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Effector T Helper Cell Subsets in Inflammatory Bowel Diseases

The gastrointestinal tract is a site of high immune challenge, as it must maintain a delicate balance between tolerating luminal contents and generating an immune response toward pathogens. CD4(+) T cells are key in mediating the host protective and homeostatic responses. Yet, CD4(+) T cells are als...

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Detalles Bibliográficos
Autores principales: Imam, Tanbeena, Park, Sungtae, Kaplan, Mark H., Olson, Matthew R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5992276/
https://www.ncbi.nlm.nih.gov/pubmed/29910812
http://dx.doi.org/10.3389/fimmu.2018.01212
Descripción
Sumario:The gastrointestinal tract is a site of high immune challenge, as it must maintain a delicate balance between tolerating luminal contents and generating an immune response toward pathogens. CD4(+) T cells are key in mediating the host protective and homeostatic responses. Yet, CD4(+) T cells are also known to be the main drivers of inflammatory bowel disease (IBD) when this balance is perturbed. Many subsets of CD4(+) T cells have been identified as players in perpetuating chronic intestinal inflammation. Over the last few decades, understanding of how each subset of Th cells plays a role has dramatically increased. Simultaneously, this has allowed development of therapeutic innovation targeting specific molecules rather than broad immunosuppressive agents. Here, we review the emerging evidence of how each subset functions in promoting and sustaining the chronic inflammation that characterizes IBD.