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用明矾沉淀的重组钩虫分泌蛋白1进行疫苗接种可保护小鼠免受感染性钩虫(犬钩虫)幼虫的攻击感染。

Vaccination with alum-precipitated recombinant Ancylostoma-secreted protein 1 protects mice against challenge infections with infective hookworm (Ancylostoma caninum) larvae.

作者信息

Ghosh K, Hawdon J, Hotez P

机构信息

Department of Pediatrics (Infectious Diseases Division), Yale University School of Medicine, New Haven, Connecticut 06520, USA.

出版信息

J Infect Dis. 1996 Dec;174(6):1380-3. doi: 10.1093/infdis/174.6.1380.

Abstract

Ancylostoma-secreted protein 1 (ASP-1) is the major protein secreted by infective hookworm larvae (Ancylostoma caninum). The Escherichia coli-expressed recombinant protein was evaluated as a vaccine antigen in a mouse model of ancylostomiasis. A. caninum larvae migrate through mouse lungs, with maximal migration occurring 48-54 h after oral infection. Quantitative larval recovery from the lungs at this time was used as an end point for vaccine evaluation. All mice developed antibodies to recombinant ASP-1 (rASP-1) after immunization and boosting with the alum-precipitated protein. The immunized mice had their worm burden reduced 79% (P < .0001) compared with controls. Immunization with rASP-1 in the presence of Corynebacterium parvum adjuvant also showed a vaccine effect (63% protection; P < .0001). The possibility that this protective effect resulted from delayed larval lung entry was excluded. rASP-1 offers promise as a hookworm vaccine antigen.

摘要

钩虫分泌蛋白1(ASP-1)是感染性钩虫幼虫(犬钩口线虫)分泌的主要蛋白质。在犬钩口线虫病小鼠模型中,对大肠杆菌表达的重组蛋白作为疫苗抗原进行了评估。犬钩口线虫幼虫在小鼠肺部移行,口服感染后48-54小时移行达到高峰。此时从肺部定量回收幼虫作为疫苗评估的终点。所有小鼠在用明矾沉淀蛋白免疫和加强免疫后均产生了针对重组ASP-1(rASP-1)的抗体。与对照组相比,免疫小鼠的虫负荷降低了79%(P <.0001)。在短小棒状杆菌佐剂存在的情况下用rASP-1免疫也显示出疫苗效果(63%的保护率;P <.0001)。排除了这种保护作用是由于幼虫进入肺部延迟所致的可能性。rASP-1有望成为一种钩虫疫苗抗原。

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