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CD1d- and MR1-Restricted T Cells in Sepsis

Dysregulated immune responses to infection, such as those encountered in sepsis, can be catastrophic. Sepsis is typically triggered by an overwhelming systemic response to an infectious agent(s) and is associated with high morbidity and mortality even under optimal critical care. Recent studies have...

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Autores principales: Szabo, Peter A., Anantha, Ram V., Shaler, Christopher R., McCormick, John K., Haeryfar, S.M. Mansour
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4533011/
https://www.ncbi.nlm.nih.gov/pubmed/26322041
http://dx.doi.org/10.3389/fimmu.2015.00401
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author Szabo, Peter A.
Anantha, Ram V.
Shaler, Christopher R.
McCormick, John K.
Haeryfar, S.M. Mansour
author_facet Szabo, Peter A.
Anantha, Ram V.
Shaler, Christopher R.
McCormick, John K.
Haeryfar, S.M. Mansour
author_sort Szabo, Peter A.
collection PubMed
description Dysregulated immune responses to infection, such as those encountered in sepsis, can be catastrophic. Sepsis is typically triggered by an overwhelming systemic response to an infectious agent(s) and is associated with high morbidity and mortality even under optimal critical care. Recent studies have implicated unconventional, innate-like T lymphocytes, including CD1d- and MR1-restricted T cells as effectors and/or regulators of inflammatory responses during sepsis. These cell types are typified by invariant natural killer T (iNKT) cells, variant NKT (vNKT) cells, and mucosa-associated invariant T (MAIT) cells. iNKT and vNKT cells are CD1d-restricted, lipid-reactive cells with remarkable immunoregulatory properties. MAIT cells participate in antimicrobial defense, and are restricted by major histocompatibility complex-related protein 1 (MR1), which displays microbe-derived vitamin B metabolites. Importantly, NKT and MAIT cells are rapid and potent producers of immunomodulatory cytokines. Therefore, they may be considered attractive targets during the early hyperinflammatory phase of sepsis when immediate interventions are urgently needed, and also in later phases when adjuvant immunotherapies could potentially reverse the dangerous state of immunosuppression. We will highlight recent findings that point to the significance or the therapeutic potentials of NKT and MAIT cells in sepsis and will also discuss what lies ahead in research in this area.
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spelling pubmed-45330112015-08-28 CD1d- and MR1-Restricted T Cells in Sepsis Szabo, Peter A. Anantha, Ram V. Shaler, Christopher R. McCormick, John K. Haeryfar, S.M. Mansour Front Immunol Immunology Dysregulated immune responses to infection, such as those encountered in sepsis, can be catastrophic. Sepsis is typically triggered by an overwhelming systemic response to an infectious agent(s) and is associated with high morbidity and mortality even under optimal critical care. Recent studies have implicated unconventional, innate-like T lymphocytes, including CD1d- and MR1-restricted T cells as effectors and/or regulators of inflammatory responses during sepsis. These cell types are typified by invariant natural killer T (iNKT) cells, variant NKT (vNKT) cells, and mucosa-associated invariant T (MAIT) cells. iNKT and vNKT cells are CD1d-restricted, lipid-reactive cells with remarkable immunoregulatory properties. MAIT cells participate in antimicrobial defense, and are restricted by major histocompatibility complex-related protein 1 (MR1), which displays microbe-derived vitamin B metabolites. Importantly, NKT and MAIT cells are rapid and potent producers of immunomodulatory cytokines. Therefore, they may be considered attractive targets during the early hyperinflammatory phase of sepsis when immediate interventions are urgently needed, and also in later phases when adjuvant immunotherapies could potentially reverse the dangerous state of immunosuppression. We will highlight recent findings that point to the significance or the therapeutic potentials of NKT and MAIT cells in sepsis and will also discuss what lies ahead in research in this area. Frontiers Media S.A. 2015-08-12 /pmc/articles/PMC4533011/ /pubmed/26322041 http://dx.doi.org/10.3389/fimmu.2015.00401 Text en Copyright © 2015 Szabo, Anantha, Shaler, McCormick and Haeryfar. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Szabo, Peter A.
Anantha, Ram V.
Shaler, Christopher R.
McCormick, John K.
Haeryfar, S.M. Mansour
CD1d- and MR1-Restricted T Cells in Sepsis
title CD1d- and MR1-Restricted T Cells in Sepsis
title_full CD1d- and MR1-Restricted T Cells in Sepsis
title_fullStr CD1d- and MR1-Restricted T Cells in Sepsis
title_full_unstemmed CD1d- and MR1-Restricted T Cells in Sepsis
title_short CD1d- and MR1-Restricted T Cells in Sepsis
title_sort cd1d- and mr1-restricted t cells in sepsis
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4533011/
https://www.ncbi.nlm.nih.gov/pubmed/26322041
http://dx.doi.org/10.3389/fimmu.2015.00401
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