| Literature DB >> 33338412 |
Min-Seok Rha1, Hye Won Jeong2, Jae-Hoon Ko3, Seong Jin Choi1, In-Ho Seo1, Jeong Seok Lee4, Moa Sa5, A Reum Kim1, Eun-Jeong Joo6, Jin Young Ahn7, Jung Ho Kim7, Kyoung-Ho Song8, Eu Suk Kim8, Dong Hyun Oh9, Mi Young Ahn9, Hee Kyoung Choi10, Ji Hoon Jeon10, Jae-Phil Choi9, Hong Bin Kim8, Young Keun Kim11, Su-Hyung Park5, Won Suk Choi12, Jun Yong Choi13, Kyong Ran Peck14, Eui-Cheol Shin15.
Abstract
Memory T cell responses have been demonstrated in COVID-19 convalescents, but ex vivo phenotypes of SARS-CoV-2-specific T cells have been unclear. We detected SARS-CoV-2-specific CD8+ T cells by MHC class I multimer staining and examined their phenotypes and functions in acute and convalescent COVID-19. Multimer+ cells exhibited early differentiated effector-memory phenotypes in the early convalescent phase. The frequency of stem-like memory cells was increased among multimer+ cells in the late convalescent phase. Cytokine secretion assays combined with MHC class I multimer staining revealed that the proportion of interferon-γ (IFN-γ)-producing cells was significantly lower among SARS-CoV-2-specific CD8+ T cells than those specific to influenza A virus. Importantly, the proportion of IFN-γ-producing cells was higher in PD-1+ cells than PD-1- cells among multimer+ cells, indicating that PD-1-expressing, SARS-CoV-2-specific CD8+ T cells are not exhausted, but functional. Our current findings provide information for understanding of SARS-CoV-2-specific CD8+ T cells elicited by infection or vaccination.Entities:
Keywords: CD8(+) T cell; COVID-19; IFN-γ; MHC class I multimer; Memory T cell; PD-1; SARS-CoV-2
Year: 2020 PMID: 33338412 DOI: 10.1016/j.immuni.2020.12.002
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745