Metabolic programs define dysfunctional immune responses in severe COVID-19 patients.
Ontology highlight
ABSTRACT: It is unclear why some SARS-CoV-2 patients readily resolve infection while others develop severe disease. By interrogating metabolic programs of immune cells in severe and recovered coronavirus disease 2019 (COVID-19) patients compared with other viral infections, we identify a unique population of T cells. These T cells express increased Voltage-Dependent Anion Channel 1 (VDAC1), accompanied by gene programs and functional characteristics linked to mitochondrial dysfunction and apoptosis. The percentage of these cells increases in elderly patients and correlates with lymphopenia. Importantly, T cell apoptosis is inhibited in vitro by targeting the oligomerization of VDAC1 or blocking caspase activity. We also observe an expansion of myeloid-derived suppressor cells with unique metabolic p
SUBMITTER: Thompson EA
PROVIDER: S-EPMC7908880 | biostudies-literature | 2021 Mar
REPOSITORIES: biostudies-literature
ACCESS DATA