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加密货币:投资新模式以推进感染与免疫研究。

Crypto-Currency: Investing in New Models to Advance the Study of Infection and Immunity.

机构信息

Cryptosporidiosis Laboratory, The Francis Crick Institute, London, United Kingdom.

出版信息

Front Cell Infect Microbiol. 2020 Nov 18;10:587296. doi: 10.3389/fcimb.2020.587296. eCollection 2020.

DOI:10.3389/fcimb.2020.587296
PMID:33312965
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7708325/
Abstract

Cryptosporidiosis is a leading cause of diarrheal disease and an important contributor to global morbidity and mortality. Although the brunt of disease burden is felt by children in developing countries, is a ubiquitous intestinal parasite with frequent outbreaks around the world. There are no consistently effective treatments for cryptosporidiosis and the research to drive new developments has stagnated, largely due to a lack of efficient and models. Fortunately, these research barriers have started to fall. In this review, we highlight two recent advances aiding this process: A tractable mouse model for infection and stem cell-based culture systems that mimic the complexity of the host intestine. These models are paving the way for researchers to investigate infection and host immunity down to a molecular level. We believe that wise investments made to adopt and develop these new models will reap benefits not only for the community but also for the intestinal immunology field at large.

摘要

隐孢子虫病是腹泻病的主要病因,也是全球发病率和死亡率的重要因素。尽管发展中国家的儿童是疾病负担的主要人群,但 是一种无处不在的肠道寄生虫,在世界各地经常爆发。目前还没有针对隐孢子虫病的有效治疗方法,推动新发展的研究已经停滞不前,主要是因为缺乏有效的 和 模型。幸运的是,这些研究障碍开始被打破。在这篇综述中,我们强调了两个最近的进展,它们有助于推动这一进程:一种用于 感染的可处理的小鼠模型和模拟宿主肠道复杂性的基于干细胞的 培养系统。这些模型为研究人员提供了一条途径,可在分子水平上研究 感染和宿主免疫。我们相信,明智地投资于采用和开发这些新模型不仅将使 界受益,也将使整个肠道免疫学领域受益。

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本文引用的文献

1
A Conditional Protein Degradation System To Study Essential Gene Function in Cryptosporidium parvum.一种条件性蛋白降解系统,用于研究微小隐孢子虫中必需基因的功能。
mBio. 2020 Aug 25;11(4):e01231-20. doi: 10.1128/mBio.01231-20.
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Organoids in immunological research.类器官在免疫学研究中的应用。
Nat Rev Immunol. 2020 May;20(5):279-293. doi: 10.1038/s41577-019-0248-y. Epub 2019 Dec 18.
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Genetic ablation of purine salvage in reveals nucleotide uptake from the host cell.嘌呤补救途径的遗传消融揭示了从宿主细胞摄取核苷酸。
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下一代测序技术在研究中的利与弊。
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Life cycle progression and sexual development of the apicomplexan parasite Cryptosporidium parvum.顶复门寄生虫微小隐孢子虫的生活史进展和性发育。
Nat Microbiol. 2019 Dec;4(12):2226-2236. doi: 10.1038/s41564-019-0539-x. Epub 2019 Sep 2.
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A Stem-Cell-Derived Platform Enables Complete Cryptosporidium Development In Vitro and Genetic Tractability.基于干细胞的平台可实现体外完整隐孢子虫发育和遗传操作性。
Cell Host Microbe. 2019 Jul 10;26(1):123-134.e8. doi: 10.1016/j.chom.2019.05.007. Epub 2019 Jun 20.
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A Genetically Tractable, Natural Mouse Model of Cryptosporidiosis Offers Insights into Host Protective Immunity.一种遗传可操作的、天然的隐孢子虫病小鼠模型为宿主保护性免疫提供了新见解。
Cell Host Microbe. 2019 Jul 10;26(1):135-146.e5. doi: 10.1016/j.chom.2019.05.006. Epub 2019 Jun 20.
7
A suite of phenotypic assays to ensure pipeline diversity when prioritizing drug-like Cryptosporidium growth inhibitors.当优先考虑具有类药性的隐孢子虫生长抑制剂时,采用一组表型测定法来确保候选药物多样性。
Nat Commun. 2019 Apr 23;10(1):1862. doi: 10.1038/s41467-019-09880-w.
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Progress and potential in organoid research.类器官研究的进展与潜力。
Nat Rev Genet. 2018 Nov;19(11):671-687. doi: 10.1038/s41576-018-0051-9.
9
Widespread occurrence of Cryptosporidium infections in patients with HIV/AIDS: Epidemiology, clinical feature, diagnosis, and therapy.隐孢子虫感染在艾滋病患者中的广泛发生:流行病学、临床特征、诊断与治疗
Acta Trop. 2018 Nov;187:257-263. doi: 10.1016/j.actatropica.2018.08.018. Epub 2018 Aug 15.
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Modelling Cryptosporidium infection in human small intestinal and lung organoids.建模人类小肠和肺类器官中的隐孢子虫感染。
Nat Microbiol. 2018 Jul;3(7):814-823. doi: 10.1038/s41564-018-0177-8. Epub 2018 Jun 25.