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Abstract In addition to CD4 + T cells and neutralizing antibodies, CD8 + T cells contribute to protective immune responses against SARS-CoV-2 in patients with coronavirus disease 2019 (COVID-19), an ongoing pandemic disease. In patients with COVID-19, CD8 + T cells exhibiting activated phenotypes are commonly observed, although the absolute number of CD8 + T cells is decreased. In addition, several studies have reported an upregulation of inhibitory immune checkpoint receptors, such as PD-1, and the expression of exhaustion-associated gene signatures in CD8 + T cells from patients with COVID-19. However, whether CD8 + T cells are truly exhausted during COVID-19 has been a controversial issue. In the present review, we summarize the current understanding of CD8 + T-cell exhaustion and describe the available knowledge on the phenotypes and functions of CD8 + T cells in the context of activation and exhaustion. We also summarize recent reports regarding phenotypical and functional analyses of SARS-CoV-2-specific CD8 + T cells and discuss long-term SARS-CoV-2-specific CD8 + T-cell memory.
Rha et al. (Thu,) studied this question.