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癌症免疫疗法中的树突状细胞。

Dendritic cells in cancer immunotherapy.

作者信息

Gunzer M, Grabbe S

机构信息

Department of Dermatology, University of Münster, Germany.

出版信息

Crit Rev Immunol. 2001;21(1-3):133-45.

Abstract

Antigen presentation is a critical regulatory element for the induction of cellular immune responses. Thus, one of the principal current goals of tumor immunotherapy is to control and enhance tumor antigen presentation. In this respect, dendritic cells (DC) are now being widely investigated as immunotherapeutic agents for the treatment of disseminated malignancies. At present, numerous ways to employ DCs for tumor immunotherapy are being tested, ranging from direct in situ expansion and activation of DCs to adoptive transfer of ex vivo generated DCs, and numerous techniques have been designed to optimize DC activation, tumor antigen delivery to DCs, and induction of tumor-specific, as well as helper immune responses, in vivo. However, the results of recent preclinical studies and the diversity of the clinical phase I trials that are currently underway indicate that little is still known about the exact mechanisms by which DCs modulate tumor immunity and pose the concern that premature clinical trials might not yield the desired results and might be harmful to, rather than promote, the concept of DC-based tumor immunotherapy. This review summarizes some of the current approaches to induce tumor immunity by DC-based vaccination and discusses their advantages and concerns.

摘要

抗原呈递是诱导细胞免疫反应的关键调控因素。因此,肿瘤免疫治疗当前的主要目标之一是控制和增强肿瘤抗原呈递。在这方面,树突状细胞(DC)作为治疗播散性恶性肿瘤的免疫治疗药物正受到广泛研究。目前,正在测试多种利用DC进行肿瘤免疫治疗的方法,从直接原位扩增和激活DC到过继转移体外生成的DC,并且已经设计了多种技术来优化DC激活、肿瘤抗原递送至DC以及在体内诱导肿瘤特异性免疫反应和辅助免疫反应。然而,近期临床前研究的结果以及目前正在进行的I期临床试验的多样性表明,对于DC调节肿瘤免疫的确切机制仍知之甚少,这引发了人们的担忧,即过早的临床试验可能无法产生预期结果,可能对基于DC的肿瘤免疫治疗概念有害而非有益。本综述总结了一些当前基于DC疫苗接种诱导肿瘤免疫的方法,并讨论了它们的优点和问题。

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