_primary_10_1080_03772063_2023_2205836 crossref_primary_10_4103_ijmr_IJMR_3806_20 crossref_primary_10_22159_ijap_2025v17i2_52098 crossref_primary_10_1089_vim_2020_0321 crossref_primary_10_1016_j_ijcce_2021_04_001 crossref_primary_10_3389_fimmu_2021_733539 |
Cites_doi | 10.1016/S1473-3099(20)30196-1 10.1093/infdis/jiaa229 10.1080/22221751.2020.1729071 10.1016/j.cmi.2020.05.023 10.1080/22221751.2020.1773324 10.1080/22221751.2020.1762515 10.1016/j.jcv.2020.104529 10.1080/14737159.2020.1757437 10.1038/s41591-020-0897-1 |
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Keywords | COVID-19 IgG SARS-CoV-2 Inactivated virus Antibody ELISA |
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References | Zhang, Du RH, Zheng, Yang, Hu, Wang, Xiao, Yan, Shi, Zhou (bib0105) 2020; 9 Tahamtan, Ardebili (bib0070) 2020; 20 Van Elslande, Houben, Depypere, Brackenier, Desmet, André, Van Ranst, Lagrou, Vermeersch (bib0080) 2020; 26 World Health Organization. Liu, Wang, Xu, Liao, Chen, Hu (bib0030) 2020; 9 Guo, Ren, Yang, Xiao, Chang, Yang, Dela Cruz, Wang, Wu, Xiao, Zhang, Han, Dang, Xu, Yang, Xu, Zhu, Xu, Jin, Sharma, Wang, Wang (bib0005) 2020 Zhao, Yuan, Wang, Liu, Liao, Su, Wang, Yuan, Li, Li, Qian, Hong, Wang, Liu, Wang, He, Li, He, Zhang, Fu, Ge, Liu, Zhang, Xia, Zhang (bib0010) 2020 Sapkal, Shete-Aich, Jain, Yadav, Sarkale, Lakra, Baradkar, Deshpande, Mali, Tilekar, Majumdar, Kaushal, Gurav, Gupta, Mohandas, Deshpande, Kaduskar, Salve, Patil, Gaikwad, Sugunan, Ashok, Giri, Shastri, Abraham, Gangakhedkar (bib0055) 2020; 151 Sun, Feng, Mo, Zheng, Wang, Li, Peng, Liu, Chen, Huang, Zhang, Luo, Niu, Hu, Wang, Peng, Huang, Feng, Li, Zhang, Li, Zhong, Chen (bib0065) 2020; 9 Liu, Liu, Kou, Zheng, Ding, Ni, Wang, Tan, Wu, Tang, Xiong, Zheng (bib0025) 2020; 58 Long, Tang, Shi, Li, Deng, Yuan, Hu, Xu, Zhang, Lv, Su, Zhang, Gong, Wu, Liu, Li, Qiu, Chen, Huang (bib0040) 2020 Kohmer, Westhaus, Rühl, Ciesek, Rabenau (bib0020) 2020 World Health Organization (bib0090) 2020 Wu, Tseng, Lin, Lee, Chung, Huang, Chen, Hsueh, Chen (bib0095) 2020 2020 (accessed 22 July 2020). Serrano, Rodríguez, Palop, Arenas, Córdoba, Mochón, Cardona (bib0060) 2020; 129 Perera, Mok, Tsang, Lv, Ko, Wu, Yuan, Leung, Chan, Chik, Choi, Leung, Chan, Chan, Li, Wu, Wilson, Monto, Poon, Peiris (bib0045) 2020; 25 Kohmer, Westhaus, Rühl, Ciesek, Rabenau (bib0015) 2020 To, Tsang, Leung, Tam, Wu, Lung, Yip, Cai, Chan, Chik, Lau, Choi, Chen, Chan, Chan, Ip, Ng, Poon, Luo, Cheng, Chan, Hung, Chen, Chen, Yuen (bib0075) 2020; 20 Zhao, Li, Song, Chen, Ren, Feng, Gao, Song, Peng, Su, Guo, Wang, Chen, Li, Sun, Bai, Cao, Zhu, Zhang, Sun, Sun, Mao, Su, Chen, He, Gao, Jin, Jiang, Sun (bib0050) 2020 Long, Liu, Deng, Wu, Deng, Chen, Liao, Qiu, Lin, Cai, Wang, Hu, Ren, Tang, Xu, Yu LH, Gong, Zhang, Tian, Hu, Zhang, Xiang, Du HX, Lang, Luo, Wu, Cui, Zhou, Zhu, Wang, Xue, Li, Wang, Li, Wang, Niu, Yang, Tang, Zhang, Liu, Li, Zhang, Zhang, Liu, Yuan, Li, Hu, Chen, Huang (bib0035) 2020; 26 Zhang, Nie, Zhang, Zhang (bib0100) 2020; 222 To (10.1016/j.jviromet.2020.113996_bib0075) 2020; 20 Zhao (10.1016/j.jviromet.2020.113996_bib0050) 2020 Zhang (10.1016/j.jviromet.2020.113996_bib0100) 2020; 222 Guo (10.1016/j.jviromet.2020.113996_bib0005) 2020 Liu (10.1016/j.jviromet.2020.113996_bib0030) 2020; 9 Tahamtan (10.1016/j.jviromet.2020.113996_bib0070) 2020; 20 Zhang (10.1016/j.jviromet.2020.113996_bib0105) 2020; 9 Zhao (10.1016/j.jviromet.2020.113996_bib0010) 2020 Sapkal (10.1016/j.jviromet.2020.113996_bib0055) 2020; 151 Sun (10.1016/j.jviromet.2020.113996_bib0065) 2020; 9 Serrano (10.1016/j.jviromet.2020.113996_bib0060) 2020; 129 Long (10.1016/j.jviromet.2020.113996_bib0040) 2020 Perera (10.1016/j.jviromet.2020.113996_bib0045) 2020; 25 10.1016/j.jviromet.2020.113996_bib0085 Liu (10.1016/j.jviromet.2020.113996_bib0025) 2020; 58 Wu (10.1016/j.jviromet.2020.113996_bib0095) 2020 Kohmer (10.1016/j.jviromet.2020.113996_bib0015) 2020 Kohmer (10.1016/j.jviromet.2020.113996_bib0020) 2020 Van Elslande (10.1016/j.jviromet.2020.113996_bib0080) 2020; 26 World Health Organization (10.1016/j.jviromet.2020.113996_bib0090) 2020 Long (10.1016/j.jviromet.2020.113996_bib0035) 2020; 26 |
