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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2021
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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) |
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NK cells T cells immunology lung transplant cytomegalovirus Biology (General) QH301-705.5 |
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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 |
work_keys_str_mv |
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_version_ |
1718412639681380352 |