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Landscape of Infection Enhancing Antibodies in COVID-19 and Healthy Donors

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Specialty Biotechnology
Date 2022 Nov 9
PMID 36348766
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Abstract

To assess the frequency of SARS-CoV-2 infection in the general population, we searched over 64 million heavy chain antibody sequences from healthy unvaccinated, healthy BNT162b2 vaccinated and COVID-19 patient repertoires for sequences similar to 11 previously reported enhancing antibodies. Although the distribution of sequence identities was similar in all three groups of repertoires, the COVID-19 and healthy vaccinated hits were significantly more clonally expanded than healthy unvaccinated hits. Furthermore, among the tested hits, 17 out of 94 from COVID-19 and 9 out of 59 from healthy vaccinated, compared with only 2 out of 96 from healthy unvaccinated, bound to the enhancing epitope. A total of 9 of the 28 epitope-binding antibodies enhanced ACE2 receptor binding to the spike protein. Together, this study revealed that infection enhancing-like antibodies are far more frequent in COVID-19 patients or healthy vaccinated donors than in healthy unvaccinated donors, but a reservoir of potential enhancing antibodies exists in healthy donors that could potentially mature to actual enhancing antibodies upon infection.

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References
1.
Zhu J, Wu X, Zhang B, McKee K, ODell S, Soto C . De novo identification of VRC01 class HIV-1-neutralizing antibodies by next-generation sequencing of B-cell transcripts. Proc Natl Acad Sci U S A. 2013; 110(43):E4088-97. PMC: 3808619. DOI: 10.1073/pnas.1306262110. View

2.
Steinegger M, Soding J . MMseqs2 enables sensitive protein sequence searching for the analysis of massive data sets. Nat Biotechnol. 2017; 35(11):1026-1028. DOI: 10.1038/nbt.3988. View

3.
Zhou Y, Zhang J, Wang D, Wang D, Guan W, Qin J . Profiling of the immune repertoire in COVID-19 patients with mild, severe, convalescent, or retesting-positive status. J Autoimmun. 2021; 118:102596. PMC: 7837046. DOI: 10.1016/j.jaut.2021.102596. View

4.
Woodruff M, Ramonell R, Nguyen D, Cashman K, Singh Saini A, Haddad N . Extrafollicular B cell responses correlate with neutralizing antibodies and morbidity in COVID-19. Nat Immunol. 2020; 21(12):1506-1516. PMC: 7739702. DOI: 10.1038/s41590-020-00814-z. View

5.
Victora G, Nussenzweig M . Germinal centers. Annu Rev Immunol. 2012; 30:429-57. DOI: 10.1146/annurev-immunol-020711-075032. View