Salek-Ardakani Shahram, Croft Michael
Division of Molecular Immunology, La Jolla Institute for Allergy and Immunology, San Diego, CA 92121, USA.
Vaccine. 2006 Feb 13;24(7):872-83. doi: 10.1016/j.vaccine.2005.07.108. Epub 2005 Sep 7.
CD4 memory T cells play a critical role in protection against repeated exposure to infectious agents such as viruses, bacteria, and helminth parasites, yet can also contribute to the aberrant immune responses associated with autoimmune and allergic reactions. Understanding the mechanisms that control effective memory responses has important ramifications for vaccine design and in the management of adverse immune reactions. Recent advances in studies of T cell memory have implicated the tumor-necrosis-factor receptor (TNFR) family member, OX40 (CD134), as a key co-stimulatory molecule involved in the regulation of CD4 memory T cells. In this review we discuss these new developments in the context of past research and current models for the generation, persistence, and re-activation of memory T cells.
CD4记忆T细胞在抵御病毒、细菌和蠕虫寄生虫等感染因子的反复感染中发挥着关键作用,但也可能导致与自身免疫和过敏反应相关的异常免疫反应。了解控制有效记忆反应的机制对疫苗设计和不良免疫反应的管理具有重要意义。T细胞记忆研究的最新进展表明,肿瘤坏死因子受体(TNFR)家族成员OX40(CD134)是参与调节CD4记忆T细胞的关键共刺激分子。在这篇综述中,我们将在过去研究以及记忆T细胞产生、维持和重新激活的当前模型的背景下讨论这些新进展。