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在动物中模拟 HCV 疾病:HCV 和 GBV-B 感染的病毒学、免疫学和发病机制。

Modeling HCV disease in animals: virology, immunology and pathogenesis of HCV and GBV-B infections.

机构信息

Center for Virology and Vaccine Research, Beth Israel Deaconess Medical Center - Harvard Medical School Boston, MA, USA.

出版信息

Front Microbiol. 2014 Dec 8;5:690. doi: 10.3389/fmicb.2014.00690. eCollection 2014.

Abstract

Hepatitis C virus (HCV) infection has become a global public health burden costing billions of dollars in health care annually. Even with rapidly advancing scientific technologies this disease still poses a significant threat due to a lack of vaccines and affordable treatment options. The immune correlates of protection and predisposing factors toward chronicity remain major obstacles to development of HCV vaccines and immunotherapeutics due, at least in part, to lack of a tangible infection animal model. This review discusses the currently available animal models for HCV disease with a primary focus on GB virus B (GBV-B) infection of New World primates that recapitulates the dual Hepacivirus phenotypes of acute viral clearance and chronic pathologic disease. HCV and GBV-B are also closely phylogenetically related and advances in characterization of the immune systems of New World primates have already led to the use of this model for drug testing and vaccine trials. Herein, we discuss the benefits and caveats of the GBV-B infection model and discuss potential avenues for future development of novel vaccines and immunotherapies.

摘要

丙型肝炎病毒 (HCV) 感染已成为全球公共卫生负担,每年在医疗保健方面耗资数十亿美元。尽管科学技术飞速发展,但由于缺乏疫苗和负担得起的治疗方案,这种疾病仍然构成重大威胁。由于缺乏有形的感染动物模型,保护的免疫相关性和慢性发生的诱发因素仍然是 HCV 疫苗和免疫疗法发展的主要障碍。本文讨论了目前用于 HCV 疾病的动物模型,主要集中在新世界灵长类动物的 GB 病毒 B (GBV-B) 感染上,该模型重现了急性病毒清除和慢性病理疾病的双重嗜肝病毒表型。HCV 和 GBV-B 也具有密切的系统发育关系,对新世界灵长类动物免疫系统的特征的研究进展已经导致该模型被用于药物测试和疫苗试验。在此,我们讨论了 GBV-B 感染模型的优缺点,并讨论了开发新型疫苗和免疫疗法的潜在途径。

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