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慢性丙型肝炎感染期间和之后的 HCV 特异性 T 细胞应答。

HCV-Specific T Cell Responses During and After Chronic HCV Infection.

机构信息

Department of Medicine II, Medical Center-University of Freiburg, Faculty of Medicine, University of Freiburg, 79106 Freiburg, Germany.

出版信息

Viruses. 2018 Nov 17;10(11):645. doi: 10.3390/v10110645.

Abstract

Hepatitis C virus (HCV)-specific T cell responses are closely linked to the clinical course of infection. While T cell responses in self-limiting infection are typically broad and multi-specific, they display several distinct features of functional impairment in the chronic phase. Moreover, HCV readily adapts to immune pressure by developing escape mutations within epitopes targeted by T cells. Much of our current knowledge on HCV-specific T cell responses has been gathered under the assumption that this might eventually pave the way for a therapeutic vaccine. However, with the development of highly efficient direct acting antivirals (DAAs), there is less interest in the development of a therapeutic vaccine for HCV and the scope of T cell research has shifted. Indeed, the possibility to rapidly eradicate an antigen that has persisted over years or decades, and has led to T cell exhaustion and dysfunction, provides the unique opportunity to study potential T cell recovery after antigen cessation in a human in vivo setting. Findings from such studies not only improve our basic understanding of T cell immunity but may also advance immunotherapeutic approaches in cancer or chronic hepatitis B and D infection. Moreover, in order to edge closer to the WHO goal of HCV elimination by 2030, a prophylactic vaccine is clearly required. Thus, in this review, we will summarize our current knowledge on HCV-specific T cell responses and also provide an outlook on the open questions that require answers in this field.

摘要

丙型肝炎病毒 (HCV) 特异性 T 细胞应答与感染的临床过程密切相关。虽然自限性感染中的 T 细胞应答通常广泛且多特异性,但在慢性期它们表现出几种功能受损的明显特征。此外,HCV 通过在 T 细胞靶向的表位中产生逃逸突变,很容易适应免疫压力。我们目前对 HCV 特异性 T 细胞应答的了解很大程度上是基于这样一种假设,即这可能最终为治疗性疫苗铺平道路。然而,随着高效直接作用抗病毒药物 (DAA) 的发展,对 HCV 治疗性疫苗的开发兴趣降低,T 细胞研究的范围也发生了转移。事实上,迅速消除抗原的可能性为研究抗原停止后人类体内 T 细胞恢复的潜力提供了独特的机会,该抗原已经持续存在多年或几十年,并导致 T 细胞衰竭和功能障碍。这些研究的结果不仅提高了我们对 T 细胞免疫的基本认识,而且可能也推进了癌症或慢性乙型和丙型肝炎感染的免疫治疗方法。此外,为了更接近世卫组织到 2030 年消除 HCV 的目标,显然需要预防性疫苗。因此,在这篇综述中,我们将总结我们目前对 HCV 特异性 T 细胞应答的认识,并对该领域需要回答的开放性问题进行展望。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7246/6265781/ca8f2df3b5c8/viruses-10-00645-g001.jpg

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