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Contributions of neutrophils to the adaptive immune response in autoimmune disease

Neutrophils are granulocytic cytotoxic leukocytes of the innate immune system that activate during acute inflammation. Neutrophils can also persist beyond the acute phase of inflammation to impact the adaptive immune response during chronic inflammation. In the context of the autoimmune disease, neu...

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Detalles Bibliográficos
Autores principales: Pietrosimone, Kathryn M, Liu, Peng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4816207/
https://www.ncbi.nlm.nih.gov/pubmed/27042404
http://dx.doi.org/10.5528/wjtm.v4.i3.60
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author Pietrosimone, Kathryn M
Liu, Peng
author_facet Pietrosimone, Kathryn M
Liu, Peng
author_sort Pietrosimone, Kathryn M
collection PubMed
description Neutrophils are granulocytic cytotoxic leukocytes of the innate immune system that activate during acute inflammation. Neutrophils can also persist beyond the acute phase of inflammation to impact the adaptive immune response during chronic inflammation. In the context of the autoimmune disease, neutrophils modulating T and B cell functions by producing cytokines and chemokines, forming neutrophil extracellular traps, and acting as or priming antigen presentation cells. Thus, neutrophils are actively involved in chronic inflammation and tissue damage in autoimmune disease. Using rheumatoid arthritis as an example, this review focuses on functions of neutrophils in adaptive immunity and the therapeutic potential of these cells in the treatment of autoimmune disease and chronic inflammation.
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spelling pubmed-48162072016-03-31 Contributions of neutrophils to the adaptive immune response in autoimmune disease Pietrosimone, Kathryn M Liu, Peng World J Transl Med Article Neutrophils are granulocytic cytotoxic leukocytes of the innate immune system that activate during acute inflammation. Neutrophils can also persist beyond the acute phase of inflammation to impact the adaptive immune response during chronic inflammation. In the context of the autoimmune disease, neutrophils modulating T and B cell functions by producing cytokines and chemokines, forming neutrophil extracellular traps, and acting as or priming antigen presentation cells. Thus, neutrophils are actively involved in chronic inflammation and tissue damage in autoimmune disease. Using rheumatoid arthritis as an example, this review focuses on functions of neutrophils in adaptive immunity and the therapeutic potential of these cells in the treatment of autoimmune disease and chronic inflammation. 2015-12-12 2015-12 /pmc/articles/PMC4816207/ /pubmed/27042404 http://dx.doi.org/10.5528/wjtm.v4.i3.60 Text en http://creativecommons.org/licenses/by-nc/4.0/ This article is an open−access article which was selected by an in−house editor and fully peer−reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY−NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non−commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non−commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
spellingShingle Article
Pietrosimone, Kathryn M
Liu, Peng
Contributions of neutrophils to the adaptive immune response in autoimmune disease
title Contributions of neutrophils to the adaptive immune response in autoimmune disease
title_full Contributions of neutrophils to the adaptive immune response in autoimmune disease
title_fullStr Contributions of neutrophils to the adaptive immune response in autoimmune disease
title_full_unstemmed Contributions of neutrophils to the adaptive immune response in autoimmune disease
title_short Contributions of neutrophils to the adaptive immune response in autoimmune disease
title_sort contributions of neutrophils to the adaptive immune response in autoimmune disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4816207/
https://www.ncbi.nlm.nih.gov/pubmed/27042404
http://dx.doi.org/10.5528/wjtm.v4.i3.60
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