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Microbiol Spectr . High-Resolution Linear Epitope Mapping of the Receptor Binding Domain of SARS-CoV-2 Spike Protein in COVID-19 mRNA Vaccine Recip

tetano

Editor, Senior Moderator
Microbiol Spectr


. 2021 Nov 10;e0096521.
doi: 10.1128/Spectrum.00965-21. Online ahead of print.
High-Resolution Linear Epitope Mapping of the Receptor Binding Domain of SARS-CoV-2 Spike Protein in COVID-19 mRNA Vaccine Recipients


Yuko Nitahara[SUP] 1 [/SUP], Yu Nakagama[SUP] 1 [/SUP], Natsuko Kaku[SUP] 1 [/SUP], Katherine Candray[SUP] 1 [/SUP], Yu Michimuko[SUP] 1 [/SUP], Evariste Tshibangu-Kabamba[SUP] 1 [/SUP], Akira Kaneko[SUP] 1 [/SUP], Hiromasa Yamamoto[SUP] 2 [/SUP], Yasumitsu Mizobata[SUP] 2 [/SUP], Hiroshi Kakeya[SUP] 3 [/SUP], Mayo Yasugi[SUP] 4 5 6 [/SUP], Yasutoshi Kido[SUP] 1 [/SUP]



Affiliations

Abstract

The prompt rollout of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) mRNA vaccine is facilitating population immunity, which is becoming more dominant than natural infection-mediated immunity. In the midst of coronavirus disease 2019 (COVID-19) vaccine deployment, understanding the epitope profiles of vaccine-elicited antibodies will be the first step in assessing the functionality of vaccine-induced immunity. In this study, the high-resolution linear epitope profiles of Pfizer-BioNTech COVID-19 mRNA vaccine recipients and COVID-19 patients were delineated by using microarrays mapped with overlapping peptides of the receptor binding domain (RBD) of the SARS-CoV-2 spike protein. The vaccine-induced antibodies targeting the RBD had a broader distribution across the RBD than that induced by the natural infection. Half-maximal neutralization titers were measured in vitro by live virus neutralization assays. As a result, relatively lower neutralizability was observed in vaccine recipient sera, when normalized to a total anti-RBD IgG titer. However, mutation panel assays targeting the SARS-CoV-2 variants of concern have shown that the vaccine-induced epitope variety, rich in breadth, may grant resistance against future viral evolutionary escapes, serving as an advantage of vaccine-induced immunity. IMPORTANCE Establishing vaccine-based population immunity has been the key factor in attaining herd protection. Thanks to expedited worldwide research efforts, the potency of mRNA vaccines against the coronavirus disease 2019 (COVID-19) is now incontestable. The next debate is regarding the coverage of SARS-CoV-2 variants. In the midst of vaccine deployment, it is of importance to describe the similarities and differences between the immune responses of COVID-19 vaccine recipients and naturally infected individuals. In this study, we demonstrated that the antibody profiles of vaccine recipients are richer in variety, targeting a key protein of the invading virus, than those of naturally infected individuals. Vaccine-elicited antibodies included more nonneutralizing antibodies than infection-elicited antibodies, and their breadth in antibody variations suggested possible resilience against future SARS-CoV-2 variants. The antibody profile achieved by vaccinations in naive individuals provides important insight into the first step toward vaccine-based population immunity.

Keywords: COVID-19; RBD; SARS-CoV-2; immunoserology; neutralizing antibodies; serology; spike; spike protein.
 
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