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Current Developments in the Immunology of Psoriasis

Psoriasis is a frequent inflammatory skin disease. Fundamental research on the pathogenesis of psoriasis has substantially increased our understanding of skin immunology, which has helped to introduce innovative and highly effective therapies. Psoriasis is a largely T lymphocyte-mediated disease in...

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Autores principales: Grän, Franziska, Kerstan, Andreas, Serfling, Edgar, Goebeler, Matthias, Muhammad, Khalid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: YJBM 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7087066/
https://www.ncbi.nlm.nih.gov/pubmed/32226340
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author Grän, Franziska
Kerstan, Andreas
Serfling, Edgar
Goebeler, Matthias
Muhammad, Khalid
author_facet Grän, Franziska
Kerstan, Andreas
Serfling, Edgar
Goebeler, Matthias
Muhammad, Khalid
author_sort Grän, Franziska
collection PubMed
description Psoriasis is a frequent inflammatory skin disease. Fundamental research on the pathogenesis of psoriasis has substantially increased our understanding of skin immunology, which has helped to introduce innovative and highly effective therapies. Psoriasis is a largely T lymphocyte-mediated disease in which activation of innate immune cells and pathogenic T cells result in skin inflammation and hyperproliferation of keratinocytes. B cells have thus far largely been neglected regarding their role for the pathogenesis of psoriasis. However, recent data shed light on their role in inflammatory skin diseases. Interestingly, interleukin (IL)-10-producing regulatory B cells have been assumed to ameliorate psoriasis. In this review, we will discuss the development of disease, pathogenicity, and current developments in therapeutic options. We describe different roles of T cells, B cells, and cytokines for the immunopathology and disease course of psoriasis.
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spelling pubmed-70870662020-03-27 Current Developments in the Immunology of Psoriasis Grän, Franziska Kerstan, Andreas Serfling, Edgar Goebeler, Matthias Muhammad, Khalid Yale J Biol Med Review Psoriasis is a frequent inflammatory skin disease. Fundamental research on the pathogenesis of psoriasis has substantially increased our understanding of skin immunology, which has helped to introduce innovative and highly effective therapies. Psoriasis is a largely T lymphocyte-mediated disease in which activation of innate immune cells and pathogenic T cells result in skin inflammation and hyperproliferation of keratinocytes. B cells have thus far largely been neglected regarding their role for the pathogenesis of psoriasis. However, recent data shed light on their role in inflammatory skin diseases. Interestingly, interleukin (IL)-10-producing regulatory B cells have been assumed to ameliorate psoriasis. In this review, we will discuss the development of disease, pathogenicity, and current developments in therapeutic options. We describe different roles of T cells, B cells, and cytokines for the immunopathology and disease course of psoriasis. YJBM 2020-03-27 /pmc/articles/PMC7087066/ /pubmed/32226340 Text en Copyright ©2020, Yale Journal of Biology and Medicine https://creativecommons.org/licenses/by-nc/4.0/ This is an open access article distributed under the terms of the Creative Commons CC BY-NC license, which permits use, distribution, and reproduction in any medium, provided the original work is properly cited. You may not use the material for commercial purposes.
spellingShingle Review
Grän, Franziska
Kerstan, Andreas
Serfling, Edgar
Goebeler, Matthias
Muhammad, Khalid
Current Developments in the Immunology of Psoriasis
title Current Developments in the Immunology of Psoriasis
title_full Current Developments in the Immunology of Psoriasis
title_fullStr Current Developments in the Immunology of Psoriasis
title_full_unstemmed Current Developments in the Immunology of Psoriasis
title_short Current Developments in the Immunology of Psoriasis
title_sort current developments in the immunology of psoriasis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7087066/
https://www.ncbi.nlm.nih.gov/pubmed/32226340
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