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

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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.

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.

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관련 논문AI추천

SARS-CoV-2-Specific T Cell Responses in Patients with COVID-19 and Unexposed Individuals김아름, 나민석, 신의철대한면역학회 · Immune Network2021 · 제21권 제1호SARS-CoV-2 mRNA Vaccine Elicits Sustained T Cell Responses Against the Omicron Variant in Adolescents신의철, 윤기욱, 최은화, Ahn Bin, Choe Young June, Cho Hye-Kyung, Choi Eun Bee, Choi Sujin, Choi Sung Hwan, Han Mi Seon, Hyeon Seokhwan, Kim Byung-chul, Kim Kwangwook, Kim Sang-Hoon, Kim Ye Kyung, Kim Yun-Kyung, Lee Hyunju, Lee Yoo-kyoung, Lim Heeji, Lim Hye Jung, Song Seung Ha, Yoon Yoonsun대한면역학회 · Immune Network2023 · 제23권 제4호Pre-existing Immunity to Endemic Human Coronaviruses Does Not Affect the Immune Response to SARS-CoV-2 Spike in a Murine Vaccination Model김두진, Jeong Ahn Young, Lee Moo-Seung, Lee Pureum대한면역학회 · Immune Network2023 · 제23권 제2호Evaluation of Cellular Responses to ChAdOx1-nCoV-19 and BNT162b2 Vaccinations남민정, 문희원, Hur Mina, Kim Hae-Rim, Kim Hanah, Lee Tae Hwan, Seo Jong Do, Yun Yeo-Min대한진단검사의학회 · Annals of Laboratory Medicine2023 · 제43권 제3호Omicron Subvariants, Including BA.4 and BA.5, Substantially Preserve T Cell Epitopes of Ancestral SARS-CoV-2박계명, 신의철, 최성진대한면역학회 · Immune Network2022 · 제22권 제4호Comparison of Four T-cell Assays and Two Binding Antibody Assays in SARS-CoV-2 Vaccinees With or Without Omicron Breakthrough Infection신수, 남민정, 노은연, 송은영, Oh Inseong, Seo Yeon Ju대한진단검사의학회 · Annals of Laboratory Medicine2023 · 제43권 제6호

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