Fry T J, Mackall C L
Pediatric Oncology Branch, National Cancer Institute, National Institutes of Health, Building 10, Room 13N240, 10 Center Drive, MSC 1928, Bethesda, MD 20892-1928, USA.
Trends Immunol. 2001 Oct;22(10):564-71. doi: 10.1016/s1471-4906(01)02028-2.
Recent evidence has implicated interleukin-7 (IL-7) as a master regulator of T-cell homeostasis, based upon its essential role in the homeostatic expansion of naive T-cell populations in response to low-affinity antigens (Ags) and its capacity to enhance dramatically the expansion of peripheral T-cell populations in response to high-affinity Ags. Furthermore, T-cell-depleted humans have a unique inverse relationship between the peripheral CD4(+) T-cell count and the level of circulating IL-7. Together, these data suggest that increased amounts of IL-7 become available following T-cell depletion, thus, enhancing the high- and low-affinity Ag-driven expansion of the population of residual, mature T cells and boosting thymic regenerative capacity, as a means to restore T-cell homeostasis.
最近的证据表明,白细胞介素-7(IL-7)是T细胞稳态的主要调节因子,这是基于其在低亲和力抗原(Ags)作用下幼稚T细胞群体稳态扩增中的关键作用,以及其显著增强外周T细胞群体对高亲和力Ags反应性扩增的能力。此外,T细胞耗竭的人类外周CD4(+) T细胞计数与循环IL-7水平之间存在独特的负相关关系。这些数据共同表明,T细胞耗竭后IL-7的量会增加,从而增强残余成熟T细胞群体对高亲和力和低亲和力Ags驱动的扩增,并提高胸腺再生能力,以此作为恢复T细胞稳态的一种手段。