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亚马逊利什曼原虫-BALB/c小鼠模型中唾液介导的保护性免疫的白蛉特异性

Sand fly specificity of saliva-mediated protective immunity in Leishmania amazonensis-BALB/c mouse model.

作者信息

Thiakaki Maria, Rohousova Iva, Volfova Vera, Volf Petr, Chang Kwang-Poo, Soteriadou Ketty

机构信息

Department of Microbiology, Laboratory of Molecular Parasitology, Hellenic Pasteur Institute, 127 Bas. Sofias Ave., 11521 Athens, Greece.

出版信息

Microbes Infect. 2005 Apr;7(4):760-6. doi: 10.1016/j.micinf.2005.01.013. Epub 2005 Apr 9.

Abstract

Immune response of BALB/c mice to the salivary antigens of sand flies was found to vary with different species used, i.e. Phlebotomus papatasi, Phlebotomus sergenti and Lutzomyia longipalpis. Exposure of mice to bites of these sand flies elicits production of antibodies, which are largely specific to different saliva antigens previously identified as unique to the respective fly species. When immunized intradermally (i.d.) with salivary gland lysates (SGL) of L. longipalpis, BALB/c mice developed partial protective immunity against challenges in the contralateral ears with Leishmania amazonensis plus the gland lysates. Preimmunization of these mice with the lysates from the other two species was ineffective, further indicative of the specificity of saliva-mediated immune response. The partial protective immunity observed is significant, although it is not as dramatic as reported previously in a different sand fly-mouse model. There is a correlation of this immunity with a lower number of mononuclear and polymorphonuclear phagocytes at the site of parasite inoculation. Vector species-specificity of this immunity implies its elicitation by unique saliva antigen-an issue which requires attention when designing saliva-based vaccines against leishmaniasis.

摘要

研究发现,BALB/c小鼠对不同种类白蛉唾液抗原的免疫反应有所不同,这些白蛉种类包括巴氏白蛉、赛氏白蛉和长须罗蛉。让小鼠暴露于这些白蛉的叮咬之下会引发抗体产生,这些抗体在很大程度上针对先前已确定为各白蛉物种所特有的不同唾液抗原。当用长须罗蛉的唾液腺裂解物进行皮内免疫时,BALB/c小鼠对用亚马逊利什曼原虫加该腺体裂解物对其对侧耳朵进行的攻击产生了部分保护性免疫。用另外两个物种的裂解物对这些小鼠进行预先免疫无效,这进一步表明了唾液介导的免疫反应的特异性。观察到的部分保护性免疫是显著的,尽管它不像先前在另一种白蛉-小鼠模型中报道的那样显著。这种免疫与寄生虫接种部位单核和多形核吞噬细胞数量减少相关。这种免疫的媒介物种特异性意味着它是由独特的唾液抗原引发的——这是在设计针对利什曼病的基于唾液的疫苗时需要关注的一个问题。

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