Epitope Coverage of Anti-SARS-CoV-2 Nucleocapsid IgA and IgG Antibodies Correlates with Protection against Re-Infection by New Variants in Subsequent Waves of the COVID-19 Pandemic

dc.contributor.authorMullins, Michelle O.
dc.contributor.authorSmith, Muneerah
dc.contributor.authorMaboreke, Hazel
dc.contributor.authorNel, Andrew J. M.
dc.contributor.authorNtusi, Ntobeko A. B.
dc.contributor.authorBurgers, Wendy A.
dc.contributor.authorBlackburn, Jonathan M.
dc.date.accessioned2024-04-29T10:31:18Z
dc.date.available2024-04-29T10:31:18Z
dc.date.issued2023-02-20
dc.date.updated2023-02-24T14:09:33Z
dc.description.abstractThe COVID-19 pandemic continues to affect individuals across the globe, with some individuals experiencing more severe disease than others. The relatively high frequency of re-infections and breakthrough infections observed with SARS-CoV-2 highlights the importance of extending our understanding of immunity to COVID-19. Here, we aim to shed light on the importance of antibody titres and epitope utilization in protection from re-infection. Health care workers are highly exposed to SARS-CoV-2 and are therefore also more likely to become re-infected. We utilized quantitative, multi-antigen, multi-epitope SARS-CoV-2 protein microarrays to measure IgG and IgA titres against various domains of the nucleocapsid and spike proteins. Potential re-infections in a large, diverse health care worker cohort (N = 300) during the second wave of the pandemic were identified by assessing the IgG anti-N titres before and after the second wave. We assessed epitope coverage and antibody titres between the &lsquo;single infection&rsquo; and &lsquo;re-infection&rsquo; groups. Clear differences were observed in the breadth of the anti-N response before the second wave, with the epitope coverage for both IgG (<i>p</i> = 0.019) and IgA (<i>p</i> = 0.015) being significantly increased in those who did not become re-infected compared to those who did. Additionally, the IgG anti-N (<i>p</i> = 0.004) and anti-S titres (<i>p</i> = 0.018) were significantly higher in those not re-infected. These results highlight the importance of the breadth of elicited antibody epitope coverage following natural infection in protection from re-infection and disease in the COVID-19 pandemic.
dc.identifierdoi: 10.3390/v15020584
dc.identifier.apacitationMullins, Michelle O., Smith, M., Maboreke, H., Nel, Andrew J. M., Ntusi, Ntobeko A. B., Burgers, Wendy A., & Blackburn, Jonathan M. (2023). Epitope Coverage of Anti-SARS-CoV-2 Nucleocapsid IgA and IgG Antibodies Correlates with Protection against Re-Infection by New Variants in Subsequent Waves of the COVID-19 Pandemic. http://hdl.handle.net/11427/39490en_ZA
dc.identifier.chicagocitationMullins, Michelle O., Muneerah Smith, Hazel Maboreke, Andrew J. M. Nel, Ntobeko A. B. Ntusi, Wendy A. Burgers, and Jonathan M. Blackburn "Epitope Coverage of Anti-SARS-CoV-2 Nucleocapsid IgA and IgG Antibodies Correlates with Protection against Re-Infection by New Variants in Subsequent Waves of the COVID-19 Pandemic." (2023) http://hdl.handle.net/11427/39490en_ZA
dc.identifier.citationViruses 15 (2): 584 (2023)
dc.identifier.ris TY - Journal Article AU - Mullins, Michelle O. AU - Smith, Muneerah AU - Maboreke, Hazel AU - Nel, Andrew J. M. AU - Ntusi, Ntobeko A. B. AU - Burgers, Wendy A. AU - Blackburn, Jonathan M. AB - The COVID-19 pandemic continues to affect individuals across the globe, with some individuals experiencing more severe disease than others. The relatively high frequency of re-infections and breakthrough infections observed with SARS-CoV-2 highlights the importance of extending our understanding of immunity to COVID-19. Here, we aim to shed light on the importance of antibody titres and epitope utilization in protection from re-infection. Health care workers are highly exposed to SARS-CoV-2 and are therefore also more likely to become re-infected. We utilized quantitative, multi-antigen, multi-epitope SARS-CoV-2 protein microarrays to measure IgG and IgA titres against various domains of the nucleocapsid and spike proteins. Potential re-infections in a large, diverse health care worker cohort (N = 300) during the second wave of the pandemic were identified by assessing the IgG anti-N titres before and after the second wave. We assessed epitope coverage and antibody titres between the &lsquo;single infection&rsquo; and &lsquo;re-infection&rsquo; groups. Clear differences were observed in the breadth of the anti-N response before the second wave, with the epitope coverage for both IgG (<i>p</i> = 0.019) and IgA (<i>p</i> = 0.015) being significantly increased in those who did not become re-infected compared to those who did. Additionally, the IgG anti-N (<i>p</i> = 0.004) and anti-S titres (<i>p</i> = 0.018) were significantly higher in those not re-infected. These results highlight the importance of the breadth of elicited antibody epitope coverage following natural infection in protection from re-infection and disease in the COVID-19 pandemic. DA - 2023-02-20 DB - OpenUCT DP - University of Cape Town LK - https://open.uct.ac.za PY - 2023 T1 - Epitope Coverage of Anti-SARS-CoV-2 Nucleocapsid IgA and IgG Antibodies Correlates with Protection against Re-Infection by New Variants in Subsequent Waves of the COVID-19 Pandemic TI - Epitope Coverage of Anti-SARS-CoV-2 Nucleocapsid IgA and IgG Antibodies Correlates with Protection against Re-Infection by New Variants in Subsequent Waves of the COVID-19 Pandemic UR - http://hdl.handle.net/11427/39490 ER - en_ZA
dc.identifier.urihttp://hdl.handle.net/11427/39490
dc.identifier.vancouvercitationMullins Michelle O, Smith M, Maboreke H, Nel Andrew J M, Ntusi Ntobeko A B, Burgers Wendy A, et al. Epitope Coverage of Anti-SARS-CoV-2 Nucleocapsid IgA and IgG Antibodies Correlates with Protection against Re-Infection by New Variants in Subsequent Waves of the COVID-19 Pandemic. 2023; http://hdl.handle.net/11427/39490.en_ZA
dc.titleEpitope Coverage of Anti-SARS-CoV-2 Nucleocapsid IgA and IgG Antibodies Correlates with Protection against Re-Infection by New Variants in Subsequent Waves of the COVID-19 Pandemic
dc.typeJournal Article
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