Crittenden Marka R, Thanarajasingam Uma, Vile Richard G, Gough Michael J
Molecular Medicine Program, Mayo Clinic, Rochester, MN, USA.
Immunology. 2005 Jan;114(1):11-22. doi: 10.1111/j.1365-2567.2004.02001.x.
Summary Diverse immunotherapy approaches have achieved success in controlling individual aspects of immune responses in animal models. Transfer of such immunotherapies to clinical trials has obtained some success in patients, with clinical responses observed or effective antigen specific immune responses achieved, but has had limited impact on patient survival. Key elements required to generate de novo cell-mediated antitumour immune responses in vivo include recruitment of antigen-presenting cells to the tumour site, loading these cells with antigen, and their migration and maturation to full antigen-presenting function. In addition, it is essential for antigen-specific T cells to locate the tumour to mediate cytotoxicity, emphasizing the need for local inflammation to target effector cell recruitment. We review those therapies that involve the tumour site as a target and source of antigen for the initiation of immune responses, and discuss strategies to generate and co-ordinate an optimal cell-mediated immune response to control tumours locally.
多种免疫疗法已在动物模型中成功控制免疫反应的各个方面。将此类免疫疗法应用于临床试验已在患者中取得了一些成功,观察到了临床反应或实现了有效的抗原特异性免疫反应,但对患者生存率的影响有限。在体内产生全新的细胞介导的抗肿瘤免疫反应所需的关键要素包括将抗原呈递细胞募集到肿瘤部位,使这些细胞负载抗原,以及它们迁移并成熟至具有完整的抗原呈递功能。此外,抗原特异性T细胞必须定位到肿瘤部位以介导细胞毒性,这强调了需要局部炎症来靶向效应细胞募集。我们综述了那些将肿瘤部位作为免疫反应启动的靶点和抗原来源的疗法,并讨论了产生和协调最佳细胞介导免疫反应以局部控制肿瘤的策略。