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siRNA Therapeutics for the Therapy of COVID-19 and Other Coronaviruses.siRNA 治疗药物在 COVID-19 和其他冠状病毒治疗中的应用。
Mol Pharm. 2021 Jun 7;18(6):2105-2121. doi: 10.1021/acs.molpharmaceut.0c01239. Epub 2021 May 4.
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Ago2 protects siRNAs and microRNAs from target-directed degradation, even in the absence of 2'--methylation.AGO2 可保护 siRNAs 和 microRNAs 免受靶向降解,即使在没有 2'-O-甲基化的情况下也是如此。
RNA. 2021 Jun;27(6):710-724. doi: 10.1261/rna.078746.121. Epub 2021 Apr 14.
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Use-case scenarios for an anti-Cryptosporidium therapeutic.抗隐孢子虫治疗的应用场景。
PLoS Negl Trop Dis. 2021 Mar 11;15(3):e0009057. doi: 10.1371/journal.pntd.0009057. eCollection 2021 Mar.
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Therapeutic siRNA: state of the art.治疗性 siRNA:最新进展。
Signal Transduct Target Ther. 2020 Jun 19;5(1):101. doi: 10.1038/s41392-020-0207-x.
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Novel drug targets for treatment of cryptosporidiosis.新型抗隐孢子虫药物靶点。
Expert Opin Ther Targets. 2020 Sep;24(9):915-922. doi: 10.1080/14728222.2020.1785432. Epub 2020 Jul 7.
6
Cryptosporidium parvum cyclic GMP-dependent protein kinase (PKG): An essential mediator of merozoite egress.微小隐孢子虫环鸟苷酸依赖蛋白激酶(PKG):裂殖子外逸的必需介质。
Mol Biochem Parasitol. 2020 May;237:111277. doi: 10.1016/j.molbiopara.2020.111277. Epub 2020 Apr 26.
7
Clofazimine for Treatment of Cryptosporidiosis in Human Immunodeficiency Virus Infected Adults: An Experimental Medicine, Randomized, Double-blind, Placebo-controlled Phase 2a Trial.氯法齐明治疗人类免疫缺陷病毒感染成人隐孢子虫病:一项实验医学、随机、双盲、安慰剂对照 2a 期试验。
Clin Infect Dis. 2021 Jul 15;73(2):183-191. doi: 10.1093/cid/ciaa421.
8
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。
Proc Natl Acad Sci U S A. 2019 Oct 15;116(42):21160-21165. doi: 10.1073/pnas.1908239116. Epub 2019 Sep 30.
9
A Novel Method to Silence Genes in Cryptosporidium.一种沉默隐孢子虫基因的新方法。
Methods Mol Biol. 2020;2052:193-203. doi: 10.1007/978-1-4939-9748-0_11.
10
Systematic gene silencing identified Cryptosporidium nucleoside diphosphate kinase and other molecules as targets for suppression of parasite proliferation in human intestinal cells.系统基因沉默鉴定出隐孢子虫核苷二磷酸激酶和其他分子可作为抑制人肠道细胞寄生虫增殖的靶标。
Sci Rep. 2019 Aug 21;9(1):12153. doi: 10.1038/s41598-019-48544-z.

基于 RNA 的隐孢子虫感染治疗:概念验证研究。

RNA-Based Therapy for Cryptosporidium parvum Infection: Proof-of-Concept Studies.

机构信息

Department of Internal Medicine, Infectious Diseases Division, University of Texas Medical Branch, Galveston, Texas, USA.

出版信息

Infect Immun. 2022 Jul 21;90(7):e0019622. doi: 10.1128/iai.00196-22. Epub 2022 Jun 1.

DOI:10.1128/iai.00196-22
PMID:35647663
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9302151/
Abstract

is a leading cause of moderate-to-severe diarrhea in children, which is one of the major causes of death in children under 5 years old. Nitazoxanide is the only FDA-approved treatment for cryptosporidiosis. However, it has limited efficacy in immunosuppressed patients and malnourished children. Therefore, it is urgent to develop novel therapies against this parasite. RNA interference-mediated therapies are emerging as novel approaches for the treatment of infectious diseases. We have developed a novel method to silence essential genes in using single-stranded RNA (ssRNA)/Argonaute (Ago) complexes. In this work we conducted proof-of-concept studies to test the anticryptosporidial activity of these complexes by silencing Cryptosporidium parvum nucleoside diphosphate kinase (NDK) using and models. We demonstrated that a 3-day treatment with anti-sense NDK ssRNA/Ago decreased parasite burden by ~98% on infected cells. studies showed that ssRNA/Ago complexes encapsulated in lipid nanoparticles can be delivered onto intestinal epithelial cells of mice treated orally. In addition a cryptosporidiosis-mouse model showed that treatment with NDK ssRNA/Ago complexes reduced oocyst shedding in 4/5 SCID/beige mice during the acute phase of the infection. Our findings highlight the potential use of antisense RNA-based therapy as an alternative approach to cryptosporidiosis treatment.

摘要

是导致儿童中重度腹泻的主要原因之一,也是 5 岁以下儿童死亡的主要原因之一。硝唑尼特是唯一获得 FDA 批准用于治疗隐孢子虫病的药物。然而,它在免疫抑制患者和营养不良的儿童中的疗效有限。因此,迫切需要开发针对这种寄生虫的新型疗法。RNA 干扰介导的疗法作为治疗传染病的新方法正在出现。我们已经开发了一种新方法,使用单链 RNA(ssRNA)/Argonaute(Ago)复合物沉默 中的必需基因。在这项工作中,我们通过使用 和 模型沉默隐孢子虫微小二磷酸核苷激酶(NDK)来进行概念验证研究,以测试这些复合物的抗隐孢子虫活性。我们证明,用抗 NDK ssRNA/Ago 处理 3 天可使感染细胞中的寄生虫载量减少约 98%。细胞摄取研究表明,包封在脂质纳米颗粒中的 ssRNA/Ago 复合物可以通过口服给药递送到经处理的小鼠肠上皮细胞上。此外,隐孢子虫病小鼠模型显示,在感染的急性期,用 NDK ssRNA/Ago 复合物治疗可使 4/5 只 SCID/beige 小鼠的卵囊脱落减少。我们的研究结果强调了基于反义 RNA 的治疗作为隐孢子虫病治疗替代方法的潜在用途。