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婴儿利什曼原虫酸性核糖体蛋白LiP2a在体内诱导显著的体液反应,并在体外刺激细胞增殖以及小鼠脾细胞产生γ干扰素(IFN-γ)。

The Leishmania infantum acidic ribosomal protein LiP2a induces a prominent humoral response in vivo and stimulates cell proliferation in vitro and interferon-gamma (IFN-gamma) production by murine splenocytes.

作者信息

Soto M, Alonso C, Requena J M

机构信息

Centro de Biología Molecular Severo Ochoa, Universidad Autónoma de Madrid, Spain.

出版信息

Clin Exp Immunol. 2000 Nov;122(2):212-8. doi: 10.1046/j.1365-2249.2000.01372.x.

Abstract

The acidic ribosomal proteins of the protozoan parasite Leishmania infantum have been described as prominent antigens during both human and canine visceral leishmaniasis. In this study we present data showing that the intraperitoneal administration in BALB/c mice of the Leishmania LiP2a protein, in the absence of any added adjuvants, elicited a strong humoral response as an indication that the protein is a potent immunogen. Despite the evolutionary conservation of the acidic ribosomal proteins, the antibody response was found to be specific for the Leishmania protein. Another remarkable finding was the observation that the LiP2a protein stimulates the in vitro proliferation of splenocytes from either LiP2a-immunized or naive BALB/c mice. Since similar proliferative indices were observed in T cell-enriched cultures, it is likely that the LiP2a stimulating activity is due mainly to T lymphocyte expansion. Also, the stimulatory effect was demonstrated to be antigen-specific, since the proliferation was abrogated by the presence of anti-LiP2a antibodies. Interestingly, the LiP2a protein stimulated the production of substantial amounts of IFN-gamma in cultured splenocytes from LiP2a-immunized mice. Our data indicate therefore that the immunostimulatory properties shown by this antigen should be taken into account when developing therapeutic and prophylactic vaccines against leishmaniasis.

摘要

原生动物寄生虫婴儿利什曼原虫的酸性核糖体蛋白已被描述为人类和犬内脏利什曼病期间的主要抗原。在本研究中,我们提供的数据表明,在不添加任何佐剂的情况下,向BALB/c小鼠腹腔注射利什曼原虫LiP2a蛋白可引发强烈的体液反应,这表明该蛋白是一种有效的免疫原。尽管酸性核糖体蛋白在进化上具有保守性,但发现抗体反应对利什曼原虫蛋白具有特异性。另一个显著发现是观察到LiP2a蛋白刺激来自LiP2a免疫或未免疫的BALB/c小鼠的脾细胞在体外增殖。由于在富含T细胞的培养物中观察到类似的增殖指数,LiP2a的刺激活性可能主要归因于T淋巴细胞的扩增。此外,由于抗LiP2a抗体的存在消除了增殖,因此证明刺激作用具有抗原特异性。有趣的是,LiP2a蛋白刺激来自LiP2a免疫小鼠的培养脾细胞产生大量的IFN-γ。因此,我们的数据表明,在开发针对利什曼病的治疗性和预防性疫苗时,应考虑该抗原所显示的免疫刺激特性。

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