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A new player on the psoriasis block: IL-17A- and IL-22-producing innate lymphoid cells

Innate lymphoid cells (ILCs) are a recently discovered family of innate immune cells belonging to the lymphoid lineage, yet lacking antigen-specific receptors. ILCs were first identified in the intestinal tract, where they contribute to epithelial barrier integrity and host responses to commensal mi...

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Detalles Bibliográficos
Autores principales: Ward, Nicole L., Umetsu, Dale T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4134095/
https://www.ncbi.nlm.nih.gov/pubmed/25120146
http://dx.doi.org/10.1038/jid.2014.216
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author Ward, Nicole L.
Umetsu, Dale T.
author_facet Ward, Nicole L.
Umetsu, Dale T.
author_sort Ward, Nicole L.
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description Innate lymphoid cells (ILCs) are a recently discovered family of innate immune cells belonging to the lymphoid lineage, yet lacking antigen-specific receptors. ILCs were first identified in the intestinal tract, where they contribute to epithelial barrier integrity and host responses to commensal microbes. Teunissen et al. in the current issue and Villanova et al. (JID, 134, 984-99) now suggest an important role for type 3 ILCs (ILC3s) in the skin, particularly in psoriasis. Both groups found an increased frequency of IL-22- and/or IL-17A-producing ILCs in psoriatic skin and blood. These cells are activated in response to IL-1β and IL-23, correlate with disease severity, and are decreased following anti-TNFα treatment. The presence of a novel ILC population in psoriatic skin, one that responds to biologic therapeutics, suggests that dysregulation of ILCs is a contributing factor to psoriasis pathogenesis.
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spelling pubmed-41340952015-03-01 A new player on the psoriasis block: IL-17A- and IL-22-producing innate lymphoid cells Ward, Nicole L. Umetsu, Dale T. J Invest Dermatol Article Innate lymphoid cells (ILCs) are a recently discovered family of innate immune cells belonging to the lymphoid lineage, yet lacking antigen-specific receptors. ILCs were first identified in the intestinal tract, where they contribute to epithelial barrier integrity and host responses to commensal microbes. Teunissen et al. in the current issue and Villanova et al. (JID, 134, 984-99) now suggest an important role for type 3 ILCs (ILC3s) in the skin, particularly in psoriasis. Both groups found an increased frequency of IL-22- and/or IL-17A-producing ILCs in psoriatic skin and blood. These cells are activated in response to IL-1β and IL-23, correlate with disease severity, and are decreased following anti-TNFα treatment. The presence of a novel ILC population in psoriatic skin, one that responds to biologic therapeutics, suggests that dysregulation of ILCs is a contributing factor to psoriasis pathogenesis. 2014-09 /pmc/articles/PMC4134095/ /pubmed/25120146 http://dx.doi.org/10.1038/jid.2014.216 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Ward, Nicole L.
Umetsu, Dale T.
A new player on the psoriasis block: IL-17A- and IL-22-producing innate lymphoid cells
title A new player on the psoriasis block: IL-17A- and IL-22-producing innate lymphoid cells
title_full A new player on the psoriasis block: IL-17A- and IL-22-producing innate lymphoid cells
title_fullStr A new player on the psoriasis block: IL-17A- and IL-22-producing innate lymphoid cells
title_full_unstemmed A new player on the psoriasis block: IL-17A- and IL-22-producing innate lymphoid cells
title_short A new player on the psoriasis block: IL-17A- and IL-22-producing innate lymphoid cells
title_sort new player on the psoriasis block: il-17a- and il-22-producing innate lymphoid cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4134095/
https://www.ncbi.nlm.nih.gov/pubmed/25120146
http://dx.doi.org/10.1038/jid.2014.216
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