So Takanori, Lee Seung-Woo, Croft Michael
Division of Molecular Immunology, La Jolla Institute for Allergy and Immunology, 9420 Athena Circle, La Jolla, CA 92037, USA.
Cytokine Growth Factor Rev. 2008 Jun-Aug;19(3-4):253-62. doi: 10.1016/j.cytogfr.2008.04.003. Epub 2008 May 27.
The TNFR family members OX40 (CD134) and 4-1BB (CD137) have been found to play major roles as costimulatory receptors for both CD4 and CD8 T cells. In particular, in many situations, they can control proliferation, survival, and cytokine production, and hence are thought to dictate accumulation of protective T cells during anti-viral and anti-tumor responses and pathogenic T cells during autoimmune reactions. As opposed to simply controlling the activity of naïve, effector, and memory T cells, recent data have suggested that both molecules are also instrumental in controlling the generation and activity of so-called regulatory or suppressor T cells (Treg), perhaps in both positive and negative manners. Part of the action on Treg might function to further promote protective or pathogenic T cells, but alternate activities of OX40 and 4-1BB on Treg are also being described that suggest that there might be control by these molecules at multiple levels that will alter the biological outcome when these receptors are ligated. This review specifically focuses on recent studies of regulatory T cells, and regulatory or suppressive activity, that are modulated by OX40 or 4-1BB.
肿瘤坏死因子受体(TNFR)家族成员OX40(CD134)和4-1BB(CD137)已被发现作为CD4和CD8 T细胞的共刺激受体发挥主要作用。特别是,在许多情况下,它们可以控制增殖、存活和细胞因子产生,因此被认为在抗病毒和抗肿瘤反应中决定保护性T细胞的积累,在自身免疫反应中决定致病性T细胞的积累。与简单地控制初始T细胞、效应T细胞和记忆T细胞的活性不同,最近的数据表明这两种分子在控制所谓的调节性或抑制性T细胞(Treg)的产生和活性方面也发挥着作用,可能是以正向和负向两种方式。对Treg的部分作用可能是进一步促进保护性或致病性T细胞,但也有关于OX40和4-1BB对Treg的其他活性的描述,这表明这些分子可能在多个水平上进行调控,当这些受体被激活时会改变生物学结果。本综述特别关注受OX40或4-1BB调节的调节性T细胞以及调节或抑制活性的最新研究。