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CD49a Regulates Cutaneous Resident Memory CD8+ T Cell Persistence and Response.
Bromley, Shannon K; Akbaba, Hasan; Mani, Vinidhra; Mora-Buch, Rut; Chasse, Alexandra Y; Sama, Andrea; Luster, Andrew D.
Afiliación
  • Bromley SK; Center for Immunology and Inflammatory Diseases, Division of Rheumatology, Allergy and Immunology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA. Electronic address: sbromley@mgh.harvard.edu.
  • Akbaba H; Center for Immunology and Inflammatory Diseases, Division of Rheumatology, Allergy and Immunology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA; Department of Pharmaceutical Biotechnology Faculty of Pharmacy, Ege University, 35100, Bornova, Izmir, Turkey.
  • Mani V; Center for Immunology and Inflammatory Diseases, Division of Rheumatology, Allergy and Immunology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA; Immunology Graduate Program, Harvard Medical School, Boston, MA, USA.
  • Mora-Buch R; Center for Immunology and Inflammatory Diseases, Division of Rheumatology, Allergy and Immunology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
  • Chasse AY; Center for Immunology and Inflammatory Diseases, Division of Rheumatology, Allergy and Immunology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
  • Sama A; Center for Immunology and Inflammatory Diseases, Division of Rheumatology, Allergy and Immunology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
  • Luster AD; Center for Immunology and Inflammatory Diseases, Division of Rheumatology, Allergy and Immunology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
Cell Rep ; 32(9): 108085, 2020 09 01.
Article en En | MEDLINE | ID: mdl-32877667
ABSTRACT
CD8+ tissue-resident memorycells (TRM) persist at sites of previous infection, where they provide rapid local protection against pathogen challenge. CD8+ TRM expressing the α1 chain (CD49a) of integrin VLA-1 have been identified within sites of resolved skin infection and in vitiligo lesions. We demonstrate that CD49a is expressed early following T cell activation in vivo, and TGF-ß and IL-12 induce CD49a expression by CD8+ T cells in vitro. Despite this rapid expression, CD49a is not required for the generation of a primary CD8+ T cell response to cutaneous herpes simplex virus (HSV) infection, migration of CD8+ T cells across the epidermal basement membrane, or positioning of TRM within basal epidermis. Rather, CD49a supports CD8+ TRM persistence within skin, regulates epidermal CD8+ TRM dendritic extensions, and increases the frequency of IFN-γ+ CD8+ TRM following local antigen challenge. Our results suggest that CD49a promotes optimal cutaneous CD8+ TRM-mediated immunity.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Linfocitos T / Linfocitos T CD8-positivos / Integrina alfa1 Límite: Animals Idioma: En Revista: Cell Rep Año: 2020 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Linfocitos T / Linfocitos T CD8-positivos / Integrina alfa1 Límite: Animals Idioma: En Revista: Cell Rep Año: 2020 Tipo del documento: Article