| Literature DB >> 33777028 |
Asgar Ansari1, Rakesh Arya2, Shilpa Sachan1, Someshwar Nath Jha1, Anurag Kalia1, Anupam Lall3, Alessandro Sette4,5, Alba Grifoni4, Daniela Weiskopf4, Poonam Coshic3, Ashok Sharma2, Nimesh Gupta1.
Abstract
Understanding the causes of the diverse outcome of COVID-19 pandemic in different geographical locations is important for the worldwide vaccine implementation and pandemic control responses. We analyzed 42 unexposed healthy donors and 28 mild COVID-19 subjects up to 5 months from the recovery for SARS-CoV-2 specific immunological memory. Using HLA class II predicted peptide megapools, we identified SARS-CoV-2 cross-reactive CD4+ T cells in around 66% of the unexposed individuals. Moreover, we found detectable immune memory in mild COVID-19 patients several months after recovery in the crucial arms of protective adaptive immunity; CD4+ T cells and B cells, with a minimal contribution from CD8+ T cells. Interestingly, the persistent immune memory in COVID-19 patients is predominantly targeted towards the Spike glycoprotein of the SARS-CoV-2. This study provides the evidence of both high magnitude pre-existing and persistent immune memory in Indian population. By providing the knowledge on cellular immune responses to SARS-CoV-2, our work has implication for the development and implementation of vaccines against COVID-19.Entities:
Keywords: B cells; CD4+ T cells; human coronavirus; neutralizing antibody; pre-existing immunity
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Year: 2021 PMID: 33777028 PMCID: PMC7991090 DOI: 10.3389/fimmu.2021.636768
Source DB: PubMed Journal: Front Immunol ISSN: 1664-3224 Impact factor: 7.561