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Resident-Memory T Cells in Tissue-Restricted Immune Responses: For Better or Worse?

Tissue-resident-memory CD8+ T cells (T(RM)) have been described as a non-circulating memory T cell subset that persists at sites of previous infection. While T(RM) in all non-lymphoid organs probably share a core signature differentiation pathway, certain aspects of their maintenance and effector fu...

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Detalles Bibliográficos
Autores principales: Steinbach, Karin, Vincenti, Ilena, Merkler, Doron
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6284001/
https://www.ncbi.nlm.nih.gov/pubmed/30555489
http://dx.doi.org/10.3389/fimmu.2018.02827
Descripción
Sumario:Tissue-resident-memory CD8+ T cells (T(RM)) have been described as a non-circulating memory T cell subset that persists at sites of previous infection. While T(RM) in all non-lymphoid organs probably share a core signature differentiation pathway, certain aspects of their maintenance and effector functions may vary. It is well-established that T(RM) provide long-lived protective immunity through immediate effector function and accelerated recruitment of circulating immune cells. Besides immune defense against pathogens, other immunological roles of T(RM) are less well-studied. Likewise, evidence of a putative detrimental role of T(RM) for inflammatory diseases is only beginning to emerge. In this review, we discuss the protective and harmful role of T(RM) in organ-specific immunity and immunopathology as well as prospective implications for immunomodulatory therapy.