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人内源性逆转录病毒、免疫与自身免疫:理解它们之间的联系

HERVs, immunity, and autoimmunity: understanding the connection.

作者信息

Greenig Matthew

机构信息

Department of Life Sciences, Imperial College London, London, United Kingdom.

出版信息

PeerJ. 2019 Apr 5;7:e6711. doi: 10.7717/peerj.6711. eCollection 2019.

DOI:10.7717/peerj.6711
PMID:30984482
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6452852/
Abstract

Since their discovery in the 1960s, further investigation into endogenous retroviruses (ERVs) has challenged the conventional view of viral sequences as exclusively parasitic elements. Once presumed to be a group of passive genetic relics, it is becoming increasingly clear that this view of ERVs, while generally accurate, is incorrect in many specific cases. Research has identified ERV genes that appear to be co-opted by their mammalian hosts, but the biological function of ERV elements in humans remains a controversial subject. One area that has attracted some attention in this domain is the role of co-opted ERV elements in mammalian immune systems. The relationship between ERVs and human autoimmune diseases has also been investigated, but has historically been treated as a separate topic. This review will summarize the current evidence concerning the phenotypic significance of ERVs, both in the healthy immune system and in manifestations of autoimmunity. Furthermore, it will evaluate the relationship between these fields of study, and propose previously-unexplored molecular mechanisms through which human endogenous retroviruses might contribute to certain autoimmune pathologies. Investigation into these novel mechanisms could further our understanding of the molecular basis of autoimmune disease, and may one day provide new targets for treatment.

摘要

自20世纪60年代内源性逆转录病毒(ERVs)被发现以来,对其进一步的研究挑战了病毒序列仅是寄生元件的传统观点。ERVs曾经被认为是一组被动的遗传遗迹,现在越来越清楚的是,这种对ERVs的看法虽然总体上是准确的,但在许多具体情况下是不正确的。研究已经确定了一些似乎被其哺乳动物宿主所征用的ERV基因,但ERV元件在人类中的生物学功能仍然是一个有争议的话题。在这一领域引起一些关注的一个方面是被征用的ERV元件在哺乳动物免疫系统中的作用。ERVs与人类自身免疫性疾病之间的关系也已得到研究,但在历史上一直被视为一个单独的话题。本综述将总结当前关于ERVs在健康免疫系统和自身免疫表现中的表型意义的证据。此外,它将评估这些研究领域之间的关系,并提出人类内源性逆转录病毒可能导致某些自身免疫性病理的前所未有的分子机制。对这些新机制的研究可以加深我们对自身免疫性疾病分子基础的理解,也许有一天会提供新的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7470/6452852/20a6648eb6ff/peerj-07-6711-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7470/6452852/8378b9b39532/peerj-07-6711-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7470/6452852/1279ddafaf48/peerj-07-6711-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7470/6452852/a62133eab51c/peerj-07-6711-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7470/6452852/0499c6222b74/peerj-07-6711-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7470/6452852/20a6648eb6ff/peerj-07-6711-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7470/6452852/8378b9b39532/peerj-07-6711-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7470/6452852/1279ddafaf48/peerj-07-6711-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7470/6452852/a62133eab51c/peerj-07-6711-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7470/6452852/0499c6222b74/peerj-07-6711-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7470/6452852/20a6648eb6ff/peerj-07-6711-g005.jpg

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