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弓形虫抗原的系统评价,以寻找最佳的疫苗候选物进行免疫。

A systematic review of Toxoplasma gondii antigens to find the best vaccine candidates for immunization.

机构信息

Toxoplasmosis Research Center, Mazandaran University of Medical Sciences, Sari, Iran; Department of Parasitology & Mycology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran; Students Research Committee, Department of Parasitology and Mycology, School of Medicine, Mazandaran University of Medical Sciences, Sari, Iran.

Toxoplasmosis Research Center, Mazandaran University of Medical Sciences, Sari, Iran; Department of Parasitology, Sari Medical School, Mazandaran University of Medical Sciences, Sari, Iran.

出版信息

Microb Pathog. 2019 Jan;126:172-184. doi: 10.1016/j.micpath.2018.11.003. Epub 2018 Nov 3.

Abstract

At present, there is not any available accepted vaccine for prevention of Toxoplasma gondii (T. gondii) in human and animals. We conducted literature search through English (Google Scholar, PubMed, Science Direct, Scopus, EBSCO, ISI Web of Science) scientific paper databases to find the best vaccine candidates against toxoplasmosis among T. gondii antigens. Articles with information on infective stage, pathogenicity, immunogenicity and characterization of antigens were selected. We considered that the ideal and significant vaccines should include different antigens and been expressed in all infective stages of the parasite with a high pathogenicity and immunogenicity. Evaluation within this systematic review indicates that MIC 3, 4, 13, ROP 2, RON 5, GRA 1, 6, 8, 14 are expressed in all three infective stages and have pathogenicity and immunogenicity. MIC 5, ROM 4, GRA 2, 4, 15, ROP 5, 16, 17, 38, RON 4, MIC 1, GRA 10, 12, 16, SAG 3 are expressed in only tachyzoites and bradyzoites stages of T. gondii with pathogenicity/immunogenicity. Some antigens appeared to be expressed in a single stage (tachyzoites) but have high pathogenicity and induce immune response. They include enolase2 (ENO2), SAG 1, SAG5D, HSP 70, ROM 1, ROM 5, AMA 1, ROP 18, RON2 and GRA 24. In conclusion, current vaccination against T. gondii infection is not satisfactory, and with the increasing number of high-risk individuals, the development of an effective and safe specific vaccine is greatly valuable for toxoplasmosis prevention. This systematic review reveals prepare candidates for immunization studies.

摘要

目前,尚无用于预防弓形虫(Toxoplasma gondii,T. gondii)的人用和动物用疫苗。我们通过英文(Google Scholar、PubMed、Science Direct、Scopus、EBSCO、ISI Web of Science)科学论文数据库进行文献检索,以找到针对弓形虫病的最佳疫苗候选物。选择了具有感染阶段、致病性、免疫原性和抗原特征信息的文章。我们认为,理想和重要的疫苗应包括不同的抗原,并在寄生虫的所有感染阶段表达,具有高致病性和免疫原性。这项系统评价中的评估表明,MIC 3、4、13、ROP 2、RON 5、GRA 1、6、8、14 在所有三个感染阶段均有表达,具有致病性和免疫原性。MIC 5、ROM 4、GRA 2、4、15、ROP 5、16、17、38、RON 4、MIC 1、GRA 10、12、16、SAG 3 仅在弓形虫的速殖子和缓殖子阶段表达,具有致病性/免疫原性。一些抗原似乎仅在一个阶段(速殖子)表达,但具有高致病性并诱导免疫反应。它们包括烯醇酶 2(ENO2)、SAG 1、SAG5D、HSP 70、ROM 1、ROM 5、AMA 1、ROP 18、RON2 和 GRA 24。总之,目前针对 T. gondii 感染的疫苗接种效果并不令人满意,随着高危人群的增加,开发一种有效和安全的特异性疫苗对于预防弓形虫病具有重要价值。这项系统评价揭示了针对弓形虫病免疫研究的候选疫苗。

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