EBV的先天免疫识别。

3区 医学 Q2 Medicine
Jessica Stewart, Blossom Damania
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引用次数: 0

摘要

eb病毒(EBV)是一种非常成功的人类病原体,全球血清患病率约为95% (Mentzer et al, Nat comm 13:1818, 2022)。如果在儿童早期感染,eb病毒感染通常是无症状的;然而,青少年和成年期的感染可表现为传染性单核细胞增多症(IM)。先天免疫反应是第一道防线,其功能对控制EBV感染至关重要。在EBV感染期间,被称为病原体相关分子模式(pamp)的病毒成分被种系编码模式识别受体(PRRs)识别。PRRs存在于非免疫细胞和免疫细胞中,包括抗原呈递细胞,如巨噬细胞、单核细胞、树突状细胞、自然杀伤细胞(NK)和肥大细胞。在eb病毒感染的主要目标B细胞和上皮细胞上也发现了PRRs。在没有免疫监视的情况下,EBV可以转化细胞诱导各种恶性肿瘤。相反,长期的先天免疫反应会导致慢性炎症,从而增加患癌症的可能性。本文就eb病毒及其相关疾病的先天免疫识别作一综述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Innate Immune Recognition of EBV.

Epstein-Barr virus (EBV) is a very successful human pathogen, with ~95% seroprevalence worldwide (Mentzer et al, Nat Commun 13:1818, 2022). If contracted in early childhood, EBV infection is typically asymptomatic; however, infections in adolescence and adulthood can manifest as infectious mononucleosis (IM). The innate immune response is the first line of defense, and its function is critical for controlling EBV infection. During EBV infection, components of the virus, known as pathogen-associated molecular patterns (PAMPs), are recognized by germline-encoded pattern recognition receptors (PRRs). PRRs are found on both non-immune and immune cells including antigen-presenting cells, such as macrophages, monocytes, dendritic cells, natural killer (NK), and mast cells. PRRs are also found on B cells and epithelial cells, the primary targets of EBV infection. Without immune surveillance, EBV can transform cells inducing various malignancies. Conversely, a prolonged innate immune response can lead to chronic inflammation which increases the likelihood of cancer. This review discusses innate immune recognition of EBV and its associated diseases.

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来源期刊
CiteScore
5.60
自引率
0.00%
发文量
26
审稿时长
>12 weeks
期刊介绍: The review series Current Topics in Microbiology and Immunology provides a synthesis of the latest research findings in the areas of molecular immunology, bacteriology and virology. Each timely volume contains a wealth of information on the featured subject. This review series is designed to provide access to up-to-date, often previously unpublished information.
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