NK and T Cell Immunological Signatures in Hospitalized Patients with COVID-19

Severe acute respiratory syndrome caused by coronavirus 2 emerged in Wuhan (China) in December 2019 and has severely challenged the human population. NK and T cells are involved in the progression of COVID-19 infection through the ability of NK cells to modulate T-cell responses, and by the stimulat...

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Autores principales: Laura Bergantini, Miriana d'Alessandro, Paolo Cameli, Dalila Cavallaro, Sara Gangi, Behar Cekorja, Piersante Sestini, Elena Bargagli
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Publicado: MDPI AG 2021
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spelling oai:doaj.org-article:31df8d5065e14aaea97a56c64c2336922021-11-25T17:12:26ZNK and T Cell Immunological Signatures in Hospitalized Patients with COVID-1910.3390/cells101131822073-4409https://doaj.org/article/31df8d5065e14aaea97a56c64c2336922021-11-01T00:00:00Zhttps://www.mdpi.com/2073-4409/10/11/3182https://doaj.org/toc/2073-4409Severe acute respiratory syndrome caused by coronavirus 2 emerged in Wuhan (China) in December 2019 and has severely challenged the human population. NK and T cells are involved in the progression of COVID-19 infection through the ability of NK cells to modulate T-cell responses, and by the stimulation of cytokine release. No detailed investigation of the NK cell landscape in clinical SARS-CoV-2 infection has yet been reported. A total of 35 COVID-19 hospitalised patients were stratified for clinical severity and 17 healthy subjects were enrolled. NK cell subsets and T cell subsets were analysed with flow cytometry. Serum cytokines were detected with a bead-based multiplex assay. Fewer CD56<sup>dim</sup>CD16<sup>bright</sup>NKG2A<sup>+</sup>NK cells and a parallel increase in the CD56<sup>+</sup>CD69<sup>+</sup>NK, CD56<sup>+</sup>PD-1<sup>+</sup>NK, CD56<sup>+</sup>NKp44<sup>+</sup>NK subset were reported in COVID-19 than HC. A significantly higher adaptive/memory-like NK cell frequency in patients with severe disease than in those with mild and moderate phenotypes were reported. Moreover, adaptive/memory-like NK cell frequencies were significantly higher in patients who died than in survivors. Severe COVID-19 patients showed higher serum concentrations of IL-6 than mild and control groups. Direct correlation emerged for IL-6 and adaptive/memory-like NK. All these findings provide new insights into the immune response of patients with COVID-19. In particular, they demonstrate activation of NK through overexpression of CD69 and CD25 and show that PD-1 inhibitory signalling maintains an exhausted phenotype in NK cells. These results suggest that adaptive/memory-like NK cells could be the basis of promising targeted therapy for future viral infections.Laura BergantiniMiriana d'AlessandroPaolo CameliDalila CavallaroSara GangiBehar CekorjaPiersante SestiniElena BargagliMDPI AGarticleNK cellsT cellsimmunologylung transplantcytomegalovirusBiology (General)QH301-705.5ENCells, Vol 10, Iss 3182, p 3182 (2021)
institution DOAJ
collection DOAJ
language EN
topic NK cells
T cells
immunology
lung transplant
cytomegalovirus
Biology (General)
QH301-705.5
spellingShingle NK cells
T cells
immunology
lung transplant
cytomegalovirus
Biology (General)
QH301-705.5
Laura Bergantini
Miriana d'Alessandro
Paolo Cameli
Dalila Cavallaro
Sara Gangi
Behar Cekorja
Piersante Sestini
Elena Bargagli
NK and T Cell Immunological Signatures in Hospitalized Patients with COVID-19
description Severe acute respiratory syndrome caused by coronavirus 2 emerged in Wuhan (China) in December 2019 and has severely challenged the human population. NK and T cells are involved in the progression of COVID-19 infection through the ability of NK cells to modulate T-cell responses, and by the stimulation of cytokine release. No detailed investigation of the NK cell landscape in clinical SARS-CoV-2 infection has yet been reported. A total of 35 COVID-19 hospitalised patients were stratified for clinical severity and 17 healthy subjects were enrolled. NK cell subsets and T cell subsets were analysed with flow cytometry. Serum cytokines were detected with a bead-based multiplex assay. Fewer CD56<sup>dim</sup>CD16<sup>bright</sup>NKG2A<sup>+</sup>NK cells and a parallel increase in the CD56<sup>+</sup>CD69<sup>+</sup>NK, CD56<sup>+</sup>PD-1<sup>+</sup>NK, CD56<sup>+</sup>NKp44<sup>+</sup>NK subset were reported in COVID-19 than HC. A significantly higher adaptive/memory-like NK cell frequency in patients with severe disease than in those with mild and moderate phenotypes were reported. Moreover, adaptive/memory-like NK cell frequencies were significantly higher in patients who died than in survivors. Severe COVID-19 patients showed higher serum concentrations of IL-6 than mild and control groups. Direct correlation emerged for IL-6 and adaptive/memory-like NK. All these findings provide new insights into the immune response of patients with COVID-19. In particular, they demonstrate activation of NK through overexpression of CD69 and CD25 and show that PD-1 inhibitory signalling maintains an exhausted phenotype in NK cells. These results suggest that adaptive/memory-like NK cells could be the basis of promising targeted therapy for future viral infections.
format article
author Laura Bergantini
Miriana d'Alessandro
Paolo Cameli
Dalila Cavallaro
Sara Gangi
Behar Cekorja
Piersante Sestini
Elena Bargagli
author_facet Laura Bergantini
Miriana d'Alessandro
Paolo Cameli
Dalila Cavallaro
Sara Gangi
Behar Cekorja
Piersante Sestini
Elena Bargagli
author_sort Laura Bergantini
title NK and T Cell Immunological Signatures in Hospitalized Patients with COVID-19
title_short NK and T Cell Immunological Signatures in Hospitalized Patients with COVID-19
title_full NK and T Cell Immunological Signatures in Hospitalized Patients with COVID-19
title_fullStr NK and T Cell Immunological Signatures in Hospitalized Patients with COVID-19
title_full_unstemmed NK and T Cell Immunological Signatures in Hospitalized Patients with COVID-19
title_sort nk and t cell immunological signatures in hospitalized patients with covid-19
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/31df8d5065e14aaea97a56c64c233692
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