| Literature DB >> 33674317 |
Supriya Ravichandran1, Youri Lee1, Gabrielle Grubbs1, Elizabeth M Coyle1, Laura Klenow1, Osamu Akasaka2, Michiko Koga3, Eisuke Adachi3, Makoto Saito3, Ichiro Nakachi4, Takayuki Ogura5, Rie Baba4, Mutsumi Ito6, Maki Kiso6, Atsuhiro Yasuhara6, Shinya Yamada6, Yuko Sakai-Tagawa6, Kiyoko Iwatsuki-Horimoto6, Masaki Imai6, Seiya Yamayoshi6, Hiroshi Yotsuyanagi3, Yoshihiro Kawaoka6,7, Surender Khurana8.
Abstract
Limited knowledge exists on immune markers associated with disease severity or recovery in patients with coronavirus disease 2019 (COVID-19). Here, we elucidated longitudinal evolution of SARS-CoV-2 antibody repertoire in patients with acute COVID-19. Differential kinetics was observed for immunoglobulin M (IgM)/IgG/IgA epitope diversity, antibody binding, and affinity maturation in "severe" versus "mild" COVID-19 patients. IgG profile demonstrated immunodominant antigenic sequences encompassing fusion peptide and receptor binding domain (RBD) in patients with mild COVID-19 who recovered early compared with "fatal" COVID-19 patients. In patients with severe COVID-19, high-titer IgA were observed, primarily against RBD, especially in patients who succumbed to SARS-CoV-2 infection. The patients with mild COVID-19 showed marked increase in antibody affinity maturation to prefusion SARS-CoV-2 spike that associated with faster recovery from COVID-19. This study revealed antibody markers associated with disease severity and resolution of clinical disease that could inform development and evaluation of effective immune-based countermeasures against COVID-19.Entities:
Year: 2021 PMID: 33674317 DOI: 10.1126/sciadv.abf2467
Source DB: PubMed Journal: Sci Adv ISSN: 2375-2548 Impact factor: 14.136