La Jolla Institute for Allergy and Immunology, California 92037, USA.
Annu Rev Immunol. 2010;28:57-78. doi: 10.1146/annurev-immunol-030409-101243.
TNFR/TNF superfamily members can control diverse aspects of immune function. Research over the past 10 years has shown that one of the most important and prominent interactions in this family is that between OX40 (CD134) and its partner OX40L (CD252). These molecules strongly regulate conventional CD4 and CD8 T cells, and more recent data are highlighting their ability to modulate NKT cell and NK cell function as well as to mediate cross-talk with professional antigen-presenting cells and diverse cell types such as mast cells, smooth muscle cells, and endothelial cells. Additionally, OX40-OX40L interactions alter the differentiation and activity of regulatory T cells. Blocking OX40L has produced strong therapeutic effects in multiple animal models of autoimmune and inflammatory disease, and, in line with a prospective clinical future, reagents that stimulate OX40 signaling are showing promise as adjuvants for vaccination as well as for treatment of cancer.
肿瘤坏死因子受体/肿瘤坏死因子超家族成员可以控制免疫功能的多个方面。过去 10 年的研究表明,该家族中最重要和突出的相互作用之一是 OX40(CD134)与其配体 OX40L(CD252)之间的相互作用。这些分子强烈调节常规 CD4 和 CD8 T 细胞,最近的数据强调了它们调节 NKT 细胞和 NK 细胞功能以及与专业抗原呈递细胞和多种细胞类型(如肥大细胞、平滑肌细胞和内皮细胞)进行交叉对话的能力。此外,OX40-OX40L 相互作用改变了调节性 T 细胞的分化和活性。阻断 OX40L 在多种自身免疫和炎症性疾病的动物模型中产生了强烈的治疗效果,并且与预期的临床前景一致,刺激 OX40 信号的试剂作为佐剂在疫苗接种以及癌症治疗方面显示出前景。