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Immunity ; 53(6): 1258-1271.e5, 2020 12 15.
Artículo en Inglés | MEDLINE | ID: covidwho-988080

RESUMEN

CD4+ T cells reactive against SARS-CoV-2 can be found in unexposed individuals, and these are suggested to arise in response to common cold coronavirus (CCCoV) infection. Here, we utilized SARS-CoV-2-reactive CD4+ T cell enrichment to examine the antigen avidity and clonality of these cells, as well as the relative contribution of CCCoV cross-reactivity. SARS-CoV-2-reactive CD4+ memory T cells were present in virtually all unexposed individuals examined, displaying low functional avidity and multiple, highly variable cross-reactivities that were not restricted to CCCoVs. SARS-CoV-2-reactive CD4+ T cells from COVID-19 patients lacked cross-reactivity to CCCoVs, irrespective of strong memory T cell responses against CCCoV in all donors analyzed. In severe but not mild COVID-19, SARS-CoV-2-specific T cells displayed low functional avidity and clonality, despite increased frequencies. Our findings identify low-avidity CD4+ T cell responses as a hallmark of severe COVID-19 and argue against a protective role for CCCoV-reactive T cells in SARS-CoV-2 infection.


Asunto(s)
Linfocitos T CD4-Positivos/inmunología , COVID-19/inmunología , Receptores de Antígenos de Linfocitos T/metabolismo , Rhinovirus/inmunología , SARS-CoV-2/inmunología , Antígenos Virales/inmunología , Células Cultivadas , Reacciones Cruzadas , Progresión de la Enfermedad , Exposición a Riesgos Ambientales , Humanos , Memoria Inmunológica , Activación de Linfocitos , Unión Proteica , Índice de Severidad de la Enfermedad , Especificidad del Receptor de Antígeno de Linfocitos T
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