Department of Medical Oncology, Dana-Farber Cancer Institute, and Department of Medicine, Harvard Medical School, Boston, MA, USA.
Immunol Rev. 2010 May;235(1):172-89. doi: 10.1111/j.0105-2896.2010.00903.x.
The TIM (T cell/transmembrane, immunoglobulin, and mucin) gene family plays a critical role in regulating immune responses, including allergy, asthma, transplant tolerance, autoimmunity, and the response to viral infections. The unique structure of TIM immunoglobulin variable region domains allows highly specific recognition of phosphatidylserine (PtdSer), exposed on the surface of apoptotic cells. TIM-1, TIM-3, and TIM-4 all recognize PtdSer but differ in expression, suggesting that they have distinct functions in regulating immune responses. TIM-1, an important susceptibility gene for asthma and allergy, is preferentially expressed on T-helper 2 (Th2) cells and functions as a potent costimulatory molecule for T-cell activation. TIM-3 is preferentially expressed on Th1 and Tc1 cells, and generates an inhibitory signal resulting in apoptosis of Th1 and Tc1 cells. TIM-3 is also expressed on some dendritic cells and can mediate phagocytosis of apoptotic cells and cross-presentation of antigen. In contrast, TIM-4 is exclusively expressed on antigen-presenting cells, where it mediates phagocytosis of apoptotic cells and plays an important role in maintaining tolerance. TIM molecules thus provide a functional repertoire for recognition of apoptotic cells, which determines whether apoptotic cell recognition leads to immune activation or tolerance, depending on the TIM molecule engaged and the cell type on which it is expressed.
TIM(T 细胞/跨膜、免疫球蛋白和粘蛋白)基因家族在调节免疫反应中起着关键作用,包括过敏、哮喘、移植耐受、自身免疫和对病毒感染的反应。TIM 免疫球蛋白可变区结构域的独特结构允许对凋亡细胞表面暴露的磷脂酰丝氨酸(PtdSer)进行高度特异性识别。TIM-1、TIM-3 和 TIM-4 都识别 PtdSer,但表达不同,表明它们在调节免疫反应方面具有不同的功能。TIM-1 是哮喘和过敏的重要易感基因,优先表达在 T 辅助 2(Th2)细胞上,并作为 T 细胞激活的有效共刺激分子发挥作用。TIM-3 优先表达在 Th1 和 Tc1 细胞上,并产生抑制信号,导致 Th1 和 Tc1 细胞凋亡。TIM-3 也表达在一些树突状细胞上,并能介导凋亡细胞的吞噬作用和抗原的交叉呈递。相比之下,TIM-4 仅表达在抗原呈递细胞上,在那里它介导凋亡细胞的吞噬作用,并在维持耐受中发挥重要作用。TIM 分子因此为识别凋亡细胞提供了功能组合,这取决于参与的 TIM 分子和表达该分子的细胞类型,决定了凋亡细胞识别是否导致免疫激活或耐受。