Grünebach Frank, Müller Martin R, Brossart Peter
Department of Internal Medicine II, Division of Hematology, Immunology, and Oncology, University of Tübingen, Otfried-Müller-Str. 10, 72076, Tübingen, Germany.
Cancer Immunol Immunother. 2005 Jun;54(6):517-25. doi: 10.1007/s00262-004-0605-x. Epub 2005 Jan 27.
Dendritic cells (DCs) are the most powerful antigen-presenting cells that induce and maintain primary immune responses in vitro and in vivo. The development of protocols for the ex vivo generation of DCs provided a rationale for designing and developing DC-based vaccination studies for the treatment of infectious and malignant diseases. Recently, it was shown that DCs transfected with ribonucleic acid (RNA) coding for a tumour-associated antigen or whole tumour RNA are able to induce potent antigen and tumour-specific T-cell responses directed against multiple epitopes. The first RNA-transfected-DC-based clinical studies have shown that this form of vaccination is feasible and safe. In some cases, clinical responses were observed, but the preliminary data require further extensive investigations that should address the technical and biological problems of manipulating human DCs, as well as the development of standardised protocols and definitions of clinical settings.
树突状细胞(DCs)是最强大的抗原呈递细胞,可在体内外诱导并维持初次免疫反应。体外生成DCs的方案的发展为设计和开展基于DC的疫苗接种研究以治疗感染性疾病和恶性疾病提供了理论依据。最近研究表明,用编码肿瘤相关抗原的核糖核酸(RNA)或完整肿瘤RNA转染的DCs能够诱导针对多个表位的强效抗原及肿瘤特异性T细胞反应。首批基于RNA转染DCs的临床研究表明,这种疫苗接种形式是可行且安全的。在某些情况下,观察到了临床反应,但初步数据需要进一步广泛研究,这些研究应解决操控人类DCs的技术和生物学问题,以及标准化方案的制定和临床环境的定义。