Antibodies to the Spike Protein Receptor-Binding Domain of SARS-CoV-2 at 4–13 Months after COVID-19
Identification of factors behind the level and duration of persistence of the SARS-CoV-2 antibodies in the blood is assumed to set the direction for studying humoral immunity mechanisms against COVID-19, optimizing the strategy for vaccine use, antibody-based drugs, and epidemiological control of CO...
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Published in | Journal of clinical medicine Vol. 11; no. 14; p. 4053 |
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Main Authors | , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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13.07.2022
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Abstract | Identification of factors behind the level and duration of persistence of the SARS-CoV-2 antibodies in the blood is assumed to set the direction for studying humoral immunity mechanisms against COVID-19, optimizing the strategy for vaccine use, antibody-based drugs, and epidemiological control of COVID-19. Objective: This study aimed to study the relationship between clinical and demographic characteristics and the level of IgG antibodies to the RBD of SARS-CoV-2 spike protein after COVID-19 in the long term. Residents of the Altai Region of Western Siberia of Russia, Caucasians, aged from 27 to 93 years (median 53.0 years), who recovered from COVID-19 between May 2020 and February 2021 (n = 44) took part in this prospective observational study. The titer of IgG antibodies to the RBD of SARS-CoV-2 spike protein was measured repeatedly in the blood at 4–13 months from the beginning of the clinical manifestation of COVID-19 via the method of enzyme-linked immunosorbent assay. The antibody titer positively correlated with age (p = 0.013) and COVID-19 pneumonia (p = 0.002) at 20–40 and 20–24 weeks from the onset of COVID-19 symptoms, respectively. Age was positively associated with antibody titer regardless of history of COVID-19 pneumonia (beta regression coefficient p = 0.009). The antibody titer decreased in 15 (34.1%) patients, increased in 10 (22.7%) patients, and did not change in 19 (43.2%) patients from the baseline to 48–49 weeks from the onset of COVID-19 symptoms, with seropositivity persisting in all patients. Age and COVID-19 pneumonia are possibly associated with higher IgG antibodies to the spike protein RBD of SARS-CoV-2 following COVID-19 in the long term. Divergent trends of anti-RBD IgG levels in adults illustrate inter-individual differences at 4–13 months from the onset of COVID-19 symptoms. |
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AbstractList | Identification of factors behind the level and duration of persistence of the SARS-CoV-2 antibodies in the blood is assumed to set the direction for studying humoral immunity mechanisms against COVID-19, optimizing the strategy for vaccine use, antibody-based drugs, and epidemiological control of COVID-19. Objective: This study aimed to study the relationship between clinical and demographic characteristics and the level of IgG antibodies to the RBD of SARS-CoV-2 spike protein after COVID-19 in the long term. Residents of the Altai Region of Western Siberia of Russia, Caucasians, aged from 27 to 93 years (median 53.0 years), who recovered from COVID-19 between May 2020 and February 2021 (n = 44) took part in this prospective observational study. The titer of IgG antibodies to the RBD of SARS-CoV-2 spike protein was measured repeatedly in the blood at 4–13 months from the beginning of the clinical manifestation of COVID-19 via the method of enzyme-linked immunosorbent assay. The antibody titer positively correlated with age (p = 0.013) and COVID-19 pneumonia (p = 0.002) at 20–40 and 20–24 weeks from the onset of COVID-19 symptoms, respectively. Age