References_xml | – volume: 25 start-page: 2000421 year: 2020 ident: bib0045 article-title: Serological assays for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), March 2020 publication-title: Euro Surveill. – volume: 151 start-page: 444 year: 2020 end-page: 449 ident: bib0055 article-title: Development of indigenous IgG ELISA for the detection of anti-SARS-CoV-2 IgG publication-title: Indian J. Med. Res. – start-page: 8 year: 2020 ident: bib0020 article-title: Clinical performance of different SARS-CoV-2 IgG antibody tests publication-title: J. Med. Virol. – volume: 222 start-page: 183 year: 2020 end-page: 188 ident: bib0100 article-title: Longitudinal Change of Severe Acute Respiratory Syndrome Coronavirus 2 Antibodies in Patients with Coronavirus Disease 2019 publication-title: J. Infect. Dis. – reference: /, 2020 (accessed 22 July 2020). – volume: 9 start-page: 386 year: 2020 end-page: 389 ident: bib0105 article-title: Molecular and serological investigation of 2019-nCoV infected patients: implication of multiple shedding routes publication-title: Emerg. Microbes Infect. – volume: 20 start-page: 453 year: 2020 end-page: 454 ident: bib0070 article-title: Real-time RT-PCR in COVID-19 detection: issues affecting the results publication-title: Expert Rev. Mol. Diagn. – start-page: 15 year: 2020 ident: bib0095 article-title: Four point-of-care lateral flow immunoassays for diagnosis of COVID-19 and for assessing dynamics of antibody responses to SARS-CoV-2 publication-title: J. Infect. – volume: 9 start-page: 1269 year: 2020 end-page: 1274 ident: bib0030 article-title: Patterns of IgG and IgM antibody response in COVID-19 patients publication-title: Emerg. Microbes Infect. – volume: 58 year: 2020 ident: bib0025 article-title: Evaluation of Nucleocapsid and Spike protein-based enzyme-linked immunosorbent assays for detecting antibodies against SARS-CoV-2 publication-title: J. Clin. Microbiol. – start-page: 18 year: 2020 ident: bib0040 article-title: Clinical and immunological assessment of asymptomatic SARS-CoV-2 infections publication-title: Nat. Med. – volume: 20 start-page: 565 year: 2020 end-page: 574 ident: bib0075 article-title: Temporal profiles of viral load in posterior oropharyngeal saliva samples and serum antibody responses during infection by SARS-CoV-2: an observational cohort study publication-title: Lancet Infect. Dis. – volume: 129 start-page: 104529 year: 2020 ident: bib0060 article-title: Comparison of commercial lateral flow immunoassays and ELISA for SARS-CoV-2 antibody detection publication-title: J. Clin. Virol. – year: 2020 ident: bib0090 article-title: Laboratory Testing for Coronavirus Disease (COVID-19) in Suspected Human Cases: Interim Guidance – year: 2020 ident: bib0050 article-title: Early detection of SARS-CoV-2 antibodies in COVID-19 patients as a serologic marker of infection publication-title: Clin. Infect. Dis. – volume: 9 start-page: 940 year: 2020 end-page: 948 ident: bib0065 article-title: Kinetics of SARS-CoV-2 specific IgM and IgG responses in COVID-19 patients publication-title: Emerg. Microbes Infect. – volume: 26 start-page: 845 year: 2020 end-page: 848 ident: bib0035 article-title: Antibody responses to SARS-CoV-2 in