Department of Dermatology, University Medicine, Johannes Gutenberg-University Mainz, Langenbeckstrasse 1, 55131 Mainz, Germany.
Med Microbiol Immunol. 2012 Nov;201(4):581-92. doi: 10.1007/s00430-012-0261-2. Epub 2012 Sep 16.
Leishmaniasis is one of the most important infectious diseases worldwide; a vaccine is still not available. Infected dendritic cells (DC) are critical for the initiation of protective Th1 immunity against Leishmania major. Phagocytosis of L. major by DC leads to cell activation, IL-12 release and (cross-) presentation of Leishmania antigens by DC. Here, we review the role of Fcγ receptor- and B cell-mediated processes for parasite internalization by DC. In addition, the early events after parasite inoculation that consist of mast cell activation, parasite uptake by skin-resident macrophages (MΦ), followed by neutrophil and monocyte immigration and DC activation are described. All these events contribute significantly to antigen processing in infected DC and influence resulting T cell priming in vivo. A detailed understanding of the role of DC for the development of efficient anti-Leishmania immunity will aid the development of potent anti-parasite drugs and/or vaccines.
利什曼病是全球最重要的传染病之一;目前仍没有可用的疫苗。感染的树突状细胞 (DC) 对于启动针对利什曼原虫的保护性 Th1 免疫至关重要。DC 对利什曼原虫的吞噬作用导致细胞激活、IL-12 释放以及 DC 对利什曼抗原的交叉呈递。在这里,我们回顾了 Fcγ 受体和 B 细胞介导的过程在 DC 摄取寄生虫中的作用。此外,还描述了接种寄生虫后的早期事件,包括肥大细胞激活、皮肤驻留巨噬细胞 (MΦ) 摄取寄生虫,随后中性粒细胞和单核细胞迁移和 DC 激活。所有这些事件都极大地促进了感染 DC 中的抗原加工,并影响体内的 T 细胞启动。深入了解 DC 在产生有效抗利什曼原虫免疫中的作用将有助于开发有效的抗寄生虫药物和/或疫苗。