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自然杀伤细胞在调节树突状细胞对亚马逊利什曼原虫感染反应中的作用。

Role of natural killer cells in modulating dendritic cell responses to Leishmania amazonensis infection.

作者信息

Sanabria Mayra X Hernandez, Vargas-Inchaustegui Diego A, Xin Lijun, Soong Lynn

机构信息

Department of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX 77555-1070, USA.

出版信息

Infect Immun. 2008 Nov;76(11):5100-9. doi: 10.1128/IAI.00438-08. Epub 2008 Sep 15.

Abstract

The importance of the interaction between natural killer (NK) cells and dendritic cells (DCs) in the expansion of antiviral and antitumor immune responses is well-documented; however, limited information on DC-NK cell interaction during parasitic infections is available. Given that some Leishmania parasites are known to prevent or suppress DC activation, we developed a DC-NK cell coculture system to examine the role of NK cells in modulating the functions of Leishmania-infected DCs. We found that the addition of freshly isolated, resting NK cells significantly promoted the activation of DCs that were preinfected with Leishmania amazonensis promastigotes and that these activated DCs, in turn, stimulated NK cell activation mostly via cell contact-dependent mechanisms. Notably, L. amazonensis amastigote infection failed to activate DCs, and this lack of DC activation could be partially reversed by the addition of preactivated NK (ANK) cells but not resting NK cells. Moreover, the adoptive transfer of ANK cells into L. amazonensis-infected mice markedly increased DC and T-cell activation and reduced tissue parasite loads at 1 and 3 weeks postinfection. These results suggest differential roles of DC-NK cell cross talk at different stages of Leishmania infection and provide new insight into the interplay of components of the innate immune system during parasitic infection.

摘要

自然杀伤(NK)细胞与树突状细胞(DC)之间的相互作用在抗病毒和抗肿瘤免疫反应扩展中的重要性已有充分记载;然而,关于寄生虫感染期间DC-NK细胞相互作用的信息有限。鉴于已知一些利什曼原虫寄生虫可预防或抑制DC激活,我们开发了一种DC-NK细胞共培养系统,以研究NK细胞在调节感染利什曼原虫的DC功能中的作用。我们发现,添加新鲜分离的静息NK细胞可显著促进预先感染亚马逊利什曼原虫前鞭毛体的DC的激活,而这些激活的DC反过来主要通过细胞接触依赖性机制刺激NK细胞激活。值得注意的是,亚马逊利什曼原虫无鞭毛体感染未能激活DC,添加预激活的NK(ANK)细胞而非静息NK细胞可部分逆转这种DC激活的缺乏。此外,将ANK细胞过继转移到感染亚马逊利什曼原虫的小鼠体内,在感染后1周和3周时显著增加了DC和T细胞的激活,并降低了组织寄生虫负荷。这些结果表明,DC-NK细胞相互作用在利什曼原虫感染的不同阶段具有不同作用,并为寄生虫感染期间先天免疫系统各组分之间的相互作用提供了新的见解。

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