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针对皮肤利什曼病的疫苗研发。皮下接种减毒寄生虫可保护CBA小鼠免受强毒力硕大利什曼原虫的攻击。

Vaccine development against cutaneous leishmaniasis. Subcutaneous administration of radioattenuated parasites protects CBA mice against virulent Leishmania major challenge.

作者信息

Rivier D, Shah R, Bovay P, Mauel J

机构信息

Institute of Biochemistry, University of Lausanne, Epalinges, Switzerland.

出版信息

Parasite Immunol. 1993 Feb;15(2):75-84. doi: 10.1111/j.1365-3024.1993.tb00587.x.

DOI:10.1111/j.1365-3024.1993.tb00587.x
PMID:8446467
Abstract

Experiments described in this paper were aimed at determining whether subcutaneous inoculation of live, avirulent Leishmania major would protect mice against infection by the virulent parasite. To this effect, promastigotes or amastigotes of a highly virulent strain of L. major (MRHO/IR/76), used in human trials of leishmanization, and which induces non-healing skin lesions in both CBA and BALB/c mice, were rendered non-pathogenic by gamma irradiation. A dose of 150 krad was required to abrogate the virulence of the parasite as tested on BALB/c mice. Strikingly, however, not all leishmanias were completely inactivated by this procedure since live parasites were detected in the footpads and/or the inguinal lymph nodes as long as 28 days (CBA) or 18 weeks (BALB/c) after injection. Furthermore, 150 krad-irradiated promastigotes retained the capacity to transform into amastigotes intracellularly in vitro. Subcutaneous inoculation of this irradiated 'vaccine' conferred onto CBA mice a high degree of protection against challenge by both the homologous and a heterologous (MRHO/SU/59/P) strains of L. major. Lymph node cells from protected animals acquired the capacity to activate infected macrophages in vitro to kill intracellular L. major. To allow for maximum development of immunoprotection, the irradiated promastigotes had to remain viable, perhaps reflecting a requirement for transformation into amastigotes in the vaccinated host.

摘要

本文所述实验旨在确定皮下接种活的、无毒力的硕大利什曼原虫是否能保护小鼠免受强毒寄生虫的感染。为此,在人类皮肤利什曼病接种试验中使用的、能在CBA和BALB/c小鼠中诱导不愈合皮肤病变的硕大利什曼原虫(MRHO/IR/76)强毒株的前鞭毛体或无鞭毛体,经γ射线辐照后变为无致病性。经测试,对BALB/c小鼠而言,需要150千拉德的剂量才能消除该寄生虫的毒力。然而,令人惊讶的是,并非所有利什曼原虫都因该程序而完全失活,因为在注射后长达28天(CBA小鼠)或18周(BALB/c小鼠)的脚垫和/或腹股沟淋巴结中仍能检测到活的寄生虫。此外,经150千拉德辐照的前鞭毛体在体外仍保留在细胞内转化为无鞭毛体的能力。皮下接种这种辐照“疫苗”能使CBA小鼠对同源和异源(MRHO/SU/59/P)硕大利什曼原虫株的攻击产生高度保护作用。来自受保护动物的淋巴结细胞在体外获得了激活受感染巨噬细胞以杀死细胞内硕大利什曼原虫的能力。为了使免疫保护作用得到最大程度的发挥,辐照后的前鞭毛体必须保持存活,这可能反映出在接种宿主中转化为无鞭毛体的必要性。

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