| Literature DB >> 30554082 |
Edy Yong Kim1, William M Oldham2.
Abstract
Rapid onset of acute inflammation is a hallmark of critical illnesses that bring patients to the intensive care unit (ICU). In critical illness, innate T cells rapidly reach full activation and drive a robust acute inflammatory response. As "cellular adjuvants," innate T cells worsen inflammation and mortality in several common critical illnesses including sepsis, ischemia-reperfusion injury, stroke, and exacerbations of respiratory disease. Interestingly, innate T cell subsets can also promote a protective and anti-inflammatory response in sepsis, ischemia-reperfusion injury, and asthma. Therapies that target innate T cells have been validated in several models of critical illness. Here, we review the role of natural killer T (NKT) cells, mucosal-associated invariant T (MAIT) cells and γδ T cells in clinical and experimental critical illness.Entities:
Keywords: Cardiac arrest; Critical care; Gamma delta T cell; MAIT cell; NKT cell; Sepsis
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Year: 2018 PMID: 30554082 PMCID: PMC6331274 DOI: 10.1016/j.molimm.2018.09.026
Source DB: PubMed Journal: Mol Immunol ISSN: 0161-5890 Impact factor: 4.407