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Analysis of expression and function of the costimulatory molecule 4-1BB in alloimmune responses.
Tan, J T; Ha, J; Cho, H R; Tucker-Burden, C; Hendrix, R C; Mittler, R S; Pearson, T C; Larsen, C P.
Afiliación
  • Tan JT; The Carlos and Marguerite Mason Transplantation Biology Research Center and Department of Surgery, Emory University School of Medicine, Atlanta, GA 30322, USA.
Transplantation ; 70(1): 175-83, 2000 Jul 15.
Article en En | MEDLINE | ID: mdl-10919597
BACKGROUND: 4-1BB (CD137) is a T cell costimulatory molecule that promotes T cell activation. In this study, we investigated the role of 4-1BB costimulation in allogeneic T cell responses. METHODS: Vascularized heart transplantation, allogeneic mixed leukocyte reaction (MLR), and graft versus host disease models were used to examine 4-1BB and 4-1BBL expression. In addition, agonistic anti-4-1BB antibodies were used in MLR to functionally analyze T cell responses. RESULTS: Using a heart transplant model, we found that 4-1BB and 4-1BBL transcripts were both expressed in rejecting cardiac grafts. In the allogeneic MLR, 4-1BB was expressed on both activated CD4 and CD8 T cells and 4-1BB was expressed on T cells after multiple cell divisions in vivo. Functionally, 4-1BB was a potent stimulator of proliferation, cytokine secretion, and CD25 expression by CD8 T cells, but 4-1BB signals had a weak effect on the proliferation of CD4 T cells. Because 4-1BB promoted the secretion of IL-2 and the expression of CD25 on CD8 T cells, we investigated whether IL-2 was the only factor whereby 4-1BB signals induced CD8 T cell proliferation. Although IL-2 was required for optimal CD8 T cell proliferation, 4-1BB also costimulated CD8 T cell proliferation independently of IL-2. CONCLUSIONS: This study demonstrates that 4-1BB is expressed on activated, maximally divided T cells and shows that 4-1BB promotes CD8 T cell proliferation by enhancing signals through the IL-2 receptor and by other mechanisms independent of the IL-2 pathway.
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Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Linfocitos T / Receptores de Factor de Crecimiento Nervioso / Receptores del Factor de Necrosis Tumoral Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Transplantation Año: 2000 Tipo del documento: Article País de afiliación: Estados Unidos
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Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Linfocitos T / Receptores de Factor de Crecimiento Nervioso / Receptores del Factor de Necrosis Tumoral Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Transplantation Año: 2000 Tipo del documento: Article País de afiliación: Estados Unidos