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经口感染克氏锥虫会引发系统性 CD8+T 细胞应答,并对异位挑战产生保护作用。

Oral exposure to Trypanosoma cruzi elicits a systemic CD8⁺ T cell response and protection against heterotopic challenge.

机构信息

Department of Cellular Biology and Center for Tropical and Emerging Global Diseases, University of Georgia, Athens, GA 30502, USA.

出版信息

Infect Immun. 2011 Aug;79(8):3397-406. doi: 10.1128/IAI.01080-10. Epub 2011 May 31.

Abstract

Trypanosoma cruzi infects millions of people in Latin America and often leads to the development of Chagas disease. T. cruzi infection can be acquired at or near the bite site of the triatomine vector, but per os infection is also a well-documented mode of transmission, as evidenced by recent microepidemics of acute Chagas disease attributed to the consumption of parasite-contaminated foods and liquids. It would also be convenient to deliver vaccines for T. cruzi by the oral route, particularly live parasite vaccines intended for the immunization of reservoir hosts. For these reasons, we were interested in better understanding immunity to T. cruzi following oral infection or oral vaccination, knowing that the route of infection and site of antigen encounter can have substantial effects on the ensuing immune response. Here, we show that the route of infection does not alter the ability of T. cruzi to establish infection in muscle tissue nor does it impair the generation of a robust CD8(+) T cell response. Importantly, oral vaccination with attenuated parasites provides protection against wild-type (WT) T. cruzi challenge. These results strongly support the development of whole-organism-based vaccines targeting reservoir species as a means to alleviate the burden of Chagas disease in affected regions.

摘要

克氏锥虫感染拉丁美洲数百万人,常导致恰加斯病的发生。克氏锥虫感染可在感染传播媒介三锥虫的叮咬部位或附近获得,但经口感染也是一种有据可查的传播方式,最近因食用受寄生虫污染的食物和液体而导致的急性恰加斯病微流行就证明了这一点。通过口服途径来输送针对克氏锥虫的疫苗也很方便,特别是针对储存宿主的免疫接种的活寄生虫疫苗。出于这些原因,我们有兴趣更好地了解经口感染或口服疫苗接种后对克氏锥虫的免疫反应,因为我们知道感染途径和抗原接触部位会对随后的免疫反应产生重大影响。在这里,我们表明感染途径不会改变克氏锥虫在肌肉组织中建立感染的能力,也不会损害产生强大 CD8+T 细胞反应的能力。重要的是,用减毒寄生虫进行口服疫苗接种可提供针对野生型(WT)克氏锥虫挑战的保护。这些结果有力地支持了针对储存物种的基于全生物体疫苗的开发,作为减轻受影响地区恰加斯病负担的一种手段。

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