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弓形虫缓殖子形式的新型药物靶点 。 (注:原文“Novel Drug Targets for the Bradyzoite Form of.”后面似乎缺少具体所指生物,翻译可能不太完整准确,仅供参考。)

Novel Drug Targets for the Bradyzoite Form of .

作者信息

Ortiz Justin Orlando, Potter Anna K, Benmerzouga Imaan

机构信息

Kiran C. Patel College of Osteopathic Medicine, Department of Foundational Sciences, Clearwater, FL, USA.

出版信息

Res Rep Trop Med. 2025 Mar 29;16:25-30. doi: 10.2147/RRTM.S431290. eCollection 2025.

DOI:10.2147/RRTM.S431290
PMID:40176876
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11963886/
Abstract

is a world-wide parasite, with an estimated prevalence of approximately 30%. Toxoplasmosis is a severe disease in the immunocompromised, but few symptoms are exhibited by patients with an intact immune system, making this parasite a worldwide burden. Currently, few drugs exist in treating acute toxoplasmosis and no drugs exist to eliminate the bradyzoite of . Effective therapies against acute and chronic toxoplasmosis are urgently needed to reduce the burden of this disease. This review aims to give a summary of recent findings in the bradyzoite form of and the implication of these findings on drug development. A thorough search of PubMed and Google Scholar databases was used to identify studies within the past 10 years that illustrate targetable key elements in the differentiation and formation of the bradyzoite form of

摘要

是一种全球范围内的寄生虫,估计流行率约为30%。弓形虫病在免疫功能低下者中是一种严重疾病,但免疫系统完好的患者很少表现出症状,这使得这种寄生虫成为全球的一个负担。目前,治疗急性弓形虫病的药物很少,而且没有药物可以消除的缓殖子。迫切需要有效的急性和慢性弓形虫病治疗方法来减轻这种疾病的负担。本综述旨在总结关于缓殖子形式的最新研究结果以及这些发现对药物开发的意义。通过全面检索PubMed和谷歌学术数据库,以确定过去10年内阐述缓殖子形式的分化和形成中可作为靶点的关键要素的研究

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6461/11963886/9a9755b46f0a/RRTM-16-25-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6461/11963886/9a9755b46f0a/RRTM-16-25-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6461/11963886/9a9755b46f0a/RRTM-16-25-g0001.jpg

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本文引用的文献

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mBio. 2024 Sep 11;15(9):e0064124. doi: 10.1128/mbio.00641-24. Epub 2024 Aug 16.
2
chitinase-like protein TgCLP1 regulates the parasite cyst burden.几丁质酶样蛋白 TgCLP1 调节寄生虫包囊负荷。
Front Cell Infect Microbiol. 2024 May 17;14:1359888. doi: 10.3389/fcimb.2024.1359888. eCollection 2024.
3
Translation initiation factor eIF1.2 promotes Toxoplasma stage conversion by regulating levels of key differentiation factors.
翻译起始因子 eIF1.2 通过调节关键分化因子的水平促进弓形虫的阶段转换。
Nat Commun. 2024 May 23;15(1):4385. doi: 10.1038/s41467-024-48685-4.
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Identification of fungal natural products with potent inhibition in .鉴定具有强效抑制作用的真菌天然产物。
Microbiol Spectr. 2024 Apr 2;12(4):e0414223. doi: 10.1128/spectrum.04142-23. Epub 2024 Feb 29.
5
A transcriptional network required for bradyzoite development in Toxoplasma gondii is dispensable for recrudescent disease.一个在刚地弓形虫中进行缓殖子发育所必需的转录网络对于复发性疾病是可有可无的。
Nat Commun. 2023 Sep 28;14(1):6078. doi: 10.1038/s41467-023-40948-w.
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Nat Microbiol. 2023 May;8(5):889-904. doi: 10.1038/s41564-023-01358-2. Epub 2023 Apr 20.
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