Abstract
COVID-19 manifests with a wide diversity of clinical phenotypes characterized by
dysfunctional and exaggerated host immune responses. Many results have been
described on the status of the immune system of patients infected with SARS-CoV-2,
but there are still aspects that have not been fully characterized or understood. In this
study, we have analyzed a cohort of patients with mild, moderate and severe disease.We
performed flow cytometric studies and correlated the data with the clinical characteristics
and clinical laboratory values of the patients. Both conventional and unsupervised data
analyses concluded that patients with severe disease are characterized, among others,
by a higher state of activation in all T cell subsets (CD4, CD8, double negative and
T follicular helper cells), higher expression of perforin and granzyme B in cytotoxic
cells, expansion of adaptive NK cells and the accumulation of activated and immature
dysfunctional monocytes which are identified by a low expression of HLA-DR and an
intriguing shift in the expression pattern of CD300 receptors.More importantly, correlation
analysis showed a strong association between the alterations in the immune cells and
the clinical signs of severity. These results indicate that patients with severe COVID-19
have a broad perturbation of their immune system, and they will help to understand the
immunopathogenesis of COVID-19.