Layland Laura E, Ajendra Jesuthas, Ritter Manuel, Wiszniewsky Anna, Hoerauf Achim, Hübner Marc P
Institute of Medical Microbiology, Immunology and Parasitology (IMMIP), University Hospital of Bonn, Sigmund Freud Straße 25, Bonn, 53105, Germany.
Parasit Vectors. 2015 Jul 25;8:396. doi: 10.1186/s13071-015-1011-2.
One of the most advantageous research aspects of the murine model of filariasis, Litomosoides sigmodontis, is the availability of mouse strains with varying susceptibility to the nematode infection. In C57BL/6 mice, L. sigmodontis worms are largely eliminated in this strain by day 40 post-infection and never produce their offspring, microfilariae (Mf). This provides a unique opportunity to decipher potential immune pathways that are required by filariae to achieve a successful infection. In this study we tracked worm development and patency, the production of microfilariae and thus the transmission life-stage, in Rag2IL-2Rγ(-/-) mice which are deficient in T, B and NK cell populations.
Although worm burden was comparable between wildtype (WT) and Rag2IL-2Rγ(-/-) mice on d30, by day 72 post-infection, parasites in Rag2IL-2Rγ(-/-) mice were still in abundance, freely motile and all mice presented high quantities of Mf both at the site of infection, the thoracic cavity (TC), and in peripheral blood. Levels of cytokine (IL-4, IL-6, TNFα) and chemokine (MIP-2, RANTES, Eotaxin) parameters were generally low in the TC of infected Rag2IL-2Rγ(-/-)mice at both time-points. The frequency of neutrophils however was higher in Rag2IL-2Rγ(-/-)mice whereas eosinophils and macrophage populations, including alternatively activated macrophages, were elevated in WT controls.
Our data highlight that adaptive immune responses prevent the development of patent L. sigmodontis infections in semi-susceptible C57BL/6 mice and suggest that induction of such responses may offer a strategy to prevent transmission of human filariasis.
丝虫病小鼠模型——巴西日圆线虫(Litomosoides sigmodontis)最具优势的研究方面之一,是存在对该线虫感染敏感性不同的小鼠品系。在C57BL/6小鼠中,感染后第40天,巴西日圆线虫在很大程度上被该品系清除,且从未产生其后代——微丝蚴(Mf)。这提供了一个独特的机会来解读丝虫成功感染所需的潜在免疫途径。在本研究中,我们追踪了T、B和NK细胞群均有缺陷的Rag2IL-2Rγ(-/-)小鼠体内蠕虫的发育及成虫期、微丝蚴的产生以及因此而来的传播生命周期阶段。
虽然在感染后第30天野生型(WT)小鼠和Rag2IL-2Rγ(-/-)小鼠的蠕虫负荷相当,但到感染后第72天,Rag2IL-2Rγ(-/-)小鼠体内的寄生虫仍然大量存在、活动自如,并且所有小鼠在感染部位胸腔(TC)和外周血中均呈现出大量微丝蚴。在两个时间点,感染的Rag2IL-2Rγ(-/-)小鼠胸腔内细胞因子(IL-4、IL-6、TNFα)和趋化因子(MIP-2、RANTES、嗜酸性粒细胞趋化因子)参数水平通常较低。然而,Rag2IL-2Rγ(-/-)小鼠体内中性粒细胞的频率较高,而野生型对照组中嗜酸性粒细胞和巨噬细胞群体(包括交替活化的巨噬细胞)有所增加。
我们的数据表明,适应性免疫反应可阻止半易感C57BL/6小鼠发生巴西日圆线虫显性感染,并提示诱导此类反应可能提供一种预防人类丝虫病传播的策略。