Kaech Susan M, Tan Joyce T, Wherry E John, Konieczny Bogumila T, Surh Charles D, Ahmed Rafi
Emory Vaccine Center and Department of Microbiology and Immunology, Emory University School of Medicine, 1510 Clifton Road, Atlanta, Georgia 30322, USA.
Nat Immunol. 2003 Dec;4(12):1191-8. doi: 10.1038/ni1009. Epub 2003 Nov 16.
A major unanswered question is what distinguishes the majority of activated CD8 T cells that die after an acute viral infection from the small fraction (5-10%) that survive to become long-lived memory cells. In this study we show that increased expression of the interleukin 7 receptor alpha-chain (IL-7Ralpha) identifies the effector CD8 T cells that will differentiate into memory cells. IL-7R(hi) effector cells contained increased amounts of antiapoptotic molecules, and adoptive transfer of IL-7R(hi) and IL-7R(lo) effector cells showed that IL-7R(hi) cells preferentially gave rise to memory cells that could persist and confer protective immunity. Thus, selective expression of IL-7R identifies memory cell precursors, and this marker may be useful in predicting the number of memory T cells generated after infection or immunization.
一个主要的未解决问题是,在急性病毒感染后死亡的大多数活化CD8 T细胞与存活下来成为长寿记忆细胞的一小部分(5%-10%)之间有何区别。在本研究中,我们表明白细胞介素7受体α链(IL-7Rα)表达的增加可识别将分化为记忆细胞的效应CD8 T细胞。IL-7R(hi)效应细胞含有更多的抗凋亡分子,对IL-7R(hi)和IL-7R(lo)效应细胞进行过继转移表明,IL-7R(hi)细胞优先产生能够持续存在并赋予保护性免疫的记忆细胞。因此,IL-7R的选择性表达可识别记忆细胞前体,并且该标志物可能有助于预测感染或免疫后产生的记忆T细胞数量。