was positively associated with antibody titer regardless of history of COVID-19 pneumonia (beta regression coefficient p = 0.009). The antibody titer decreased in 15 (34.1%) patients, increased in 10 (22.7%) patients, and did not change in 19 (43.2%) patients from the baseline to 48–49 weeks from the onset of COVID-19 symptoms, with seropositivity persisting in all patients. Age and COVID-19 pneumonia are possibly associated with higher IgG antibodies to the spike protein RBD of SARS-CoV-2 following COVID-19 in the long term. Divergent trends of anti-RBD IgG levels in adults illustrate inter-individual differences at 4–13 months from the onset of COVID-19 symptoms. Identification of factors behind the level and duration of persistence of the SARS-CoV-2 antibodies in the blood is assumed to set the direction for studying humoral immunity mechanisms against COVID-19, optimizing the strategy for vaccine use, antibody-based drugs, and epidemiological control of COVID-19. Objective: This study aimed to study the relationship between clinical and demographic characteristics and the level of IgG antibodies to the RBD of SARS-CoV-2 spike protein after COVID-19 in the long term. Residents of the Altai Region of Western Siberia of Russia, Caucasians, aged from 27 to 93 years (median 53.0 years), who recovered from COVID-19 between May 2020 and February 2021 ( n = 44) took part in this prospective observational study. The titer of IgG antibodies to the RBD of SARS-CoV-2 spike protein was measured repeatedly in the blood at 4–13 months from the beginning of the clinical manifestation of COVID-19 via the method of enzyme-linked immunosorbent assay. The antibody titer positively correlated with age ( p = 0.013) and COVID-19 pneumonia ( p = 0.002) at 20–40 and 20–24 weeks from the onset of COVID-19 symptoms, respectively. Age was positively associated with antibody titer regardless of history of COVID-19 pneumonia (beta regression coefficient p = 0.009). The antibody titer decreased in 15 (34.1%) patients, increased in 10 (22.7%) patients, and did not change in 19 (43.2%) patients from the baseline to 48–49 weeks from the onset of COVID-19 symptoms, with seropositivity persisting in all patients. Age and COVID-19 pneumonia are possibly associated with higher IgG antibodies to the spike protein RBD of SARS-CoV-2 following COVID-19 in the long term. Divergent trends of anti-RBD IgG levels in adults illustrate inter-individual differences at 4–13 months from the onset of COVID-19 symptoms. Identification of factors behind the level and duration of persistence of the SARS-CoV-2 antibodies in the blood is assumed to set the direction for studying humoral immunity mechanisms against COVID-19, optimizing the strategy for vaccine use, antibody-based drugs, and epidemiological control of COVID-19. Objective: This study aimed to study the relationship between clinical and demographic characteristics and the level of IgG antibodies to the RBD of SARS-CoV-2 spike protein after COVID-19 in the long term. Residents of the Altai Region of Western Siberia of Russia, Caucasians, aged from 27 to 93 years (median 53.0 years), who recovered from COVID-19 between May 2020 and February 2021 (n = 44) took part in this prospective observational study. The titer of IgG antibodies to the RBD of SARS-CoV-2 spike protein was measured repeatedly in the blood at 4-13 months from the beginning of the clinical manifestation of COVID-19 via the method of enzyme-linked immunosorbent assay. The antibody titer positively correlated with age (p = 0.013) and COVID-19 pneumonia (p = 0.002) at 20-40 and 20-24 weeks from the onset of COVID-19 symptoms, respectively. Age was positively associated with antibody titer regardless of history of COVID-19 pneumonia (beta regression coefficient p = 0.009). The antibody titer