The Immunological Conundrum of Endogenous Retroelements.

IF 26.9 1区 医学 Q1 IMMUNOLOGY
George Kassiotis
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引用次数: 8

Abstract

Our defenses against infection rely on the ability of the immune system to distinguish invading pathogens from self. This task is exceptionally challenging, if not seemingly impossible, in the case of retroviruses that have integrated almost seamlessly into the host. This review examines the limits of innate and adaptive immune responses elicited by endogenous retroviruses and other retroelements, the targets of immune recognition, and the consequences for host health and disease. Contrary to theoretical expectation, endogenous retroelements retain substantial immunogenicity, which manifests most profoundly when their epigenetic repression is compromised, contributing to autoinflammatory and autoimmune disease and age-related inflammation. Nevertheless, recent evidence suggests that regulated immune reactivity to endogenous retroelements is integral to immune system development and function, underpinning cancer immunosurveillance, resistance to infection, and responses to the microbiota. Elucidation of the interaction points with endogenous retroelements will therefore deepen our understanding of immune system function and contribution to disease.

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内源性逆转录因子的免疫学难题。
我们对感染的防御依赖于免疫系统区分入侵病原体和自身的能力。对于几乎无缝地整合到宿主体内的逆转录病毒来说,这项任务非常具有挑战性,如果不是看似不可能的话。本文综述了由内源性逆转录病毒和其他逆转录因子引起的先天和适应性免疫反应的局限性,免疫识别的目标,以及对宿主健康和疾病的影响。与理论预期相反,内源性逆转录因子保留了大量的免疫原性,当其表观遗传抑制受到损害时,这种免疫原性表现得最为深刻,从而导致自身炎症和自身免疫性疾病以及与年龄相关的炎症。然而,最近的证据表明,对内源性逆转录因子的调节免疫反应性是免疫系统发育和功能不可或缺的一部分,是癌症免疫监测、感染抵抗和对微生物群反应的基础。因此,阐明与内源性逆转录因子的相互作用点将加深我们对免疫系统功能及其对疾病的贡献的理解。
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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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