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丙型肝炎病毒与分子模拟

Hepatitis C Virus and Molecular Mimicry.

作者信息

Goh Lynette, Kerkar Nanda

机构信息

KK Women's and Children's Hospital, Singapore 229899, Singapore.

Massachusetts General Hospital for Children, Harvard Medical School, Boston, MA 02114, USA.

出版信息

Pathogens. 2024 Jun 22;13(7):527. doi: 10.3390/pathogens13070527.

DOI:10.3390/pathogens13070527
PMID:39057754
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11280050/
Abstract

This review delves into the interactions between hepatitis C virus (HCV) and the host immune system, shedding light on how by using the mechanism of molecular mimicry, the virus strategically evades the immune system, resulting in a cascade of diverse complications. HCV, notorious for its ability to persistently infect hepatocytes, employs molecular mimicry to resemble host proteins, thereby avoiding immune detection and mounting an effective defense. This mimicry also triggers systemic autoimmune responses that lead to various sequelae. The objective of this review is to comprehensively explore the role of HCV-induced molecular mimicry, which not only facilitates viral survival but is also instrumental in developing autoimmune and inflammatory disorders. By mimicking host proteins, HCV triggers an immune response that inadvertently attacks the host, fostering the development of autoimmune and other inflammatory disorders. Understanding the nuanced mechanisms of HCV-mediated molecular mimicry provides crucial insights into the multifaceted sequelae of viral infections on host immune responses. Unravelling these complexities is paramount for advancing therapeutic strategies that not only target the virus directly but also mitigate the secondary autoimmune and inflammatory complications induced by HCV.

摘要

本综述深入探讨了丙型肝炎病毒(HCV)与宿主免疫系统之间的相互作用,揭示了该病毒如何通过分子模拟机制巧妙地逃避免疫系统,从而引发一系列复杂的并发症。HCV以其持续感染肝细胞的能力而臭名昭著,它利用分子模拟来模仿宿主蛋白,进而逃避免疫检测并建立有效的防御机制。这种模拟还会引发全身性自身免疫反应,导致各种后遗症。本综述的目的是全面探讨HCV诱导的分子模拟的作用,这不仅有助于病毒存活,还在自身免疫性疾病和炎症性疾病的发展中发挥重要作用。通过模仿宿主蛋白,HCV引发的免疫反应会不经意地攻击宿主,促进自身免疫性疾病和其他炎症性疾病的发展。了解HCV介导的分子模拟的细微机制,对于深入了解病毒感染对宿主免疫反应产生的多方面后遗症至关重要。揭示这些复杂性对于推进治疗策略至关重要,这些策略不仅要直接靶向病毒,还要减轻HCV引发的继发性自身免疫和炎症并发症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c4a/11280050/3a27427d67c3/pathogens-13-00527-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c4a/11280050/c9fc62d7cd00/pathogens-13-00527-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c4a/11280050/3a27427d67c3/pathogens-13-00527-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c4a/11280050/c9fc62d7cd00/pathogens-13-00527-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c4a/11280050/3a27427d67c3/pathogens-13-00527-g002.jpg

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World J Hepatol. 2024 Feb 27;16(2):286-293. doi: 10.4254/wjh.v16.i2.286.
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Autoimmune and autoinflammatory conditions after COVID-19 vaccination. New case reports and updated literature review.接种 COVID-19 疫苗后的自身免疫和自身炎症性疾病。新病例报告和最新文献回顾。
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Persistent Autoimmune Activation and Proinflammatory State in Post-Coronavirus Disease 2019 Syndrome.
新冠病毒感染后综合征中持续的自身免疫激活和促炎状态。
J Infect Dis. 2022 Jun 15;225(12):2155-2162. doi: 10.1093/infdis/jiac017.
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New Onset of Autoimmune Diseases Following COVID-19 Diagnosis.新冠病毒感染后自身免疫性疾病的新发病例。
Cells. 2021 Dec 20;10(12):3592. doi: 10.3390/cells10123592.
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New-onset IgG autoantibodies in hospitalized patients with COVID-19.新型冠状病毒肺炎住院患者新出现的IgG自身抗体
Nat Commun. 2021 Sep 14;12(1):5417. doi: 10.1038/s41467-021-25509-3.
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Treatment of chronic hepatitis C-associated cryoglobulinemia vasculitis at the era of direct-acting antivirals.直接作用抗病毒药物时代慢性丙型肝炎相关冷球蛋白血症性血管炎的治疗
Therap Adv Gastroenterol. 2020 Jul 24;13:1756284820942617. doi: 10.1177/1756284820942617. eCollection 2020.
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