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RNA 干扰作为慢性乙型肝炎病毒感染治疗方法的研究进展。

Progress in the use of RNA interference as a therapy for chronic hepatitis B virus infection.

机构信息

Antiviral Gene Therapy Research Unit, Department of Molecular Medicine and Haematology, University of the Witwatersrand Medical School, WITS 2050, South Africa.

出版信息

Genome Med. 2010 Apr 28;2(4):28. doi: 10.1186/gm149.

Abstract

Chronic infection with hepatitis B virus (HBV) occurs in approximately 6% of the world's population and carriers of the virus are at risk for hepatocellular carcinoma and cirrhosis. Current treatment regimens, which include interferon-alpha and nucleoside/nucleotide analogs, are only partially effective and new treatment methods remain an important objective. Harnessing the RNA interference (RNAi) pathway to achieve post-transcriptional silencing of rogue genetic elements is an exciting avenue for development of novel therapeutic strategies. The specific and potent suppression of HBV gene expression and replication is an attractive option as a novel and effective approach for the treatment of chronic HBV infection. However, despite significant and rapid progress, existing RNAi technologies require further refinement before clinical applications can be realized. Here, we review current efforts aimed at improving the efficiency of anti-HBV RNAi-based delivery systems, at limiting the toxicities associated with RNAi modalities and at preventing reactivation of viral replication. We discuss the progress towards clinical implementation of anti-HBV RNAi therapies.

摘要

乙型肝炎病毒(HBV)慢性感染发生在全球人口的约 6%,病毒携带者存在肝细胞癌和肝硬化的风险。目前的治疗方案包括干扰素-α和核苷/核苷酸类似物,但仅部分有效,新的治疗方法仍然是一个重要目标。利用 RNA 干扰(RNAi)途径实现流氓遗传元件的转录后沉默,是开发新型治疗策略的一个令人兴奋的途径。特异性和强效抑制 HBV 基因表达和复制是一种有吸引力的选择,作为治疗慢性 HBV 感染的一种新颖而有效的方法。然而,尽管取得了重大而迅速的进展,但现有的 RNAi 技术在临床应用之前还需要进一步改进。在这里,我们综述了目前旨在提高基于 RNAi 的抗 HBV 递药系统效率、限制 RNAi 方式相关毒性以及防止病毒复制再激活的努力。我们讨论了抗 HBV RNAi 疗法向临床实施的进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f44/2873806/11169f8a4f70/gm149-1.jpg

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