decreased in 15 (34.1%) patients, increased in 10 (22.7%) patients, and did not change in 19 (43.2%) patients from the baseline to 48-49 weeks from the onset of COVID-19 symptoms, with seropositivity persisting in all patients. Age and COVID-19 pneumonia are possibly associated with higher IgG antibodies to the spike protein RBD of SARS-CoV-2 following COVID-19 in the long term. Divergent trends of anti-RBD IgG levels in adults illustrate inter-individual differences at 4-13 months from the onset of COVID-19 symptoms.Identification of factors behind the level and duration of persistence of the SARS-CoV-2 antibodies in the blood is assumed to set the direction for studying humoral immunity mechanisms against COVID-19, optimizing the strategy for vaccine use, antibody-based drugs, and epidemiological control of COVID-19. Objective: This study aimed to study the relationship between clinical and demographic characteristics and the level of IgG antibodies to the RBD of SARS-CoV-2 spike protein after COVID-19 in the long term. Residents of the Altai Region of Western Siberia of Russia, Caucasians, aged from 27 to 93 years (median 53.0 years), who recovered from COVID-19 between May 2020 and February 2021 (n = 44) took part in this prospective observational study. The titer of IgG antibodies to the RBD of SARS-CoV-2 spike protein was measured repeatedly in the blood at 4-13 months from the beginning of the clinical manifestation of COVID-19 via the method of enzyme-linked immunosorbent assay. The antibody titer positively correlated with age (p = 0.013) and COVID-19 pneumonia (p = 0.002) at 20-40 and 20-24 weeks from the onset of COVID-19 symptoms, respectively. Age was positively associated with antibody titer regardless of history of COVID-19 pneumonia (beta regression coefficient p = 0.009). The antibody titer decreased in 15 (34.1%) patients, increased in 10 (22.7%) patients, and did not change in 19 (43.2%) patients from the baseline to 48-49 weeks from the onset of COVID-19 symptoms, with seropositivity persisting in all patients. Age and COVID-19 pneumonia are possibly associated with higher IgG antibodies to the spike protein RBD of SARS-CoV-2 following COVID-19 in the long term. Divergent trends of anti-RBD IgG levels in adults illustrate inter-individual differences at 4-13 months from the onset of COVID-19 symptoms. Identification of factors behind the level and duration of persistence of the SARS-CoV-2 antibodies in the blood is assumed to set the direction for studying humoral immunity mechanisms against COVID-19, optimizing the strategy for vaccine use, antibody-based drugs, and epidemiological control of COVID-19. Objective: This study aimed to study the relationship between clinical and demographic characteristics and the level of IgG antibodies to the RBD of SARS-CoV-2 spike protein after COVID-19 in the long term. Residents of the Altai Region of Western Siberia of Russia, Caucasians, aged from 27 to 93 years (median 53.0 years), who recovered from COVID-19 between May 2020 and February 2021 ( = 44) took part in this prospective observational study. The titer of IgG antibodies to the RBD of SARS-CoV-2 spike protein was measured repeatedly in the blood at 4-13 months from the beginning of the clinical manifestation of COVID-19 via the method of enzyme-linked immunosorbent assay. The antibody titer positively correlated with age ( = 0.013) and COVID-19 pneumonia ( = 0.002) at 20-40 and 20-24 weeks from the onset of COVID-19 symptoms, respectively. Age was positively associated with antibody titer regardless of history of COVID-19 pneumonia (beta regression coefficient = 0.009). The antibody titer decreased in 15 (34.1%) patients, increased in 10 (22.7%) patients, and did not change in 19 (43.2%) patients from the baseline to 48-49 weeks from the onset of COVID-19 symptoms, with seropositivity persisting in all patients. Age and COVID-19 pneumonia are possibly associated with higher IgG antibodies to the spike protein RBD of SARS-CoV-2 following COVID-19 in the long term. Divergent trends of anti-RBD IgG levels in adults illustrate inter-individual differences at 4-13 months from the onset of COVID-19 symptoms. |
