Attenuated Cd8+ T Cell Activation and Infiltration of the Lungs in Severe COVID-19 (preprint)

The SARS-CoV-2 genome encodes many proteins that directly compromise Type I interferon-mediated innate immunity. In acute COVID-19 the consequent dysregulated hyper-inflammatory state alters the milieu of draining lymph nodes and indirectly induces anatomically restricted, weeks-long transient defects in adaptive immunity. The striking attenuation of discrete aspects of T cell immunity may facilitate the evolution of more transmissible viral variants. No techniques employed to date, including single nuclear sequencing, have revealed information on pulmonary T cell subsets in severe COVID-19. Here we demonstrate an unexpected paucity of total CD8+T cells and CD8+Granzyme B+ T cells in the lung parenchyma in acute COVID-19. Apart from broadly compromising the generation of T FH cells in draining lymph nodes, acute COVID-19 is also linked to attenuated CD8+ T cell activation and infiltration of the lungs, and the delayed pulmonary accumulation of CD4+T cells with a cytotoxic phenotype.Funding Information: This work was supported by NIH U19 AI110495 to SP. Funding for these studies from the Massachusetts Consortium of Pathogen Readiness, the Mark and Lisa Schwartz Foundation and Enid Schwartz is also acknowledged.Declaration of Interests: SP is on the Scientific Advisory Board of Abpro Inc and BeBio. Thereare no other competing interests for any of the authors.Ethics Approval Statement: This study was conducted with the approval of the Institutional Review Boards at the Massachusetts General Hospital and the Brigham and Women’s Hospital.

Expansion of Cytotoxic CD4+ T cells in the lungs in severe COVID-19 (preprint)

The contributions of T cells infiltrating the lungs to SARS-CoV-2 clearance and disease progression are poorly understood. Although studies of CD8+ T cells in bronchoalveolar lavage and blood have suggested that these cells are exhausted in severe COVID-19, CD4+ T cells have not been systematically interrogated within the lung parenchyma. We establish here that cytotoxic CD4+ T cells (CD4+CTLs) are prominently expanded in the COVID-19 lung infiltrate. CD4+CTL numbers in the lung increase with disease severity and progression is accompanied by widespread HLA-DR expression on lung epithelial and endothelial cells, increased apoptosis of epithelial cells and tissue remodeling. Based on quantitative evidence for re-activation in the lung milieu, CD4+ CTLs are as likely to drive viral clearance as CD8+ T cells and may also be contributors to lung inflammation and eventually to fibrosis in severe COVID-19.

Expansion of Cytotoxic CD4+ T Cells in the Lungs in Severe COVID-19 (preprint)

The contributions of T cells infiltrating the lungs to SARS-CoV-2 clearance and disease progression are poorly understood. Although studies of CD8+ T cells in bronchoalveolar lavage and blood have suggested that these cells are exhausted in severe COVID-19, CD4+ T cells have not been systematically interrogated within the lung parenchyma. We establish here that cytotoxic CD4+ T cells (CD4+CTLs) are prominently expanded in the COVID-19 lung infiltrate. CD4+CTL numbers in the lung increase with disease severity and progression is accompanied by widespread HLA-DR expression on lung epithelial and endothelial cells, increased apoptosis of epithelial cells and tissue remodeling. Based on quantitative evidence for re-activation in the lung milieu, CD4+ CTLs are as likely to drive viral clearance as CD8+ T cells and may also be contributors to lung inflammation and eventually to fibrosis in severe COVID-19.Funding: This work was supported by NIH U19 AI110495 to SP. Funding for these studies from the Massachusetts Consortium of Pathogen Readiness, the Mark and Lisa Schwartz Foundation and Enid Schwartz is also acknowledged.Declaration of Interest: None to declare. Ethical Approval: This study was performed with the approval of the Institutional Review Boards at the Massachusetts General Hospital and the Brigham and Women’s Hospital.