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Mucosal-associated invariant T cell responses differ by sex in COVID-19

BACKGROUND: Sexual dimorphisms in immune responses contribute to coronavirus disease 2019 (COVID-19) outcomes, but the mechanisms governing this disparity remain incompletely understood. METHODS: We carried out sex-balanced sampling of peripheral blood mononuclear cells from hospitalized and non-hos...

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Autores principales: Yu, Chen, Littleton, Sejiro, Giroux, Nicholas S., Mathew, Rose, Ding, Shengli, Kalnitsky, Joan, Yang, Yuchen, Petzold, Elizabeth, Chung, Hong A., Rivera, Grecia O., Rotstein, Tomer, Xi, Rui, Ko, Emily R., Tsalik, Ephraim L., Sempowski, Gregory D., Denny, Thomas N., Burke, Thomas W., McClain, Micah T., Woods, Christopher W., Shen, Xiling, Saban, Daniel R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8043578/
https://www.ncbi.nlm.nih.gov/pubmed/33870241
http://dx.doi.org/10.1016/j.medj.2021.04.008
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author Yu, Chen
Littleton, Sejiro
Giroux, Nicholas S.
Mathew, Rose
Ding, Shengli
Kalnitsky, Joan
Yang, Yuchen
Petzold, Elizabeth
Chung, Hong A.
Rivera, Grecia O.
Rotstein, Tomer
Xi, Rui
Ko, Emily R.
Tsalik, Ephraim L.
Sempowski, Gregory D.
Denny, Thomas N.
Burke, Thomas W.
McClain, Micah T.
Woods, Christopher W.
Shen, Xiling
Saban, Daniel R.
author_facet Yu, Chen
Littleton, Sejiro
Giroux, Nicholas S.
Mathew, Rose
Ding, Shengli
Kalnitsky, Joan
Yang, Yuchen
Petzold, Elizabeth
Chung, Hong A.
Rivera, Grecia O.
Rotstein, Tomer
Xi, Rui
Ko, Emily R.
Tsalik, Ephraim L.
Sempowski, Gregory D.
Denny, Thomas N.
Burke, Thomas W.
McClain, Micah T.
Woods, Christopher W.
Shen, Xiling
Saban, Daniel R.
author_sort Yu, Chen
collection PubMed
description BACKGROUND: Sexual dimorphisms in immune responses contribute to coronavirus disease 2019 (COVID-19) outcomes, but the mechanisms governing this disparity remain incompletely understood. METHODS: We carried out sex-balanced sampling of peripheral blood mononuclear cells from hospitalized and non-hospitalized individuals with confirmed COVID-19, uninfected close contacts, and healthy control individuals for 36-color flow cytometry and single-cell RNA sequencing. FINDINGS: Our results revealed a pronounced reduction of circulating mucosal-associated invariant T (MAIT) cells in infected females. Integration of published COVID-19 airway tissue datasets suggests that this reduction represented a major wave of MAIT cell extravasation during early infection in females. Moreover, MAIT cells from females possessed an immunologically active gene signature, whereas cells from males were pro-apoptotic. CONCLUSIONS: Our findings uncover a female-specific protective MAIT cell profile, potentially shedding light on reduced COVID-19 susceptibility in females. FUNDING: This work was supported by NIH/NIAID (U01AI066569 and UM1AI104681), the Defense Advanced Projects Agency (DARPA; N66001-09-C-2082 and HR0011-17-2-0069), the Veterans Affairs Health System, and Virology Quality Assurance (VQA; 75N93019C00015). The content is solely the responsibility of the authors and does not necessarily represent the official view of the National Institutes of Health. COVID-19 samples were processed under Biosafety level 2 (BSL-2) with aerosol management enhancement or BSL-3 in the Duke Regional Biocontainment Laboratory, which received partial support for construction from NIH/NIAID (UC6AI058607).
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spelling pubmed-80435782021-04-14 Mucosal-associated invariant T cell responses differ by sex in COVID-19 Yu, Chen Littleton, Sejiro Giroux, Nicholas S. Mathew, Rose Ding, Shengli Kalnitsky, Joan Yang, Yuchen Petzold, Elizabeth Chung, Hong A. Rivera, Grecia O. Rotstein, Tomer Xi, Rui Ko, Emily R. Tsalik, Ephraim L. Sempowski, Gregory D. Denny, Thomas N. Burke, Thomas W. McClain, Micah T. Woods, Christopher W. Shen, Xiling Saban, Daniel R. Med (N Y) Clinical and Translational Article BACKGROUND: Sexual dimorphisms in immune responses contribute to coronavirus disease 2019 (COVID-19) outcomes, but the mechanisms governing this disparity remain incompletely understood. METHODS: We carried out sex-balanced sampling of peripheral blood mononuclear cells from hospitalized and non-hospitalized individuals with confirmed COVID-19, uninfected close contacts, and healthy control individuals for 36-color flow cytometry and single-cell RNA sequencing. FINDINGS: Our results revealed a pronounced reduction of circulating mucosal-associated invariant T (MAIT) cells in infected females. Integration of published COVID-19 airway tissue datasets suggests that this reduction represented a major wave of MAIT cell extravasation during early infection in females. Moreover, MAIT cells from females possessed an immunologically active gene signature, whereas cells from males were pro-apoptotic. CONCLUSIONS: Our findings uncover a female-specific protective MAIT cell profile, potentially shedding light on reduced COVID-19 susceptibility in females. FUNDING: This work was supported by NIH/NIAID (U01AI066569 and UM1AI104681), the Defense Advanced Projects Agency (DARPA; N66001-09-C-2082 and HR0011-17-2-0069), the Veterans Affairs Health System, and Virology Quality Assurance (VQA; 75N93019C00015). The content is solely the responsibility of the authors and does not necessarily represent the official view of the National Institutes of Health. COVID-19 samples were processed under Biosafety level 2 (BSL-2) with aerosol management enhancement or BSL-3 in the Duke Regional Biocontainment Laboratory, which received partial support for construction from NIH/NIAID (UC6AI058607). Elsevier Inc. 2021-06-11 2021-04-13 /pmc/articles/PMC8043578/ /pubmed/33870241 http://dx.doi.org/10.1016/j.medj.2021.04.008 Text en © 2021 Elsevier Inc. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Clinical and Translational Article
Yu, Chen
Littleton, Sejiro
Giroux, Nicholas S.
Mathew, Rose
Ding, Shengli
Kalnitsky, Joan
Yang, Yuchen
Petzold, Elizabeth
Chung, Hong A.
Rivera, Grecia O.
Rotstein, Tomer
Xi, Rui
Ko, Emily R.
Tsalik, Ephraim L.
Sempowski, Gregory D.
Denny, Thomas N.
Burke, Thomas W.
McClain, Micah T.
Woods, Christopher W.
Shen, Xiling
Saban, Daniel R.
Mucosal-associated invariant T cell responses differ by sex in COVID-19
title Mucosal-associated invariant T cell responses differ by sex in COVID-19
title_full Mucosal-associated invariant T cell responses differ by sex in COVID-19
title_fullStr Mucosal-associated invariant T cell responses differ by sex in COVID-19
title_full_unstemmed Mucosal-associated invariant T cell responses differ by sex in COVID-19
title_short Mucosal-associated invariant T cell responses differ by sex in COVID-19
title_sort mucosal-associated invariant t cell responses differ by sex in covid-19
topic Clinical and Translational Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8043578/
https://www.ncbi.nlm.nih.gov/pubmed/33870241
http://dx.doi.org/10.1016/j.medj.2021.04.008
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