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Clinical outcome prediction in COVID-19 patients by lymphocyte subsets analysis and monocytes’ iTNF-α expression

Authors :
Luigi Atripaldi
Anna D'Antonio
Caterina Pirozzi
Paolo A. Ascierto
Lucia Festino
Chiara De Falco
Gerardo Botti
Pellegrino Cerino
Marcello Raffone
Silvia Sale
Marcello Curvietto
Mariaelena Capone
Umberto Atripaldi
Vito Vanella
Roberto Parrella
Luigi Scarpato
Valentina Santocchio
Gabriele Madonna
Francesco Perna
Michela Spatarella
Rocco Sabatino
Giuseppe Fiorentino
Tiziana Di Matola
Lidia Atripaldi
Vincenzo Montesarchio
Marco Palla
Antonio M. Grimaldi
Madonna, G.
Sale, S.
Capone, M.
De Falco, C.
Santocchio, V.
Di Matola, T.
Fiorentino, G.
Pirozzi, C.
D'Antonio, A.
Sabatino, R.
Atripaldi, L.
Atripaldi, U.
Raffone, M.
Curvietto, M.
Grimaldi, A. M.
Vanella, V.
Festino, L.
Scarpato, L.
Palla, M.
Spatarella, M.
Perna, F.
Cerino, P.
Botti, G.
Parrella, R.
Montesarchio, V.
Ascierto, P. A.
Source :
Biology, Volume 10, Issue 8, Biology, Vol 10, Iss 735, p 735 (2021)
Publication Year :
2021

Abstract

Simple Summary Several studies have explored the role of the inflammatory cells and cytokines involved in the protection or pathogenesis of coronavirus disease 2019. Unfortunately, the results have been controversial, and further studies are needed to better understand not only the roles but also the balance of these parameters, which are crucial data to improve prevention and treatment. As COVID-19 has a well-determined phasic progression and rapidly deteriorates approximately seven days after the onset of symptoms, it is extremely necessary to detect the clinical signs that are predictive of the outcome as early as possible. To this end, in this preliminary study, we evaluated the data relating to the monocyte intracellular TNF-α expression and lymphocyte subpopulations in peripheral blood collected from patients at admission and every day of hospitalization until day 7. Our findings point to a modulation of the different cellular mediators of the immune system, which probably play a key role in the outcome of the coronavirus disease 2019. Abstract In December 2019, a novel coronavirus, “SARS-CoV-2”, was recognized as the cause of coronavirus disease 2019 (COVID-19). Several studies have explored the changes and the role of inflammatory cells and cytokines in the immunopathogenesis of the disease, but until today, the results have been controversial. Based on these premises, we conducted a retrospective assessment of monocyte intracellular TNF-α expression (iTNF-α) and on the frequencies of lymphocyte sub-populations in twenty-five patients with moderate/severe COVID-19. We found lymphopenia in all COVID-19 infected subjects compared to healthy subjects. On initial observation, in patients with favorable outcomes, we detected a high absolute eosinophil count and a high CD4+/CD8+ T lymphocytes ratio, while in the Exitus Group, we observed high neutrophil and CD8+ T lymphocyte counts. During infection, in patients with favorable outcomes, we observed a rise in the lymphocyte count, in the monocyte and in Treg lymphocyte counts, and in the CD4+ and in CD8+ T lymphocytes count but a reduction in the CD4+/CD8+ T lymphocyte ratio. Instead, in the Exitus Group, we observed a reduction in the Treg lymphocyte counts and a decrease in iTNF-α expression. Our preliminary findings point to a modulation of the different cellular mediators of the immune system, which probably play a key role in the outcomes of COVID-19.

Details

Language :
English
Database :
OpenAIRE
Journal :
Biology, Volume 10, Issue 8, Biology, Vol 10, Iss 735, p 735 (2021)
Accession number :
edsair.doi.dedup.....654a955a39042645e51a40b5c0307df7