Surh Charles D, Boyman Onur, Purton Jared F, Sprent Jonathan
The Scripps Research Institute, La Jolla, CA 92037, USA.
Immunol Rev. 2006 Jun;211:154-63. doi: 10.1111/j.0105-2896.2006.00401.x.
The pool of memory T cells is regulated by homeostatic mechanisms to persist for prolonged periods at a relatively steady overall size. Recent work has shown that two members of the common gamma chain (gammac) family of cytokines, interleukin-7 (IL-7) and IL-15, govern homeostasis of memory T cells. These two cytokines work in conjunction to support memory T-cell survival and intermittent background proliferation. Normal animals contain significant numbers of spontaneously arising memory-phenotype (MP) cells, though whether these cells are representative of true antigen-specific memory T cells is unclear. Nevertheless, it appears that the two types of memory cells do not display identical homeostatic requirements. For antigen-specific memory CD8+ T cells, IL-7 is primarily important for survival while IL-15 is crucial for their background proliferation. For memory CD4+ T cells, IL-7 has an important role, whereas the influence of IL-15 is still unclear.
记忆性T细胞库受稳态机制调控,以相对稳定的总体规模长期维持。最近的研究表明,细胞因子共同γ链(γc)家族的两个成员,即白细胞介素-7(IL-7)和IL-15,控制着记忆性T细胞的稳态。这两种细胞因子协同作用,以支持记忆性T细胞的存活和间歇性的背景增殖。正常动物含有大量自发产生的记忆表型(MP)细胞,不过这些细胞是否代表真正的抗原特异性记忆性T细胞尚不清楚。然而,这两种类型的记忆细胞似乎并不表现出相同的稳态需求。对于抗原特异性记忆性CD8+T细胞,IL-7对其存活至关重要,而IL-15对其背景增殖至关重要。对于记忆性CD4+T细胞,IL-7发挥重要作用,而IL-15的影响仍不清楚。