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Group 2 Innate Lymphoid Cells (ILC2): Type 2 Immunity and Helminth Immunity
Group 2 innate lymphoid cells (ILC2) have emerged as a major component of type 2 inflammation in mice and humans. ILC2 secrete large amounts of interleukins 5 and 13, which are largely responsible for host protective immunity against helminth parasites because these cytokines induce profound changes...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6539149/ https://www.ncbi.nlm.nih.gov/pubmed/31072011 http://dx.doi.org/10.3390/ijms20092276 |
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author | Herbert, De’Broski R. Douglas, Bonnie Zullo, Kelly |
author_facet | Herbert, De’Broski R. Douglas, Bonnie Zullo, Kelly |
author_sort | Herbert, De’Broski R. |
collection | PubMed |
description | Group 2 innate lymphoid cells (ILC2) have emerged as a major component of type 2 inflammation in mice and humans. ILC2 secrete large amounts of interleukins 5 and 13, which are largely responsible for host protective immunity against helminth parasites because these cytokines induce profound changes in host physiology that include: goblet cell metaplasia, mucus accumulation, smooth muscle hypercontractility, eosinophil and mast cell recruitment, and alternative macrophage activation (M2). This review covers the initial recognition of ILC2 as a distinct cell lineage, the key studies that established their biological importance, particularly in helminth infection, and the new directions that are likely to be the focus of emerging work that further explores this unique cell population in the context of health and disease. |
format | Online Article Text |
id | pubmed-6539149 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-65391492019-06-04 Group 2 Innate Lymphoid Cells (ILC2): Type 2 Immunity and Helminth Immunity Herbert, De’Broski R. Douglas, Bonnie Zullo, Kelly Int J Mol Sci Review Group 2 innate lymphoid cells (ILC2) have emerged as a major component of type 2 inflammation in mice and humans. ILC2 secrete large amounts of interleukins 5 and 13, which are largely responsible for host protective immunity against helminth parasites because these cytokines induce profound changes in host physiology that include: goblet cell metaplasia, mucus accumulation, smooth muscle hypercontractility, eosinophil and mast cell recruitment, and alternative macrophage activation (M2). This review covers the initial recognition of ILC2 as a distinct cell lineage, the key studies that established their biological importance, particularly in helminth infection, and the new directions that are likely to be the focus of emerging work that further explores this unique cell population in the context of health and disease. MDPI 2019-05-08 /pmc/articles/PMC6539149/ /pubmed/31072011 http://dx.doi.org/10.3390/ijms20092276 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Herbert, De’Broski R. Douglas, Bonnie Zullo, Kelly Group 2 Innate Lymphoid Cells (ILC2): Type 2 Immunity and Helminth Immunity |
title | Group 2 Innate Lymphoid Cells (ILC2): Type 2 Immunity and Helminth Immunity |
title_full | Group 2 Innate Lymphoid Cells (ILC2): Type 2 Immunity and Helminth Immunity |
title_fullStr | Group 2 Innate Lymphoid Cells (ILC2): Type 2 Immunity and Helminth Immunity |
title_full_unstemmed | Group 2 Innate Lymphoid Cells (ILC2): Type 2 Immunity and Helminth Immunity |
title_short | Group 2 Innate Lymphoid Cells (ILC2): Type 2 Immunity and Helminth Immunity |
title_sort | group 2 innate lymphoid cells (ilc2): type 2 immunity and helminth immunity |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6539149/ https://www.ncbi.nlm.nih.gov/pubmed/31072011 http://dx.doi.org/10.3390/ijms20092276 |
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