Author | Nikulina, Yuliya A. Isaeva, Anastasiya A. Nikonorova, Marina A. Volosnikova, Ekaterina A. Merkuleva, Iuliia A. Shcherbakov, Dmitry N. Nesmeyanova, Valentina S. Belenkaya, Svetlana V. Shanshin, Daniil V. Kolosova, Evgeniia A. Nikitin, Artem O. Elchaninova, Svetlana A. Shaprova, Olga N. |
AuthorAffiliation | 1 State Research Center of Virology and Biotechnology VECTOR, Rospotrebnadzor, 630559 Koltsovo, Russia; ngelya209@gmail.com (O.N.S.); dan6091154224@gmail.com (D.V.S.); nesmeyanova_vs@vector.nsc.ru (V.S.N.); j.a.merkulyeva@gmail.com (I.A.M.); belenkaya.sveta@gmail.com (S.V.B.); anastasya_isaeva_1993@mail.ru (A.A.I.); a.nikitin1@g.nsu.ru (A.O.N.); volosnikova_ea@vector.nsc.ru (E.A.V.); dnshcherbakov@gmail.com (D.N.S.) 4 Department of Biochemistry and Clinical Laboratory Diagnostics, Altai State Medical University, 656038 Barnaul, Russia; saelch@mail.ru 2 Russian-American Anti-Cancer Center, Altai State University, 656049 Barnaul, Russia 3 Department of Infectious Diseases, Altai State Medical University, 656038 Barnaul, Russia; julia_didenko91@mail.ru (Y.A.N.); ma.nikulina@mail.ru (M.A.N.) |
AuthorAffiliation_xml | – name: 3 Department of Infectious Diseases, Altai State Medical University, 656038 Barnaul, Russia; julia_didenko91@mail.ru (Y.A.N.); ma.nikulina@mail.ru (M.A.N.) – name: 1 State Research Center of Virology and Biotechnology VECTOR, Rospotrebnadzor, 630559 Koltsovo, Russia; ngelya209@gmail.com (O.N.S.); dan6091154224@gmail.com (D.V.S.); nesmeyanova_vs@vector.nsc.ru (V.S.N.); j.a.merkulyeva@gmail.com (I.A.M.); belenkaya.sveta@gmail.com (S.V.B.); anastasya_isaeva_1993@mail.ru (A.A.I.); a.nikitin1@g.nsu.ru (A.O.N.); volosnikova_ea@vector.nsc.ru (E.A.V.); dnshcherbakov@gmail.com (D.N.S.) – name: 2 Russian-American Anti-Cancer Center, Altai State University, 656049 Barnaul, Russia – name: 4 Department of Biochemistry and Clinical Laboratory Diagnostics, Altai State Medical University, 656038 Barnaul, Russia; saelch@mail.ru |
Author_xml | – sequence: 1 givenname: Evgeniia A. orcidid: 0000-0002-8967-4719 surname: Kolosova fullname: Kolosova, Evgeniia A. – sequence: 2 givenname: Olga N. surname: Shaprova fullname: Shaprova, Olga N. – sequence: 3 givenname: Daniil V. orcidid: 0000-0001-9985-1582 surname: Shanshin fullname: Shanshin, Daniil V. – sequence: 4 givenname: Valentina S. surname: Nesmeyanova fullname: Nesmeyanova, Valentina S. – sequence: 5 givenname: Iuliia A. orcidid: 0000-0002-6974-0686 surname: Merkuleva fullname: Merkuleva, Iuliia A. – sequence: 6 givenname: Svetlana V. orcidid: 0000-0002-3883-6335 surname: Belenkaya fullname: Belenkaya, Svetlana V. – sequence: 7 givenname: Anastasiya A. surname: Isaeva fullname: Isaeva, Anastasiya A. – sequence: 8 givenname: Artem O. surname: Nikitin fullname: Nikitin, Artem O. – sequence: 9 givenname: Ekaterina A. surname: Volosnikova fullname: Volosnikova, Ekaterina A. – sequence: 10 givenname: Yuliya A. orcidid: 0000-0001-8931-0889 surname: Nikulina fullname: Nikulina, Yuliya A. – sequence: 11 givenname: Marina A. surname: Nikonorova fullname: Nikonorova, Marina A. – sequence: 12 givenname: Dmitry N. orcidid: 0000-0001-8023-4453 surname: Shcherbakov fullname: Shcherbakov, Dmitry N. – sequence: 13 givenname: Svetlana A. surname: Elchaninova fullname: Elchaninova, Svetlana A. |
