Divergent Antibody Repertoires Found for Omicron versus Wuhan SARS-CoV-2 Strains Using Ig-MS.
Autor: | Forte E; Proteomics Center of Excellence, Evanston, Illinois60208, United States.; Department of Surgery, Comprehensive Transplant Center, Feinberg School of Medicine, Northwestern University, Chicago, Illinois60611, United States., Des Soye BJ; Proteomics Center of Excellence, Evanston, Illinois60208, United States., Melani RD; Proteomics Center of Excellence, Evanston, Illinois60208, United States.; Department of Molecular Biosciences, Chemistry, Northwestern University, Evanston, Illinois60208, United States., Hollas MAR; Proteomics Center of Excellence, Evanston, Illinois60208, United States., Kafader JO; Proteomics Center of Excellence, Evanston, Illinois60208, United States., Sha BE; Division of Infectious Diseases, Rush University Medical Center, Chicago, Illinois60612, United States., Schneider JR; Department of Microbial Pathogens and Immunity, Rush University Medical Center, Chicago, Illinois60612, United States., Kelleher NL; Proteomics Center of Excellence, Evanston, Illinois60208, United States.; Department of Surgery, Comprehensive Transplant Center, Feinberg School of Medicine, Northwestern University, Chicago, Illinois60611, United States.; Department of Biochemistry and Molecular Genetics, Northwestern University Feinberg School of Medicine, Chicago, Illinois60611, United States. |
---|---|
Jazyk: | angličtina |
Zdroj: | Journal of proteome research [J Proteome Res] 2022 Dec 02; Vol. 21 (12), pp. 2987-2997. Date of Electronic Publication: 2022 Nov 07. |
DOI: | 10.1021/acs.jproteome.2c00514 |
Abstrakt: | SARS-CoV-2 Omicron (B.1.1.529) and its subvariants are currently the most common variants of concern worldwide, featuring numerous mutations in the spike protein and elsewhere that collectively make Omicron variants more transmissible and more resistant to antibody-mediated neutralization provided by vaccination, previous infections, and monoclonal antibody therapies than their predecessors. We recently reported the creation and characterization of Ig-MS, a new mass spectrometry-based serology platform that can define the repertoire of antibodies against an antigen of interest at single proteoform resolution. Here, we applied Ig-MS to investigate the evolution of plasma antibody repertoires against the receptor-binding domain (RBD) of SARS-CoV-2 in response to the booster shot and natural viral infection. We also assessed the capacity for antibody repertoires generated in response to vaccination and/or infection with the Omicron variant to bind to both Wuhan- and Omicron-RBDs. Our results show that (1) the booster increases antibody titers against both Wuhan- and Omicron- RBDs and elicits an Omicron-specific response and (2) vaccination and infection act synergistically in generating anti-RBD antibody repertoires able to bind both Wuhan- and Omicron-RBDs with variant-specific antibodies. |
Databáze: | MEDLINE |
Externí odkaz: |