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使用体外猫免疫缺陷病毒模型的艾滋病疫苗研究:同源红细胞作为用于优先免疫假定保护性抗原的递送系统。

AIDS vaccination studies using an ex vivo feline immunodeficiency virus model: homologous erythrocytes as a delivery system for preferential immunization with putative protective antigens.

作者信息

Chiarantini L, Matteucci D, Pistello M, Mancini U, Mazzetti P, Massi C, Giannecchini S, Lonetti I, Magnani M, Bendinelli M

机构信息

Department of Biomedicine, University of Pisa, Italy.

出版信息

Clin Diagn Lab Immunol. 1998 Mar;5(2):235-41. doi: 10.1128/CDLI.5.2.235-241.1998.

Abstract

Feline immunodeficiency virus (FIV) is a useful model for testing of criteria for AIDS vaccine development. In the protocol we adopted, we used a primary isolate of FIV as a source of antigen and, for challenge, plasma from cats infected with the homologous virus never passaged in vitro. Cat erythrocytes (RBC) were coated with the surface components of freshly harvested and purified FIV by means of biotin-avidin-biotin bridges and used to immunize specific-pathogen-free cats (four doses at monthly intervals; total amount of FIV antigen administered per cat, approximately 14 microg). Immunized cats developed moderate levels of antibodies directed mainly to surface components of the virion and clearly evident lymphoproliferative responses. Four months after the last dose of immunogen, FIV-immunized cats and control cats immunized with bovine serum albumin-coated RBC were challenged. Judged from the results of the subsequent 12-month follow-up, FIV-immunized cats exhibited at least some degree of protection. However, following rechallenge, most of the FIV-immunized animals became virus positive in spite of a booster immunogen dose given 2 months before the second challenge.

摘要

猫免疫缺陷病毒(FIV)是用于测试艾滋病疫苗开发标准的有用模型。在我们采用的方案中,我们使用FIV的原始分离株作为抗原来源,并且在攻毒时,使用来自感染同源病毒且从未在体外传代的猫的血浆。通过生物素-抗生物素蛋白-生物素桥,将猫红细胞(RBC)用新鲜收获并纯化的FIV的表面成分包被,并用于免疫无特定病原体的猫(每月接种一剂,共四剂;每只猫接种的FIV抗原总量约为14微克)。免疫的猫产生了中等水平的抗体,主要针对病毒粒子的表面成分,并且有明显的淋巴细胞增殖反应。在最后一剂免疫原接种四个月后,对FIV免疫的猫和用牛血清白蛋白包被的RBC免疫的对照猫进行攻毒。从随后12个月的随访结果判断,FIV免疫的猫表现出至少一定程度的保护作用。然而,在再次攻毒后,尽管在第二次攻毒前2个月给予了加强免疫原剂量,但大多数FIV免疫的动物仍变为病毒阳性。

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