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 inJournal of clinical medicine Vol. 11; no. 14; p. 4053
Main Authors Kolosova, Evgeniia A., Shaprova, Olga N., Shanshin, Daniil V., Nesmeyanova, Valentina S., Merkuleva, Iuliia A., Belenkaya, Svetlana V., Isaeva, Anastasiya A., Nikitin, Artem O., Volosnikova, Ekaterina A., Nikulina, Yuliya A., Nikonorova, Marina A., Shcherbakov, Dmitry N., Elchaninova, Svetlana A.
Format Journal Article
LanguageEnglish
Published Switzerland MDPI AG 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.
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.)
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CitedBy_id crossref_primary_10_3390_ijms232213681
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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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Issue 14
Keywords COVID-19
SARS-CoV-2
pneumonia
receptor-binding domain
spike protein
antibodies
age
Language English
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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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SubjectTerms Antibodies
Chromatography
Clinical medicine
Cloning
Coronaviruses
COVID-19
Enzymes
Infections
Medical research
Plasmids
Proteins
Severe acute respiratory syndrome coronavirus 2
Sodium
Vectors (Biology)
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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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