Rudd Christopher E, Wang Hongyan
Department of Immunology, Faculty of Medicine, Imperial College London, London, UK.
Am J Transplant. 2003 Oct;3(10):1204-10. doi: 10.1046/j.1600-6143.2003.00230.x.
Recent advances have been made in understanding the basis of T-cell signaling with the identification of hematopoeitic-specific adaptor proteins, or molecular scaffolds that facilitate protein complex formation and the integration of signals from the surface of T cells. Their potential relevance as targets in the modulation of transplantation relates to their immune-cell-specific expression and their ability to integrate signals needed for T-cell/APC conjugate formation, cytokine production and the clonal expansion of T cells. While LAT, GADS and SLP-76 are needed for TcR-induced cytokine production, the adaptors ADAP, VAV and SKAP-55 play specialized roles in the regulation of integrin adhesion and conjugation. Given the importance of these functions to the reactivity of T cells to allodeterminants of tissue grafts (GvH), and in the recognition and destruction of leukemic cells (GvL), these adaptors represent a new generation of potential targets in the modulation of transplantation.
随着造血特异性衔接蛋白或分子支架的鉴定,在理解T细胞信号传导基础方面取得了新进展,这些分子支架促进蛋白复合物形成以及整合来自T细胞表面的信号。它们作为移植调节靶点的潜在相关性与其免疫细胞特异性表达以及整合T细胞/抗原呈递细胞(APC)共轭形成、细胞因子产生和T细胞克隆扩增所需信号的能力有关。虽然LAT、GADS和SLP - 76是TcR诱导细胞因子产生所必需的,但衔接蛋白ADAP、VAV和SKAP - 55在整合素粘附和共轭调节中发挥特殊作用。鉴于这些功能对T细胞对组织移植物同种异体决定簇的反应性(移植物抗宿主反应,GvH)以及白血病细胞的识别和破坏(移植物抗白血病作用,GvL)的重要性,这些衔接蛋白代表了移植调节中新一代潜在靶点。