Selected article for: "blood sampling and flow cytometry"

Author: Yu, Chen; Littleton, Sejiro; Giroux, Nicholas; Mathew, Rose; Ding, Shengli; Kalnitsky, Joan; Petzold, Elizabeth W.; Chung, Hong; Palomino, Grecia Rivera; 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.
Title: Mucosal Associated Invariant T (MAIT) Cell Responses Differ by Sex in COVID-19
  • Cord-id: ee8bzn2l
  • Document date: 2020_12_1
  • ID: ee8bzn2l
    Snippet: Sexual dimorphisms in immune responses contribute to coronavirus disease 2019 (COVID-19) outcomes, yet the mechanisms governing this disparity remain incompletely understood. We carried out sex-balanced sampling of peripheral blood mononuclear cells from confirmed COVID-19 inpatients and outpatients, uninfected close contacts, and healthy controls for 36-color flow cytometry and single cell RNA-sequencing. Our results revealed a pronounced reduction of circulating mucosal associated invariant T
    Document: Sexual dimorphisms in immune responses contribute to coronavirus disease 2019 (COVID-19) outcomes, yet the mechanisms governing this disparity remain incompletely understood. We carried out sex-balanced sampling of peripheral blood mononuclear cells from confirmed COVID-19 inpatients and outpatients, uninfected close contacts, and healthy controls for 36-color flow cytometry and single cell RNA-sequencing. 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 implicate that this reduction represented a major wave of MAIT cell extravasation during early infection in females. Moreover, female MAIT cells possessed an immunologically active gene signature, whereas male counterparts were pro-apoptotic. Collectively, our findings uncover a female-specific protective MAIT profile, potentially shedding light on reduced COVID-19 susceptibility in females.

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