Chikuma Shunsuke
Department of Microbiology and Immunology, Keio University School of Medicine, 35 Shinanomachi, East Lecture Hall 4F, Shinjuku-ku, Tokyo, 160-8582, Japan.
Int J Clin Oncol. 2016 Jun;21(3):448-55. doi: 10.1007/s10147-016-0958-0. Epub 2016 Feb 10.
Successful cancer treatment requires understanding host immune response against tumor cells. PD-1 belongs to the CD28 superfamily of receptors that work as "checkpoints" of immune activation. PD-1 maintains immune self-tolerance to prevent autoimmunity and controls T-cell reaction during infection to prevent excessive tissue damage. Tumor cells that arise from normal tissue acquire mutations that can be targeted by lymphocytes. Accumulating lines of evidence suggest that tumor cells evade host immune attack by expressing physiological PD-1 ligands and stimulating PD-1 on the lymphocytes. Based on this idea, researchers have successfully demonstrated that systemic administration of monoclonal antibodies that inhibit the binding of PD-1 to the ligands reactivated T cells and augmented the anti-cancer immune response. In this review, I summarize the basics of T-cell biology and its regulation by PD-1 and discuss the current understanding and questions about this multifaceted molecule.
成功的癌症治疗需要了解宿主对肿瘤细胞的免疫反应。PD-1属于受体的CD28超家族,其作为免疫激活的“检查点”发挥作用。PD-1维持免疫自我耐受以防止自身免疫,并在感染期间控制T细胞反应以防止过度的组织损伤。源自正常组织的肿瘤细胞获得可被淋巴细胞靶向的突变。越来越多的证据表明,肿瘤细胞通过表达生理性PD-1配体并刺激淋巴细胞上的PD-1来逃避宿主免疫攻击。基于这一想法,研究人员已成功证明,全身施用抑制PD-1与配体结合的单克隆抗体可重新激活T细胞并增强抗癌免疫反应。在这篇综述中,我总结了T细胞生物学的基础知识及其受PD-1调控的情况,并讨论了对这个多面分子的当前理解和相关问题。