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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.
  • Yu C; Department of Ophthalmology, Duke University School of Medicine, Durham, NC 27710, USA.
  • Littleton S; Department of Ophthalmology, Duke University School of Medicine, Durham, NC 27710, USA.
  • Giroux NS; Department of Immunology, Duke University School of Medicine, Durham, NC 27710, USA.
  • Mathew R; Department of Biomedical Engineering, Pratt School of Engineering, Duke University, Durham, NC 27710, USA.
  • Ding S; Department of Ophthalmology, Duke University School of Medicine, Durham, NC 27710, USA.
  • Kalnitsky J; Department of Biomedical Engineering, Pratt School of Engineering, Duke University, Durham, NC 27710, USA.
  • Yang Y; Department of Ophthalmology, Duke University School of Medicine, Durham, NC 27710, USA.
  • Petzold E; Department of Pathology and Laboratory Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
  • Chung HA; McAllister Heart Institute, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
  • Rivera GO; Center for Applied Genomics and Precision Medicine, Duke University, Durham, NC 27710, USA.
  • Rotstein T; Department of Biomedical Engineering, Pratt School of Engineering, Duke University, Durham, NC 27710, USA.
  • Xi R; Department of Biomedical Engineering, Pratt School of Engineering, Duke University, Durham, NC 27710, USA.
  • Ko ER; Department of Biomedical Engineering, Pratt School of Engineering, Duke University, Durham, NC 27710, USA.
  • Tsalik EL; Department of Biomedical Engineering, Pratt School of Engineering, Duke University, Durham, NC 27710, USA.
  • Sempowski GD; Center for Applied Genomics and Precision Medicine, Duke University, Durham, NC 27710, USA.
  • Denny TN; Duke Department of Medicine, Duke University School of Medicine, Durham, NC 27710, USA.
  • Burke TW; Center for Applied Genomics and Precision Medicine, Duke University, Durham, NC 27710, USA.
  • McClain MT; Durham Veterans Affairs Health Care System, Durham, NC 27705, USA.
  • Woods CW; Division of Infectious Diseases, Duke University Medical Center, Durham, NC 27710, USA.
  • Shen X; Duke Human Vaccine Institute, Duke University Medical Center, Durham, NC 27710, USA.
  • Saban DR; Duke Human Vaccine Institute, Duke University Medical Center, Durham, NC 27710, USA.
Med (N Y) ; 2(6): 755-772.e5, 2021 06 11.
Article in English | MEDLINE | ID: covidwho-1300946
ABSTRACT

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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Full text: Available Collection: International databases Database: MEDLINE Main subject: Mucosal-Associated Invariant T Cells / COVID-19 Limits: Female / Humans / Male Country/Region as subject: North America Language: English Journal: Med (N Y) Year: 2021 Document Type: Article Affiliation country: J.medj.2021.04.008

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Mucosal-Associated Invariant T Cells / COVID-19 Limits: Female / Humans / Male Country/Region as subject: North America Language: English Journal: Med (N Y) Year: 2021 Document Type: Article Affiliation country: J.medj.2021.04.008