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Cites_doi | 10.1126/science.abe3255 10.1038/s41423-020-00588-2 10.1038/s41586-021-03696-9 10.1371/journal.pone.0165332 10.1016/S0021-9258(19)52451-6 10.1038/s41467-021-24979-9 10.1016/j.cell.2021.01.007 10.1111/cei.13582 10.3389/fimmu.2021.708523 10.1128/mSphere.00802-20 10.1128/mBio.02940-20 10.1016/j.xcrm.2020.100126 10.1093/infdis/jiab255 10.1038/s41586-020-2852-1 10.1101/2020.08.25.20178806 10.1038/s41586-021-03207-w 10.1126/science.abf4063 10.3390/pathogens10111421 10.1016/j.immuni.2020.07.020 10.1001/jama.2020.16656 10.3346/jkms.2021.36.e54 10.1016/j.cell.2020.02.052 10.1007/s12026-021-09198-0 10.1002/rmv.2195 10.1016/j.cell.2021.02.037 10.1016/j.immuni.2021.01.014 10.1038/s41586-020-2456-9 10.1172/JCI142804 10.1016/j.ejim.2021.05.010 |
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References | Atyeo (ref_27) 2020; 53 Yao (ref_18) 2021; 224 Guthmiller (ref_25) 2021; 12 ref_14 Lotfi (ref_5) 2021; 69 ref_13 Terpos (ref_24) 2021; 89 ref_11 ref_33 Ortega (ref_30) 2021; 12 Gallais (ref_16) 2021; 5 Sette (ref_2) 2021; 184 Wang (ref_22) 2021; 595 Quast (ref_32) 2021; 54 ref_15 Lowry (ref_10) 1951; 193 Barnes (ref_3) 2020; 588 Legros (ref_26) 2021; 18 Zhou (ref_31) 2021; 184 Robbiani (ref_28) 2020; 584 Schoof (ref_12) 2020; 370 Dan (ref_23) 2021; 371 Stephens (ref_1) 2020; 324 Gaebler (ref_19) 2021; 591 Byrnes (ref_6) 2020; 5 Gasser (ref_21) 2020; 1 Yoo (ref_17) 2021; 36 Xiang (ref_20) 2021; 12 Hoffmann (ref_29) 2020; 181 Jordan (ref_4) 2021; 204 ref_8 Secchi (ref_7) 2020; 130 Liu (ref_9) 2021; 31 |
References_xml | – volume: 370 start-page: 1473 year: 2020 ident: ref_12 article-title: An ultrapotent synthetic nanobody neutralizes SARS-CoV-2 by stabilizing inactive Spike publication-title: Science doi: 10.1126/science.abe3255 – volume: 18 start-page: 318 year: 2021 ident: ref_26 article-title: A longitudinal study of SARS-CoV-2-infected patients reveals a high correlation between neutralizing antibodies and COVID-19 severity publication-title: Cell. Mol. Immunol. doi: 10.1038/s41423-020-00588-2 – volume: 595 start-page: 426 year: 2021 ident: ref_22 article-title: Naturally enhanced neutralizing breadth against SARS-CoV-2 one year after infection publication-title: Nature doi: 10.1038/s41586-021-03696-9 – ident: ref_11 doi: 10.1371/journal.pone.0165332 – volume: 193 start-page: 265 year: 1951 ident: ref_10 article-title: Protein measurement with the Folin phenol reagent publication-title: J. Biol. Chem. doi: 10.1016/S0021-9258(19)52451-6 – volume: 12 start-page: 4740 year: 2021 ident: ref_30 article-title: Seven-month kinetics of SARS-CoV-2 antibodies and role of pre-existing antibodies to human coronaviruses publication-title: Nat. Commun. doi: 10.1038/s41467-021-24979-9 – volume: 184 start-page: 861 year: 2021 ident: ref_2 article-title: Adaptive immunity to SARS-CoV-2 and COVID-19 publication-title: Cell doi: 10.1016/j.cell.2021.01.007 – ident: ref_14 – volume: 5 start-page: 21256823 year: 2021 ident: ref_16 article-title: Anti-SARS-CoV-2 Antibodies persist for up to 13 months and reduce risk of reinfection publication-title: medRxiv – volume: 204 start-page: 310 year: 2021 ident: ref_4 article-title: Innate and adaptive immune responses to SARS-CoV-2 in humans: Relevance to acquired immunity and vaccine responses publication-title: Clin. Exp. Immunol. doi: 10.1111/cei.13582 – volume: 12 start-page: 708523 year: 2021 ident: ref_20 article-title: Declining levels of neutralizing antibodies against SARS-CoV-2 in convalescent COVID-19 patients one year post symptom onset publication-title: Front. Immunol. doi: 10.3389/fimmu.2021.708523 – volume: 5 start-page: e00802-20 year: 2020 ident: ref_6 article-title: Competitive SARS-CoV-2 serology reveals most antibodies targeting the spike receptor-binding domain compete for ACE2 binding publication-title: mSphere doi: 10.1128/mSphere.00802-20 – volume: 12 start-page: e02940-20 year: 2021 ident: ref_25 article-title: SARS-CoV-2 Infection severity is linked to