Frontiers in Immunology (Sep 2022)

Mapping monoclonal anti-SARS-CoV-2 antibody repertoires against diverse coronavirus antigens

  • Matheus Oliveira de Souza,
  • Matheus Oliveira de Souza,
  • Bharat Madan,
  • Bharat Madan,
  • I-Ting Teng,
  • Aric Huang,
  • Lihong Liu,
  • Ahmed S. Fahad,
  • Sheila N. Lopez Acevedo,
  • Xiaoli Pan,
  • Mallika Sastry,
  • Matias Gutierrez-Gonzalez,
  • Michael T. Yin,
  • Tongqing Zhou,
  • David D. Ho,
  • Peter D. Kwong,
  • Peter D. Kwong,
  • Brandon J. DeKosky,
  • Brandon J. DeKosky,
  • Brandon J. DeKosky,
  • Brandon J. DeKosky

DOI
https://doi.org/10.3389/fimmu.2022.977064
Journal volume & issue
Vol. 13

Abstract

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Variants of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) have emerged continuously, challenging the effectiveness of vaccines, diagnostics, and treatments. Moreover, the possibility of the appearance of a new betacoronavirus with high transmissibility and high fatality is reason for concern. In this study, we used a natively paired yeast display technology, combined with next-generation sequencing (NGS) and massive bioinformatic analysis to perform a comprehensive study of subdomain specificity of natural human antibodies from two convalescent donors. Using this screening technology, we mapped the cross-reactive responses of antibodies generated by the two donors against SARS-CoV-2 variants and other betacoronaviruses. We tested the neutralization potency of a set of the cross-reactive antibodies generated in this study and observed that most of the antibodies produced by these patients were non-neutralizing. We performed a comparison of the specific and non-specific antibodies by somatic hypermutation in a repertoire-scale for the two individuals and observed that the degree of somatic hypermutation was unique for each patient. The data from this study provide functional insights into cross-reactive antibodies that can assist in the development of strategies against emerging SARS-CoV-2 variants and divergent betacoronaviruses.

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