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过去三十年(1987年至2017年)抗弓形虫药物及化合物对组织包囊的作用:一项系统评价

Activities of anti-Toxoplasma drugs and compounds against tissue cysts in the last three decades (1987 to 2017), a systematic review.

作者信息

Montazeri Mahbobeh, Mehrzadi Saeed, Sharif Mehdi, Sarvi Shahabeddin, Shahdin Shayesteh, Daryani Ahmad

机构信息

Toxoplasmosis Research Center, Mazandaran University of Medical Sciences, Sari, Iran.

Student Research Committee, Mazandaran University of Medical Sciences, Sari, Iran.

出版信息

Parasitol Res. 2018 Oct;117(10):3045-3057. doi: 10.1007/s00436-018-6027-z. Epub 2018 Aug 8.

Abstract

Currently, there is no approved therapy that can eradicate Toxoplasma gondii tissue cysts, which are responsible for chronic infection. This systematic review was performed to assess drugs or compounds that can be used as anti-T. gondii tissue cysts in vitro and in vivo. English electronic databases (i.e., PubMed, Science Direct, Scopus, Google Scholar, and Web of Science) were systematically searched for articles published up to 2017. A total of 55 papers published from 1987 to 2017 were eligible for inclusion in this systematic review. Among the drugs, atovaquone and azithromycin were found effective after long-term inoculation into mice; however, clinical cases of resistance to these drugs have been reported. Also, FR235222, QUI-11, tanshinone IIA, and hydroxyzine were shown to be effective against Toxoplasma cysts, but their effectiveness in vivo remains unknown. Additionally, compound 32, endochin-like quinolones, miltefosine, and guanabenz can be used as effective antiparasitic with the unique ability to reduce brain tissue cysts in chronically infected mice. Importantly, these antimicrobial agents are significant criteria for drug candidates. Future studies should focus on the biology and drug susceptibility of the cyst form of T. gondii in chronic toxoplasmosis patients to find more effective strategies that have sterilizing activity for eliminating T. gondii tissue cysts from the host, preventing disease relapse and potentially shortening the required duration of drug administration. Graphical abstract.

摘要

目前,尚无经批准的疗法能够根除导致慢性感染的弓形虫组织包囊。本系统评价旨在评估可在体外和体内用作抗弓形虫组织包囊的药物或化合物。对英文电子数据库(即PubMed、Science Direct、Scopus、谷歌学术和科学网)进行系统检索,查找截至2017年发表的文章。共有1987年至2017年发表的55篇论文符合纳入本系统评价的条件。在这些药物中,发现阿托伐醌和阿奇霉素在长期接种到小鼠体内后有效;然而,已有对这些药物耐药的临床病例报道。此外,FR235222、QUI-11、丹参酮IIA和羟嗪对弓形虫包囊显示出有效性,但其体内有效性尚不清楚。另外,化合物32、类内二氯喹啉、米替福新和胍那苄可作为有效的抗寄生虫药物,具有减少慢性感染小鼠脑组织包囊的独特能力。重要的是,这些抗菌剂是候选药物的重要标准。未来的研究应关注慢性弓形虫病患者中弓形虫包囊形式的生物学特性和药物敏感性,以找到更有效的策略,这些策略具有杀菌活性,可从宿主体内消除弓形虫组织包囊,预防疾病复发并可能缩短所需的给药持续时间。图形摘要。

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