superior humoral immunity against the spike publication-title: mBio doi: 10.1128/mBio.02940-20 – volume: 1 start-page: 100126 year: 2020 ident: ref_21 article-title: Cross-sectional evaluation of humoral responses against SARS-CoV-2 spike publication-title: Cell. Rep. Med. doi: 10.1016/j.xcrm.2020.100126 – volume: 224 start-page: 586 year: 2021 ident: ref_18 article-title: Persistence of antibody and cellular immune responses in COVID-19 patients over nine months after infection publication-title: J. Infect. Dis. doi: 10.1093/infdis/jiab255 – volume: 588 start-page: 682 year: 2020 ident: ref_3 article-title: SARS-CoV-2 neutralizing antibody structures inform therapeutic strategies publication-title: Nature doi: 10.1038/s41586-020-2852-1 – ident: ref_8 doi: 10.1101/2020.08.25.20178806 – volume: 591 start-page: 639 year: 2021 ident: ref_19 article-title: Evolution of antibody immunity to SARS-CoV-2 publication-title: Nature doi: 10.1038/s41586-021-03207-w – volume: 371 start-page: eabf4063 year: 2021 ident: ref_23 article-title: Immunological memory to SARS-CoV-2 assessed for up to 8 months after infection publication-title: Science doi: 10.1126/science.abf4063 – ident: ref_13 doi: 10.3390/pathogens10111421 – volume: 53 start-page: 524 year: 2020 ident: ref_27 article-title: Distinct early serological signatures track with SARS-CoV-2 survival publication-title: Immunity doi: 10.1016/j.immuni.2020.07.020 – ident: ref_33 – volume: 324 start-page: 1279 year: 2020 ident: ref_1 article-title: COVID-19 and the Path to Immunity publication-title: JAMA doi: 10.1001/jama.2020.16656 – volume: 36 start-page: e54 year: 2021 ident: ref_17 article-title: What we do know and do not yet know about COVID-19 vaccines as of the beginning of the year 2021 publication-title: J. Korean. Med. Sci. doi: 10.3346/jkms.2021.36.e54 – volume: 181 start-page: 271 year: 2020 ident: ref_29 article-title: SARS-CoV-2 Cell Entry Depends on ACE2 and TMPRSS2 and Is Blocked by a Clinically Proven Protease Inhibitor publication-title: Cell doi: 10.1016/j.cell.2020.02.052 – volume: 69 start-page: 213 year: 2021 ident: ref_5 article-title: A review on the immune responses against novel emerging coronavirus (SARS-CoV-2) publication-title: Immunol. Res. doi: 10.1007/s12026-021-09198-0 – volume: 31 start-page: e2195 year: 2021 ident: ref_9 article-title: A systematic meta-analysis of immune signatures in patients with COVID-19 publication-title: Rev. Med. Virol. doi: 10.1002/rmv.2195 – ident: ref_15 – volume: 184 start-page: 2348 year: 2021 ident: ref_31 article-title: Evidence of escape of SARS-CoV-2 variant B.1.351 from natural and vaccine-induced sera publication-title: Cell doi: 10.1016/j.cell.2021.02.037 – volume: 54 start-page: 205 year: 2021 ident: ref_32 article-title: B cell memory: Understanding COVID-19 publication-title: Immunity doi: 10.1016/j.immuni.2021.01.014 – volume: 584 start-page: 437 year: 2020 ident: ref_28 article-title: Convergent antibody responses to SARS-CoV-2 in convalescent individuals publication-title: Nature doi: 10.1038/s41586-020-2456-9 – volume: 130 start-page: 6366 year: 2020 ident: ref_7 article-title: COVID-19 survival associates with the immunoglobulin response to the SARS-CoV-2 spike receptor binding domain publication-title: J. Clin. Investig. doi: 10.1172/JCI142804 – volume: 89 start-page: 87 year: 2021 ident: ref_24 article-title: SARS-CoV-2 antibody kinetics eight months from COVID-19 onset: Persistence of spike antibodies but loss of neutralizing antibodies in 24% of convalescent plasma donors publication-title: Eur. J. Intern. Med. doi: 10.1016/j.ejim.2021.05.010 |
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Title | Antibodies to the Spike Protein Receptor-Binding Domain of SARS-CoV-2 at 4–13 Months after COVID-19 |
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