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作为针对球虫寄生虫艾美耳球虫、弓形虫和新孢子虫的控制策略的疫苗接种

Vaccination as a control strategy against the coccidial parasites Eimeria, Toxoplasma and Neospora.

作者信息

Innes E A, Vermeulen A N

机构信息

Moredun Research Institute, Pentlands Science Park, Edinburgh EH26 OPZ, UK.

出版信息

Parasitology. 2006;133 Suppl:S145-68. doi: 10.1017/S0031182006001855.

Abstract

The protozoan parasites Eimeria spp. Toxoplasma gondii and Neospora caninum are significant causes of disease in livestock worldwide and T. gondii is also an important human pathogen. Drugs have been used with varying success to help control aspects of these diseases and commercial vaccines are available for all three groups of parasites. However, there are issues with increasing development of resistance to many of the anti-coccidial drugs used to help control avian eimeriosis and public concerns about the use of drugs in food animals. In addition there are no drugs available that can act against the tissue cyst stage of either T. gondii or N. caninum and thus cure animals or people of infection. All three groups of parasites multiply within the cells of their host species and therefore cell mediated immune mechanisms are thought to be an important component of host protective immunity. Successful vaccination strategies for both Eimeria and Toxoplasma have relied on using a live vaccination approach using attenuated parasites which allows correct processing and presentation of antigen to the host immune system to stimulate appropriate cell mediated immune responses. However, live vaccines can have problems with safety, short shelf-life and large-scale production; therefore there is continued interest in devising new vaccines using defined recombinant antigens. The major challenges in devising novel vaccines are to select relevant antigens and then present them to the immune system in an appropriate manner to enable the induction of protective immune responses. With all three groups of parasites, vaccine preparations comprising antigens from the different life cycle stages may also be advantageous. In the case of Eimeria parasites there are also problems with strain-specific immunity therefore a cocktail of antigens from different parasite strains may be required. Improving our knowledge of the different parasite transmission routes, host-parasite relationships, disease pathogenesis and determining the various roles of the host immune response being at times host-protective, parasite protective and in causing immunopathology will help to tailor a vaccination strategy against a particular disease target. This paper discusses current vaccination strategies to help combat infections with Eimeria, Toxoplasma and Neospora and recent research looking towards developing new vaccine targets and approaches.

摘要

原生动物寄生虫艾美耳属、刚地弓形虫和犬新孢子虫是全球家畜疾病的重要病因,刚地弓形虫也是一种重要的人类病原体。药物在控制这些疾病方面取得了不同程度的成功,并且有针对这三类寄生虫的商业疫苗。然而,用于控制禽艾美耳球虫病的许多抗球虫药物的耐药性不断增加,以及公众对食用动物使用药物的担忧,这些都存在问题。此外,目前没有药物能够作用于刚地弓形虫或犬新孢子虫的组织包囊阶段,因此无法治愈感染的动物或人类。这三类寄生虫均在其宿主细胞内繁殖,因此细胞介导的免疫机制被认为是宿主保护性免疫的重要组成部分。针对艾美耳球虫和弓形虫的成功疫苗接种策略依赖于使用减毒寄生虫的活疫苗接种方法,这种方法能够将抗原正确加工并呈递给宿主免疫系统,以刺激适当的细胞介导免疫反应。然而,活疫苗存在安全性、保质期短和大规模生产等问题;因此,人们持续关注使用特定重组抗原来设计新疫苗。设计新型疫苗的主要挑战在于选择相关抗原,然后以适当方式将其呈递给免疫系统,以诱导保护性免疫反应。对于这三类寄生虫而言,包含来自不同生命周期阶段抗原的疫苗制剂可能也具有优势。就艾美耳属寄生虫而言,还存在菌株特异性免疫的问题,因此可能需要来自不同寄生虫菌株的抗原混合物。增进我们对不同寄生虫传播途径、宿主 - 寄生虫关系、疾病发病机制的了解,并确定宿主免疫反应有时具有宿主保护、寄生虫保护以及导致免疫病理等各种作用,这将有助于制定针对特定疾病目标的疫苗接种策略。本文讨论了当前用于对抗艾美耳球虫、弓形虫和新孢子虫感染的疫苗接种策略,以及近期针对开发新疫苗靶点和方法的研究。

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