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γδ T cells develop, respond and survive - with a little help from CD27.
Born, Willi K; O'Brien, Rebecca L.
Afiliação
  • Born WK; Integrated Department of Immunology, National Jewish Health and University of Colorado Health Sciences Center, Denver, CO 80206, USA. bornw@njhealth.org
Eur J Immunol ; 41(1): 26-8, 2011 Jan.
Article em En | MEDLINE | ID: mdl-21182073
Although the TNF receptor family member CD27 has been known for some time, its functional role as a coreceptor on T and B cells remains poorly understood. Recent reports have shown that CD27 and its ligand CD70 play a critical role in the development and function of γδ T cells in mice. In this issue of the European Journal of Immunology, a study now extends these findings to the Vγ9Vδ2(+) subset of human γδ T cells. This subset, whose responses are readily elicited by phosphoantigens, plays an important role in anti-tumor immune responses. This study shows that most Vγ9Vδ2(+) cells express CD27, and signaling via the CD27-CD70 axis is needed for their survival, proliferation and cytokine secretion. Moreover, CD27 functions as a coreceptor, which promotes, in conjunction with TCR-mediated signals, expansion of Th1-biased Vγ9Vδ2(+) cells. This new information underscores the significance of CD27 in γδ T-cell functional differentiation, and is likely to facilitate the development of γδ T-cell-based clinical immunotherapy.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Subpopulações de Linfócitos T / Receptores de Antígenos de Linfócitos T gama-delta / Membro 7 da Superfamília de Receptores de Fatores de Necrose Tumoral Limite: Animals / Humans Idioma: En Ano de publicação: 2011 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Subpopulações de Linfócitos T / Receptores de Antígenos de Linfócitos T gama-delta / Membro 7 da Superfamília de Receptores de Fatores de Necrose Tumoral Limite: Animals / Humans Idioma: En Ano de publicação: 2011 Tipo de documento: Article