Mucosal-associated invariant T (MAIT) cells mediate protective host responses in sepsis.

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Title: Mucosal-associated invariant T (MAIT) cells mediate protective host responses in sepsis.
Authors: Trivedi S; Division of Infectious Diseases, University of Utah, Salt Lake City, United States., Labuz D; Division of Infectious Diseases, University of Utah, Salt Lake City, United States., Anderson CP; Division of Infectious Diseases, University of Utah, Salt Lake City, United States., Araujo CV; Molecular Medicine Program, University of Utah, Salt Lake City, United States., Blair A; Molecular Medicine Program, University of Utah, Salt Lake City, United States., Middleton EA; Molecular Medicine Program, University of Utah, Salt Lake City, United States.; Division of Pulmonary and Critical Care, University of Utah, Salt Lake City, United States., Jensen O; Division of Infectious Diseases, University of Utah, Salt Lake City, United States., Tran A; Division of Microbiology and Immunology, Department of Pathology, University of Utah, Salt Lake City, United States., Mulvey MA; Division of Microbiology and Immunology, Department of Pathology, University of Utah, Salt Lake City, United States., Campbell RA; Molecular Medicine Program, University of Utah, Salt Lake City, United States.; Division of General Internal Medicine, Department of Internal Medicine, University of Utah, Salt Lake City, United States., Hale JS; Division of Microbiology and Immunology, Department of Pathology, University of Utah, Salt Lake City, United States., Rondina MT; Molecular Medicine Program, University of Utah, Salt Lake City, United States.; Division of General Internal Medicine, Department of Internal Medicine, University of Utah, Salt Lake City, United States.; George E. Wahlen VAMC Department of Internal Medicine and GRECC, University of Utah, Salt Lake City, United States., Leung DT; Division of Infectious Diseases, University of Utah, Salt Lake City, United States.; Division of Microbiology and Immunology, Department of Pathology, University of Utah, Salt Lake City, United States.
Source: ELife [Elife] 2020 Nov 09; Vol. 9. Date of Electronic Publication: 2020 Nov 09.
Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
Journal Info: Publisher: eLife Sciences Publications, Ltd Country of Publication: England NLM ID: 101579614 Publication Model: Electronic Cited Medium: Internet ISSN: 2050-084X (Electronic) Linking ISSN: 2050084X NLM ISO Abbreviation: Elife Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: Mucosal-associated invariant T (MAIT) cells mediate protective host responses in sepsis.
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  Data: <searchLink fieldCode="AU" term="%22Trivedi+S%22">Trivedi S</searchLink>; Division of Infectious Diseases, University of Utah, Salt Lake City, United States.<br /><searchLink fieldCode="AU" term="%22Labuz+D%22">Labuz D</searchLink>; Division of Infectious Diseases, University of Utah, Salt Lake City, United States.<br /><searchLink fieldCode="AU" term="%22Anderson+CP%22">Anderson CP</searchLink>; Division of Infectious Diseases, University of Utah, Salt Lake City, United States.<br /><searchLink fieldCode="AU" term="%22Araujo+CV%22">Araujo CV</searchLink>; Molecular Medicine Program, University of Utah, Salt Lake City, United States.<br /><searchLink fieldCode="AU" term="%22Blair+A%22">Blair A</searchLink>; Molecular Medicine Program, University of Utah, Salt Lake City, United States.<br /><searchLink fieldCode="AU" term="%22Middleton+EA%22">Middleton EA</searchLink>; Molecular Medicine Program, University of Utah, Salt Lake City, United States.; Division of Pulmonary and Critical Care, University of Utah, Salt Lake City, United States.<br /><searchLink fieldCode="AU" term="%22Jensen+O%22">Jensen O</searchLink>; Division of Infectious Diseases, University of Utah, Salt Lake City, United States.<br /><searchLink fieldCode="AU" term="%22Tran+A%22">Tran A</searchLink>; Division of Microbiology and Immunology, Department of Pathology, University of Utah, Salt Lake City, United States.<br /><searchLink fieldCode="AU" term="%22Mulvey+MA%22">Mulvey MA</searchLink>; Division of Microbiology and Immunology, Department of Pathology, University of Utah, Salt Lake City, United States.<br /><searchLink fieldCode="AU" term="%22Campbell+RA%22">Campbell RA</searchLink>; Molecular Medicine Program, University of Utah, Salt Lake City, United States.; Division of General Internal Medicine, Department of Internal Medicine, University of Utah, Salt Lake City, United States.<br /><searchLink fieldCode="AU" term="%22Hale+JS%22">Hale JS</searchLink>; Division of Microbiology and Immunology, Department of Pathology, University of Utah, Salt Lake City, United States.<br /><searchLink fieldCode="AU" term="%22Rondina+MT%22">Rondina MT</searchLink>; Molecular Medicine Program, University of Utah, Salt Lake City, United States.; Division of General Internal Medicine, Department of Internal Medicine, University of Utah, Salt Lake City, United States.; George E. Wahlen VAMC Department of Internal Medicine and GRECC, University of Utah, Salt Lake City, United States.<br /><searchLink fieldCode="AU" term="%22Leung+DT%22">Leung DT</searchLink>; Division of Infectious Diseases, University of Utah, Salt Lake City, United States.; Division of Microbiology and Immunology, Department of Pathology, University of Utah, Salt Lake City, United States.
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  Data: <searchLink fieldCode="JN" term="%22101579614%22">ELife</searchLink> [Elife] 2020 Nov 09; Vol. 9. <i>Date of Electronic Publication: </i>2020 Nov 09.
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