von Stebut Esther
Department of Dermatology, Johannes Gutenberg-University Mainz, Mainz, Germany.
Exp Dermatol. 2007 Apr;16(4):340-6. doi: 10.1111/j.1600-0625.2007.00554.x.
Studies in murine experimental Leishmania major infection have helped to understand the requirements for efficient development of T helper (Th)1/cytotoxic T (Tc)1-mediated protection against the parasite. As such they have revealed that Fc gamma receptor (Fc gamma R)I and Fc gamma RIII-mediated uptake of L. major amastigotes by dendritic cells (DC) is an important prerequisite for Th1 development. In addition, DC-derived cytokines contribute to adequate T-cell education. DC-based vaccines may thus provide an important tool for both the development of a prophylactic vaccine against leishmaniasis and - together with leishmanicidal drugs - for eliciting immune-deviating functions towards protective immunity in non-healing leishmaniasis. This review highlights recent advances in the understanding of the role of DC for the induction of Th1/Tc1-predominant immunity against L. major and how this knowledge may translate into clinical approaches.
对小鼠实验性利什曼原虫主要感染的研究有助于了解高效发展辅助性T细胞(Th)1/细胞毒性T细胞(Tc)1介导的针对该寄生虫的保护性免疫的必要条件。因此,这些研究揭示了树突状细胞(DC)通过Fcγ受体(FcγR)I和FcγRIII介导摄取利什曼原虫主要无鞭毛体是Th1细胞发育的重要前提。此外,DC衍生的细胞因子有助于对T细胞进行充分的培养。因此,基于DC的疫苗可能为开发抗利什曼病预防性疫苗以及与杀利什曼原虫药物一起在不愈合的利什曼病中引发偏向保护性免疫的免疫偏离功能提供重要工具。本综述重点介绍了在理解DC在诱导针对利什曼原虫主要感染的以Th1/Tc1为主的免疫中的作用方面的最新进展,以及这些知识如何转化为临床方法。