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Patients With Mild COVID-19 Exhibit Low Functional Avidity of SARS-CoV-2 Membrane Protein-Reactive CD4+T Cells

Authors
 A-Reum Kim  ;  June-Young Koh  ;  Min-Seok Rha  ;  Jae Hyung Jung  ;  Jae-Hoon Ko  ;  Hee Kyoung Choi  ;  Ji Hoon Jeon  ;  Hyeri Seok  ;  Dae Won Park  ;  Kyong Ran Peck  ;  Jun Yong Choi  ;  Su-Hyung Park  ;  Won Suk Choi  ;  Hye Won Jeong  ;  Eui-Cheol Shin 
Citation
 IMMUNE NETWORK, Vol.25(2) : e4, 2025-04 
Journal Title
IMMUNE NETWORK
ISSN
 1598-2629 
Issue Date
2025-04
Keywords
CD4-positive-T-lymphocytes ; COVID-19 ; Cross-reactivity ; Functional avidity ; SARS-CoV-2
Abstract
Herein, we found that severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)-unexposed individuals exhibited an increased frequency of CD4+ T cells against SARS-CoV-2 membrane (M) protein, suggesting that SARS-CoV-2 M-reactive cells may be primed by previous infection with common cold coronaviruses (CCCoVs). We confirmed that CCCoV M-reactive CD4+ T cells cross-recognize SARS-CoV-2 M in unexposed individuals. Among coronavirus disease 2019 (COVID-19) convalescents and unexposed individuals, SARS-CoV-2 M-reactive CD4+ T cells exhibited significantly lower functional avidity than CD4+ T cells reactive to other viruses. Importantly, convalescents from mild COVID-19 had SARS-CoV-2 M-reactive CD4+ T cells with significantly lower functional avidity than convalescents from severe COVID-19. The current data suggest that pre-existing CCCoV M-specific memory CD4+ T cells may contribute to controlling SARS-CoV-2 infection by cross-reactivity, leading to mild disease but leaving memory cells with low functional avidity to SARS-CoV-2 M due to incomplete homology. These data provide indirect evidence that pre-existing cross-reactive CD4+ T cells contribute to protection from severe COVID-19.
Files in This Item:
T202503703.pdf Download
DOI
10.4110/in.2025.25.e4
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
Yonsei Authors
Choi, Jun Yong(최준용) ORCID logo https://orcid.org/0000-0002-2775-3315
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/206231
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