Suppr超能文献

Ⅰ型干扰素病:10 年进展。

The type I interferonopathies: 10 years on.

机构信息

MRC Human Genetics Unit, Institute of Genetics and Cancer, University of Edinburgh, Edinburgh, UK.

Laboratory of Neurogenetics and Neuroinflammation, Institut Imagine, Université de Paris, Paris, France.

出版信息

Nat Rev Immunol. 2022 Aug;22(8):471-483. doi: 10.1038/s41577-021-00633-9. Epub 2021 Oct 20.

Abstract

As brutally demonstrated by the COVID-19 pandemic, an effective immune system is essential for survival. Developed over evolutionary time, viral nucleic acid detection is a central pillar in the defensive armamentarium used to combat foreign microbial invasion. To ensure cellular homeostasis, such a strategy necessitates the efficient discrimination of pathogen-derived DNA and RNA from that of the host. In 2011, it was suggested that an upregulation of type I interferon signalling might serve as a defining feature of a novel set of Mendelian inborn errors of immunity, where antiviral sensors are triggered by host nucleic acids due to a failure of self versus non-self discrimination. These rare disorders have played a surprisingly significant role in informing our understanding of innate immunity and the relevance of type I interferon signalling for human health and disease. Here we consider what we have learned in this time, and how the field may develop in the future.

摘要

正如 COVID-19 大流行所残酷展示的那样,有效的免疫系统对于生存至关重要。病毒核酸检测是经过进化时间发展起来的,是用于对抗外来微生物入侵的防御武器库中的核心支柱。为了确保细胞内环境稳定,这种策略需要有效地将病原体来源的 DNA 和 RNA 与宿主的 DNA 和 RNA 区分开来。2011 年,有人提出,I 型干扰素信号的上调可能是一组新的孟德尔遗传性免疫缺陷的特征,其中由于自我与非自我的区分失败,抗病毒传感器会被宿主的核酸触发。这些罕见的疾病在告知我们对先天免疫的理解以及 I 型干扰素信号对人类健康和疾病的相关性方面发挥了惊人的重要作用。在这里,我们考虑在此期间所学到的内容,以及该领域未来可能的发展方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6287/8527296/455f50aaca06/41577_2021_633_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验