patients with COVID-19 publication-title: Nat. Med. – reference: World Health Organization. – start-page: 129 year: 2020 ident: bib0015 article-title: Brief clinical evaluation of six high-throughput SARS-CoV-2 IgG antibody assays publication-title: J. Clin. Virol. – start-page: 21 year: 2020 ident: bib0005 article-title: Profiling early humoral response to diagnose novel coronavirus disease (COVID-19) publication-title: Clin. Infect. Dis. – start-page: 28 year: 2020 ident: bib0010 article-title: Antibody responses to SARS-CoV-2 in patients of novel coronavirus disease 2019 publication-title: Clin. Infect. Dis. – volume: 26 start-page: 1082 year: 2020 end-page: 1087 ident: bib0080 article-title: Diagnostic performance of seven rapid IgG/IgM antibody tests and the Euroimmun IgA/IgG ELISA in COVID-19 patients publication-title: Clin. Microbiol. Infect. – start-page: 18 issue: June year: 2020 ident: 10.1016/j.jviromet.2020.113996_bib0040 article-title: Clinical and immunological assessment of asymptomatic SARS-CoV-2 infections publication-title: Nat. Med. – start-page: 28 issue: March year: 2020 ident: 10.1016/j.jviromet.2020.113996_bib0010 article-title: Antibody responses to SARS-CoV-2 in patients of novel coronavirus disease 2019 publication-title: Clin. Infect. Dis. – volume: 20 start-page: 565 issue: May(5) year: 2020 ident: 10.1016/j.jviromet.2020.113996_bib0075 article-title: Temporal profiles of viral load in posterior oropharyngeal saliva samples and serum antibody responses during infection by SARS-CoV-2: an observational cohort study publication-title: Lancet Infect. Dis. doi: 10.1016/S1473-3099(20)30196-1 – volume: 222 start-page: 183 issue: June (2) year: 2020 ident: 10.1016/j.jviromet.2020.113996_bib0100 article-title: Longitudinal Change of Severe Acute Respiratory Syndrome Coronavirus 2 Antibodies in Patients with Coronavirus Disease 2019 publication-title: J. Infect. Dis. doi: 10.1093/infdis/jiaa229 – volume: 9 start-page: 386 issue: February (1) year: 2020 ident: 10.1016/j.jviromet.2020.113996_bib0105 article-title: Molecular and serological investigation of 2019-nCoV infected patients: implication of multiple shedding routes publication-title: Emerg. Microbes Infect. doi: 10.1080/22221751.2020.1729071 – volume: 58 issue: May (6) year: 2020 ident: 10.1016/j.jviromet.2020.113996_bib0025 article-title: Evaluation of Nucleocapsid and Spike protein-based enzyme-linked immunosorbent assays for detecting antibodies against SARS-CoV-2 publication-title: J. Clin. Microbiol. – issue: May year: 2020 ident: 10.1016/j.jviromet.2020.113996_bib0050 article-title: Early detection of SARS-CoV-2 antibodies in COVID-19 patients as a serologic marker of infection publication-title: Clin. Infect. Dis. – start-page: 15 issue: June year: 2020 ident: 10.1016/j.jviromet.2020.113996_bib0095 article-title: Four point-of-care lateral flow immunoassays for diagnosis of COVID-19 and for assessing dynamics of antibody responses to SARS-CoV-2 publication-title: J. Infect. – volume: 26 start-page: 1082 issue: August(8) year: 2020 ident: 10.1016/j.jviromet.2020.113996_bib0080 article-title: Diagnostic performance of seven rapid IgG/IgM antibody tests and the Euroimmun IgA/IgG ELISA in COVID-19 patients publication-title: Clin. Microbiol. Infect. doi: 10.1016/j.cmi.2020.05.023 – volume: 9 start-page: 1269 issue: December(1) year: 2020 ident: 10.1016/j.jviromet.2020.113996_bib0030 article-title: Patterns of IgG and IgM antibody response in COVID-19 patients publication-title: Emerg. Microbes Infect. doi: 10.1080/22221751.2020.1773324 – start-page: 129 issue: June year: 2020 ident: 10.1016/j.jviromet.2020.113996_bib0015 article-title: Brief clinical