Suppr超能文献

感染硕大利什曼原虫的免疫小鼠体内的树突状细胞含有持续性寄生虫,并介导抗原特异性T细胞免疫反应。

Dendritic cells in Leishmania major-immune mice harbor persistent parasites and mediate an antigen-specific T cell immune response.

作者信息

Moll H, Flohé S, Röllinghoff M

机构信息

Institute of Clinical Microbiology and Immunology, University of Erlangen-Nürnberg, Germany.

出版信息

Eur J Immunol. 1995 Mar;25(3):693-9. doi: 10.1002/eji.1830250310.

Abstract

Upon infection with Leishmania major, a cause of human cutaneous leishmaniasis, mice of resistant strains are able to control the infection, with lesions resolving spontaneously. A long-lasting cell-mediated immunity protects them from reinfection. Nevertheless, small numbers of viable parasites persist in the lymph nodes of these mice. We have recently documented that, in addition to macrophages, epidermal Langerhans cells can ingest L. major. Furthermore, Langerhans cells have the unique ability to transport viable parasites from the infected skin to the draining lymph node for presentation to antigen-specific T cells and initiation of the cellular immune response. During migration, Langerhans cells develop into dendritic cells. In the present study, we analyzed whether dendritic cells support the persistence of parasites in immune hosts. Immunohistological studies and assays in vitro showed that in the lymph nodes of mice that have recovered from infection with L. major, both macrophages and dendritic cells harbor viable parasites. However, only dendritic cells were able to induce a vigorous T-cell immune response to L. major in vitro in the absence of exogenous antigen. Tracking experiments conducted in vivo suggested that the infected dendritic cells in the lymph nodes are derived from Langerhans cells that have emigrated from the skin. The data demonstrate that L. major-infected dendritic cells and macrophages in lymph nodes of immune animals represent long-term host cells, but only dendritic cells have the ability to present endogenous parasite antigen to T cells. Long-term infected dendritic cells may thus allow the sustained stimulation of a population of parasite-specific T cells, protecting the mice from reinfection. Our results favor the hypothesis that the persistence of antigen supports the maintenance of T cell memory and that dendritic cells are critically involved in this process.

摘要

感染引起人类皮肤利什曼病的硕大利什曼原虫后,抗性品系的小鼠能够控制感染,损伤会自发消退。持久的细胞介导免疫保护它们免受再次感染。然而,这些小鼠的淋巴结中仍有少量活的寄生虫持续存在。我们最近记录到,除巨噬细胞外,表皮朗格汉斯细胞也能摄取硕大利什曼原虫。此外,朗格汉斯细胞具有将活的寄生虫从感染的皮肤转运至引流淋巴结以呈递给抗原特异性T细胞并启动细胞免疫反应的独特能力。在迁移过程中,朗格汉斯细胞会发育成树突状细胞。在本研究中,我们分析了树突状细胞是否支持免疫宿主中寄生虫的持续存在。免疫组织学研究和体外试验表明,在从硕大利什曼原虫感染中恢复的小鼠的淋巴结中,巨噬细胞和树突状细胞都含有活的寄生虫。然而,在没有外源性抗原的情况下,只有树突状细胞能够在体外诱导对硕大利什曼原虫的强烈T细胞免疫反应。体内进行的追踪实验表明,淋巴结中被感染的树突状细胞来源于从皮肤迁出的朗格汉斯细胞。数据表明,免疫动物淋巴结中被硕大利什曼原虫感染的树突状细胞和巨噬细胞代表长期宿主细胞,但只有树突状细胞有能力将内源性寄生虫抗原呈递给T细胞。长期被感染的树突状细胞因此可能允许持续刺激一群寄生虫特异性T细胞,保护小鼠免受再次感染。我们的结果支持这样的假说,即抗原的持续存在支持T细胞记忆的维持,并且树突状细胞在这一过程中起关键作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验