Urban Elizabeth M, Chapoval Andrei I, Pauza C David
Institute of Human Virology, University of Maryland, School of Medicine, 725 W Lombard Street, Baltimore, MD 21201, USA.
Clin Dev Immunol. 2010;2010:732893. doi: 10.1155/2010/732893. Epub 2010 Apr 13.
T cells develop into two major populations distinguished by their T cell receptor (TCR) chains. Cells with the alphabeta TCR generally express CD4 or CD8 lineage markers and mostly fall into helper or cytotoxic/effector subsets. Cells expressing the alternate gammadelta TCR in humans generally do not express lineage markers, do not require MHC for antigen presentation, and recognize nonpeptidic antigens. We are interested in the dominant Vgamma2Vdelta2+ T cell subset in human peripheral blood and the control of effector function in this population. We review the literature on gammadelta T cell generation and repertoire selection, along with recent work on CD56 expression and defining a cytotoxic/effector lineage within the phosphoantigen-reactive Vgamma2Vdelta2 cells. A unique mechanism for MHC-independent repertoire selection is linked to the control of effector function that is vital to the role for gammadelta T cells in tumor surveillance. Better understanding of these mechanisms will improve our ability to exploit this population for tumor immunotherapy.
T细胞发育成两个主要群体,可通过其T细胞受体(TCR)链加以区分。具有αβTCR的细胞通常表达CD4或CD8谱系标志物,并且大多属于辅助性或细胞毒性/效应子亚群。在人类中表达替代性γδTCR的细胞通常不表达谱系标志物,抗原呈递不需要MHC,并识别非肽类抗原。我们对人类外周血中占主导地位的Vγ2Vδ2 + T细胞亚群以及该群体中效应子功能的调控感兴趣。我们综述了关于γδT细胞生成和谱系选择的文献,以及最近关于CD56表达的研究工作,并在磷酸抗原反应性Vγ2Vδ2细胞中定义了一个细胞毒性/效应子谱系。一种独立于MHC的谱系选择独特机制与效应子功能的调控相关,这对于γδT细胞在肿瘤监视中的作用至关重要。更好地理解这些机制将提高我们利用该群体进行肿瘤免疫治疗的能力。