Critically ill COVID-19 patients exhibit hyperactive cytokine responses associated with effector exhausted senescent T cells in acute infection

Arcanjo, Angélica; Pinto, Kamila Guimarães; Logullo, Jorgete; Leite, Paulo Emílio Corrêa; Menezes, Camilla Cristie Barreto; Freire-de-Lima, Leonardo; Diniz-Lima, Israel; Decoté-Ricardo, Debora; Rodrigues-da-Silva, Rodrigo Nunes; Freire-de-Lima, Celio Geraldo; Filardy, Alessandra Almeida; Lima-Junior, Josué da Costa; Bertho, Alvaro Luiz; De Luca, Paula Mello; Granjeiro, José Mauro; Barroso, Shana Priscila Coutinho; Conceição-Silva, Fátima; Savino, Wilson; Morrot, Alexandre

COVID-19 can progress to severe pneumonia with respiratory failure and is aggravated by the deregulation of the immune system causing an excessive inflammation including the cytokine storm. We herein report that severe acutely infected patients have high levels of both type-1 and type-2 cytokines. Our results show abnormal cytokine levels upon T cell stimulation, in a non-polarized profile. Furthermore, our findings indicate that this hyperactive cytokine response is associated with a significantly increased frequency of late-differentiated T cells with particular phenotype of effector exhausted/senescent CD28 (-)CD57 (+) cells. Interestingly, we demonstrated for the first time an increased frequency of CD3 (+)CD4 (+)CD28 (-)CD57 (+) T cells with expression of programmed death 1 (PD-1), one of the hallmarks of T cell exhaustion. These findings reveal that COVID-19 is associated with acute immunodeficiency, especially within the CD4 (+) T cell compartment and points to possible mechanisms of loss of clonal repertoire and susceptibility to viral relapse and reinfection events.