evaluation of six high-throughput SARS-CoV-2 IgG antibody assays publication-title: J. Clin. Virol. – start-page: 8 issue: June year: 2020 ident: 10.1016/j.jviromet.2020.113996_bib0020 article-title: Clinical performance of different SARS-CoV-2 IgG antibody tests publication-title: J. Med. Virol. – volume: 25 start-page: 2000421 issue: April(16) year: 2020 ident: 10.1016/j.jviromet.2020.113996_bib0045 article-title: Serological assays for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), March 2020 publication-title: Euro Surveill. – volume: 9 start-page: 940 issue: December(1) year: 2020 ident: 10.1016/j.jviromet.2020.113996_bib0065 article-title: Kinetics of SARS-CoV-2 specific IgM and IgG responses in COVID-19 patients publication-title: Emerg. Microbes Infect. doi: 10.1080/22221751.2020.1762515 – volume: 151 start-page: 444 issue: May(5) year: 2020 ident: 10.1016/j.jviromet.2020.113996_bib0055 article-title: Development of indigenous IgG ELISA for the detection of anti-SARS-CoV-2 IgG publication-title: Indian J. Med. Res. – year: 2020 ident: 10.1016/j.jviromet.2020.113996_bib0090 – start-page: 21 issue: March year: 2020 ident: 10.1016/j.jviromet.2020.113996_bib0005 article-title: Profiling early humoral response to diagnose novel coronavirus disease (COVID-19) publication-title: Clin. Infect. Dis. – volume: 129 start-page: 104529 issue: June year: 2020 ident: 10.1016/j.jviromet.2020.113996_bib0060 article-title: Comparison of commercial lateral flow immunoassays and ELISA for SARS-CoV-2 antibody detection publication-title: J. Clin. Virol. doi: 10.1016/j.jcv.2020.104529 – ident: 10.1016/j.jviromet.2020.113996_bib0085 – volume: 20 start-page: 453 issue: May(5) year: 2020 ident: 10.1016/j.jviromet.2020.113996_bib0070 article-title: Real-time RT-PCR in COVID-19 detection: issues affecting the results publication-title: Expert Rev. Mol. Diagn. doi: 10.1080/14737159.2020.1757437 – volume: 26 start-page: 845 issue: June(6) year: 2020 ident: 10.1016/j.jviromet.2020.113996_bib0035 article-title: Antibody responses to SARS-CoV-2 in patients with COVID-19 publication-title: Nat. Med. doi: 10.1038/s41591-020-0897-1 |
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Snippet | •Development of indirect IgG ELISA using β-propiolactone-inactivated SARS-CoV-2.•Detection of anti-SARS-CoV-2 IgG during early disease phase.•Higher IgG... Coronavirus disease 2019 (COVID-19) pandemic caused by infection with severe acute respiratory syndrome - coronavirus-2 (SARS-CoV-2) continues to affect many... Coronavirus disease 2019 (COVID-19) pandemic caused by infection with severe acute respiratory syndrome – coronavirus-2 (SARS-CoV-2) continues to affect many... • Development of indirect IgG ELISA using β-propiolactone-inactivated SARS-CoV-2. • Detection of anti-SARS-CoV-2 IgG during early disease phase. • Higher IgG... |
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SubjectTerms | absorbance Antibodies, Viral - blood Antibody antibody detection antibody formation blood serum COVID-19 COVID-19 - blood COVID-19 - diagnosis COVID-19 - pathology COVID-19 infection COVID-19 Serological Testing - methods disease severity ELISA Enzyme-Linked Immunosorbent Assay Humans IgG Immunoglobulin G - blood Inactivated virus pandemic patients Propiolactone - pharmacology RNA SARS-CoV-2 SARS-CoV-2 - immunology Sensitivity and Specificity Seroepidemiologic Studies seroprevalence Severe acute respiratory syndrome coronavirus 2 Virus Inactivation - drug effects |
Title | Anti-SARS-CoV-2 IgG antibody response among Indian COVID-19 patients using β-propiolactone-inactivated, whole virus-based indirect ELISA |
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