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Impaired Cytotoxic CD8(+) T Cell Response in Elderly COVID-19 Patients

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection induces a T cell response that most likely contributes to virus control in COVID-19 patients but may also induce immunopathology. Until now, the cytotoxic T cell response has not been very well characterized in COVID-19 patients....

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Detalles Bibliográficos
Autores principales: Westmeier, Jaana, Paniskaki, Krystallenia, Karaköse, Zehra, Werner, Tanja, Sutter, Kathrin, Dolff, Sebastian, Overbeck, Marvin, Limmer, Andreas, Liu, Jia, Zheng, Xin, Brenner, Thorsten, Berger, Marc M., Witzke, Oliver, Trilling, Mirko, Lu, Mengji, Yang, Dongliang, Babel, Nina, Westhoff, Timm, Dittmer, Ulf, Zelinskyy, Gennadiy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7502863/
https://www.ncbi.nlm.nih.gov/pubmed/32948688
http://dx.doi.org/10.1128/mBio.02243-20
Descripción
Sumario:Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection induces a T cell response that most likely contributes to virus control in COVID-19 patients but may also induce immunopathology. Until now, the cytotoxic T cell response has not been very well characterized in COVID-19 patients. Here, we analyzed the differentiation and cytotoxic profile of T cells in 30 cases of mild COVID-19 during acute infection. SARS-CoV-2 infection induced a cytotoxic response of CD8(+) T cells, but not CD4(+) T cells, characterized by the simultaneous production of granzyme A and B as well as perforin within different effector CD8(+) T cell subsets. PD-1-expressing CD8(+) T cells also produced cytotoxic molecules during acute infection, indicating that they were not functionally exhausted. However, in COVID-19 patients over the age of 80 years, the cytotoxic T cell potential was diminished, especially in effector memory and terminally differentiated effector CD8(+) cells, showing that elderly patients have impaired cellular immunity against SARS-CoV-2. Our data provide valuable information about T cell responses in COVID-19 patients that may also have important implications for vaccine development.