RT Journal Article SR Electronic T1 Severely ill COVID-19 patients display augmented functional properties in SARS-CoV-2-reactive CD8+ T cells JF bioRxiv FD Cold Spring Harbor Laboratory SP 2020.07.09.194027 DO 10.1101/2020.07.09.194027 A1 Anthony Kusnadi A1 Ciro Ramírez-Suástegui A1 Vicente Fajardo A1 Serena J Chee A1 Benjamin J Meckiff A1 Hayley Simon A1 Emanuela Pelosi A1 Grégory Seumois A1 Ferhat Ay A1 Pandurangan Vijayanand A1 Christian H Ottensmeier YR 2020 UL http://biorxiv.org/content/early/2020/07/10/2020.07.09.194027.abstract AB The molecular properties of CD8+ T cells that respond to SARS-CoV-2 infection are not fully known. Here, we report on the single-cell transcriptomes of >80,000 virus-reactive CD8+ T cells from 39 COVID-19 patients and 10 healthy subjects. COVID-19 patients segregated into two groups based on whether the dominant CD8+ T cell response to SARS-CoV-2 was ‘exhausted’ or not. SARS-CoV-2-reactive cells in the exhausted subset were increased in frequency and displayed lesser cytotoxicity and inflammatory features in COVID-19 patients with mild compared to severe illness. In contrast, SARS-CoV-2-reactive cells in the non-exhausted subsets from patients with severe disease showed enrichment of transcripts linked to co-stimulation, pro-survival NF-κB signaling, and anti-apoptotic pathways, suggesting the generation of robust CD8+ T cell memory responses in patients with severe COVID-19 illness. CD8+ T cells reactive to influenza and respiratory syncytial virus from healthy subjects displayed polyfunctional features. Cells with such features were mostly absent in SARS-CoV-2 responsive cells from both COVID-19 patients and healthy controls non-exposed to SARS-CoV-2. Overall, our single-cell analysis revealed substantial diversity in the nature of CD8+ T cells responding to SARS-CoV-2.Competing Interest StatementThe authors have declared no competing interest.