人类对eb病毒的免疫反应由免疫缺陷引起。

IF 26.9 1区 医学 Q1 IMMUNOLOGY
Sylvain Latour
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引用次数: 0

摘要

先天免疫错误(IEIs)在揭示人类免疫的关键组成部分的自然模型中是独特的,特别是那些易受感染的组成部分。eb病毒(EBV)是人类最常见的机会性感染因子之一,可导致多种疾病,包括传染性单核细胞增多症、非恶性和恶性淋巴细胞增生性疾病、噬血细胞性淋巴组织细胞增多症、平滑肌和上皮肿瘤。对大多数人来说,EBV感染会持续一生,没有病理后果。不容易感染eb病毒的iei表明,先天和体液反应对于eb病毒的免疫反应不是必要的或多余的。IEIs与EBV感染的高易感性相关,这为CD8+ T细胞反应在EBV免疫中发挥核心作用提供了明确的遗传学证据。他们还强调了不同的步骤和途径,一方面,CD8+ T细胞的效应细胞毒性功能,另一方面,细胞毒性CD8+ T细胞的扩增和成熟。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Human Immune Responses to Epstein-Barr Virus Highlighted by Immunodeficiencies.

Inborn errors of immunity (IEIs) represent unique in natura models that uncover key components of immunity in humans, in particular those that predispose to infections. Epstein-Barr virus (EBV) is one of the most common opportunistic infectious agents in humans and is responsible for several diseases, including infectious mononucleosis, nonmalignant and malignant lymphoproliferative disorders, hemophagocytic lymphohistiocytosis, and smooth muscle and epithelial tumors. For most individuals, EBV infection persists for life without pathological consequences. IEIs that do not predispose to EBV infection suggest that innate and humoral responses are not necessary or redundant for the immune response to EBV. IEIs associated with high susceptibility to EBV infection provide unequivocal genetic proof of the central role of CD8+ T cell responses in immunity to EBV. They also highlight the distinct steps and pathways required for, on the one hand, the effector cytotoxic functions of CD8+ T cells and, on the other hand, the expansion and maturation of cytotoxic CD8+ T cells.

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来源期刊
Annual review of immunology
Annual review of immunology 医学-免疫学
CiteScore
57.20
自引率
0.70%
发文量
29
期刊介绍: The Annual Review of Immunology, in publication since 1983, focuses on basic immune mechanisms and molecular basis of immune diseases in humans. Topics include innate and adaptive immunity; immune cell development and differentiation; immune control of pathogens (viruses, bacteria, parasites) and cancer; and human immunodeficiency and autoimmune diseases. The current volume of this journal has been converted from gated to open access through Annual Reviews' Subscribe to Open program, with all articles published under a CC BY license.
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