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鸟分枝杆菌复合群能够损伤树突状细胞的成熟。

Mycobacterium avium subspecies impair dendritic cell maturation.

机构信息

1Institute for Microbiology, Department of Infectious Diseases, University of Veterinary Medicine Hannover, Hannover, Germany.

出版信息

Innate Immun. 2013 Oct;19(5):451-61. doi: 10.1177/1753425912470291. Epub 2013 Jan 2.

DOI:10.1177/1753425912470291
PMID:23283733
Abstract

Mycobacterium avium ssp. paratuberculosis (MAP) causes Johne's disease, a chronic, granulomatous enteritis of ruminants. Dendritic cells (DC) of the gut are ideally placed to combat invading mycobacteria; however, little is known about their interaction with MAP. Here, we investigated the interaction of MAP and the closely related M. avium ssp. avium (MAA) with murine DC and the effect of infected macrophages on DC maturation. The infection of DC with MAP or MAA induced DC maturation, which differed to that of LPS as maturation was accompanied by higher production of IL-10 and lower production of IL-12. Treatment of maturing DC with supernatants from mycobacteria-infected macrophages resulted in impaired DC maturation, leading to a semi-mature, tolerogenic DC phenotype expressing low levels of MHCII, CD86 and TNF-α after LPS stimulation. Though the cells were not completely differentiated they responded with an increased IL-10 and a decreased IL-12 production. Using recombinant cytokines we provide evidence that the semi-mature DC phenotype results from a combination of secreted cytokines and released antigenic mycobacterial components of the infected macrophage. Our results indicate that MAP and MAA are able to subvert DC function directly by infecting and indirectly via the milieu created by infected macrophages.

摘要

分支杆菌 avium ssp. paratuberculosis(MAP)引起 Johne 病,一种反刍动物的慢性肉芽肿性肠炎。肠道树突状细胞(DC)是对抗入侵分枝杆菌的理想位置;然而,人们对它们与 MAP 的相互作用知之甚少。在这里,我们研究了 MAP 和密切相关的 M. avium ssp. avium(MAA)与小鼠 DC 的相互作用以及受感染的巨噬细胞对 DC 成熟的影响。MAP 或 MAA 感染 DC 诱导 DC 成熟,这与 LPS 不同,因为成熟伴随着更高水平的 IL-10 和更低水平的 IL-12 产生。用来自分枝杆菌感染的巨噬细胞的上清液处理成熟的 DC 导致 DC 成熟受损,导致半成熟、耐受性 DC 表型,在 LPS 刺激后表达低水平的 MHCII、CD86 和 TNF-α。尽管这些细胞没有完全分化,但它们的反应是增加 IL-10 和减少 IL-12 的产生。使用重组细胞因子,我们提供了证据表明,半成熟的 DC 表型是由受感染的巨噬细胞分泌的细胞因子和释放的抗原性分枝杆菌成分的组合引起的。我们的结果表明,MAP 和 MAA 能够通过感染直接和通过受感染的巨噬细胞产生的环境间接颠覆 DC 功能。

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