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轮状病毒感染抗病毒药物的研发进展。

Advances in the development of antivirals for rotavirus infection.

作者信息

Jiang Lin, Tang Ao, Song Lihua, Tong Yigang, Fan Huahao

机构信息

College of Life Science and Technology, Beijing University of Chemical Technology, Beijing, China.

出版信息

Front Immunol. 2023 Mar 17;14:1041149. doi: 10.3389/fimmu.2023.1041149. eCollection 2023.

DOI:10.3389/fimmu.2023.1041149
PMID:37006293
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10063883/
Abstract

Rotavirus (RV) causes 200,000 deaths per year and imposes a serious burden to public health and livestock farming worldwide. Currently, rehydration (oral and intravenous) remains the main strategy for the treatment of rotavirus gastroenteritis (RVGE), and no specific drugs are available. This review discusses the viral replication cycle in detail and outlines possible therapeutic approaches including immunotherapy, probiotic-assisted therapy, anti-enteric secretory drugs, Chinese medicine, and natural compounds. We present the latest advances in the field of rotavirus antivirals and highlights the potential use of Chinese medicine and natural compounds as therapeutic agents. This review provides an important reference for rotavirus prevention and treatment.

摘要

轮状病毒(RV)每年导致20万人死亡,给全球公共卫生和畜牧业带来沉重负担。目前,补液(口服和静脉注射)仍然是治疗轮状病毒胃肠炎(RVGE)的主要策略,且尚无特效药物。本综述详细讨论了病毒复制周期,并概述了可能的治疗方法,包括免疫疗法、益生菌辅助疗法、抗肠道分泌药物、中药和天然化合物。我们介绍了轮状病毒抗病毒药物领域的最新进展,并强调了中药和天然化合物作为治疗剂的潜在用途。本综述为轮状病毒的预防和治疗提供了重要参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d37/10063883/b69f29626cad/fimmu-14-1041149-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d37/10063883/758877d142b9/fimmu-14-1041149-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d37/10063883/912f0b734ff8/fimmu-14-1041149-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d37/10063883/35ed009824f8/fimmu-14-1041149-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d37/10063883/b69f29626cad/fimmu-14-1041149-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d37/10063883/758877d142b9/fimmu-14-1041149-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d37/10063883/912f0b734ff8/fimmu-14-1041149-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d37/10063883/35ed009824f8/fimmu-14-1041149-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d37/10063883/b69f29626cad/fimmu-14-1041149-g004.jpg

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Front Cell Infect Microbiol. 2022 Mar 29;12:854989. doi: 10.3389/fcimb.2022.854989. eCollection 2022.
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Rotavirus-Mediated Prostaglandin E Production in MA104 Cells Promotes Virus Attachment and Internalisation, Resulting in an Increased Viral Load.
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Immunoinformatics-driven design of a multi-epitope vaccine targeting neonatal rotavirus with focus on outer capsid proteins VP4 and VP7 and non structural proteins NSP2 and NSP5.免疫信息学驱动的针对新生儿轮状病毒的多表位疫苗设计,重点关注外衣壳蛋白VP4和VP7以及非结构蛋白NSP2和NSP5。
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