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Interleukin-18 in Health and Disease

Interleukin (IL)-18 was originally discovered as a factor that enhanced IFN-γ production from anti-CD3-stimulated Th1 cells, especially in the presence of IL-12. Upon stimulation with Ag plus IL-12, naïve T cells develop into IL-18 receptor (IL-18R) expressing Th1 cells, which increase IFN-γ product...

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Detalles Bibliográficos
Autores principales: Yasuda, Koubun, Nakanishi, Kenji, Tsutsui, Hiroko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6387150/
https://www.ncbi.nlm.nih.gov/pubmed/30717382
http://dx.doi.org/10.3390/ijms20030649
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author Yasuda, Koubun
Nakanishi, Kenji
Tsutsui, Hiroko
author_facet Yasuda, Koubun
Nakanishi, Kenji
Tsutsui, Hiroko
author_sort Yasuda, Koubun
collection PubMed
description Interleukin (IL)-18 was originally discovered as a factor that enhanced IFN-γ production from anti-CD3-stimulated Th1 cells, especially in the presence of IL-12. Upon stimulation with Ag plus IL-12, naïve T cells develop into IL-18 receptor (IL-18R) expressing Th1 cells, which increase IFN-γ production in response to IL-18 stimulation. Therefore, IL-12 is a commitment factor that induces the development of Th1 cells. In contrast, IL-18 is a proinflammatory cytokine that facilitates type 1 responses. However, IL-18 without IL-12 but with IL-2, stimulates NK cells, CD4(+) NKT cells, and established Th1 cells, to produce IL-3, IL-9, and IL-13. Furthermore, together with IL-3, IL-18 stimulates mast cells and basophils to produce IL-4, IL-13, and chemical mediators such as histamine. Therefore, IL-18 is a cytokine that stimulates various cell types and has pleiotropic functions. IL-18 is a member of the IL-1 family of cytokines. IL-18 demonstrates a unique function by binding to a specific receptor expressed on various types of cells. In this review article, we will focus on the unique features of IL-18 in health and disease in experimental animals and humans.
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spelling pubmed-63871502019-02-27 Interleukin-18 in Health and Disease Yasuda, Koubun Nakanishi, Kenji Tsutsui, Hiroko Int J Mol Sci Review Interleukin (IL)-18 was originally discovered as a factor that enhanced IFN-γ production from anti-CD3-stimulated Th1 cells, especially in the presence of IL-12. Upon stimulation with Ag plus IL-12, naïve T cells develop into IL-18 receptor (IL-18R) expressing Th1 cells, which increase IFN-γ production in response to IL-18 stimulation. Therefore, IL-12 is a commitment factor that induces the development of Th1 cells. In contrast, IL-18 is a proinflammatory cytokine that facilitates type 1 responses. However, IL-18 without IL-12 but with IL-2, stimulates NK cells, CD4(+) NKT cells, and established Th1 cells, to produce IL-3, IL-9, and IL-13. Furthermore, together with IL-3, IL-18 stimulates mast cells and basophils to produce IL-4, IL-13, and chemical mediators such as histamine. Therefore, IL-18 is a cytokine that stimulates various cell types and has pleiotropic functions. IL-18 is a member of the IL-1 family of cytokines. IL-18 demonstrates a unique function by binding to a specific receptor expressed on various types of cells. In this review article, we will focus on the unique features of IL-18 in health and disease in experimental animals and humans. MDPI 2019-02-02 /pmc/articles/PMC6387150/ /pubmed/30717382 http://dx.doi.org/10.3390/ijms20030649 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
Yasuda, Koubun
Nakanishi, Kenji
Tsutsui, Hiroko
Interleukin-18 in Health and Disease
title Interleukin-18 in Health and Disease
title_full Interleukin-18 in Health and Disease
title_fullStr Interleukin-18 in Health and Disease
title_full_unstemmed Interleukin-18 in Health and Disease
title_short Interleukin-18 in Health and Disease
title_sort interleukin-18 in health and disease
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6387150/
https://www.ncbi.nlm.nih.gov/pubmed/30717382
http://dx.doi.org/10.3390/ijms20030649
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