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Heterogeneity of type 2 innate lymphoid cells

More than a decade ago, type 2 innate lymphoid cells (ILC2s) were discovered to be members of a family of innate immune cells consisting of five subsets that form a first line of defence against infections before the recruitment of adaptive immune cells. Initially, ILC2s were implicated in the early...

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Autores principales: Spits, Hergen, Mjösberg, Jenny
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8966870/
https://www.ncbi.nlm.nih.gov/pubmed/35354980
http://dx.doi.org/10.1038/s41577-022-00704-5
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author Spits, Hergen
Mjösberg, Jenny
author_facet Spits, Hergen
Mjösberg, Jenny
author_sort Spits, Hergen
collection PubMed
description More than a decade ago, type 2 innate lymphoid cells (ILC2s) were discovered to be members of a family of innate immune cells consisting of five subsets that form a first line of defence against infections before the recruitment of adaptive immune cells. Initially, ILC2s were implicated in the early immune response to parasitic infections, but it is now clear that ILC2s are highly diverse and have crucial roles in the regulation of tissue homeostasis and repair. ILC2s can also regulate the functions of other type 2 immune cells, including T helper 2 cells, type 2 macrophages and eosinophils. Dysregulation of ILC2s contributes to type 2-mediated pathology in a wide variety of diseases, potentially making ILC2s attractive targets for therapeutic interventions. In this Review, we focus on the spectrum of ILC2 phenotypes that have been described across different tissues and disease states with an emphasis on human ILC2s. We discuss recent insights in ILC2 biology and suggest how this knowledge might be used for novel disease treatments and improved human health.
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spelling pubmed-89668702022-03-31 Heterogeneity of type 2 innate lymphoid cells Spits, Hergen Mjösberg, Jenny Nat Rev Immunol Review Article More than a decade ago, type 2 innate lymphoid cells (ILC2s) were discovered to be members of a family of innate immune cells consisting of five subsets that form a first line of defence against infections before the recruitment of adaptive immune cells. Initially, ILC2s were implicated in the early immune response to parasitic infections, but it is now clear that ILC2s are highly diverse and have crucial roles in the regulation of tissue homeostasis and repair. ILC2s can also regulate the functions of other type 2 immune cells, including T helper 2 cells, type 2 macrophages and eosinophils. Dysregulation of ILC2s contributes to type 2-mediated pathology in a wide variety of diseases, potentially making ILC2s attractive targets for therapeutic interventions. In this Review, we focus on the spectrum of ILC2 phenotypes that have been described across different tissues and disease states with an emphasis on human ILC2s. We discuss recent insights in ILC2 biology and suggest how this knowledge might be used for novel disease treatments and improved human health. Nature Publishing Group UK 2022-03-30 2022 /pmc/articles/PMC8966870/ /pubmed/35354980 http://dx.doi.org/10.1038/s41577-022-00704-5 Text en © Springer Nature Limited 2022 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Review Article
Spits, Hergen
Mjösberg, Jenny
Heterogeneity of type 2 innate lymphoid cells
title Heterogeneity of type 2 innate lymphoid cells
title_full Heterogeneity of type 2 innate lymphoid cells
title_fullStr Heterogeneity of type 2 innate lymphoid cells
title_full_unstemmed Heterogeneity of type 2 innate lymphoid cells
title_short Heterogeneity of type 2 innate lymphoid cells
title_sort heterogeneity of type 2 innate lymphoid cells
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8966870/
https://www.ncbi.nlm.nih.gov/pubmed/35354980
http://dx.doi.org/10.1038/s41577-022-00704-5
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