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组织中巨细胞病毒的免疫监视。

Immune surveillance of cytomegalovirus in tissues.

机构信息

Center for Proteomics, Faculty of Medicine, University of Rijeka, Rijeka, Croatia.

Department of Biomedical Sciences, Croatian Academy of Sciences and Arts, Rijeka, Croatia.

出版信息

Cell Mol Immunol. 2024 Sep;21(9):959-981. doi: 10.1038/s41423-024-01186-2. Epub 2024 Aug 12.

DOI:10.1038/s41423-024-01186-2
PMID:39134803
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11364667/
Abstract

Cytomegalovirus (CMV), a representative member of the Betaherpesvirinae subfamily of herpesviruses, is common in the human population, but immunocompetent individuals are generally asymptomatic when infected with this virus. However, in immunocompromised individuals and immunologically immature fetuses and newborns, CMV can cause a wide range of often long-lasting morbidities and even death. CMV is not only widespread throughout the population but it is also widespread in its hosts, infecting and establishing latency in nearly all tissues and organs. Thus, understanding the pathogenesis of and immune responses to this virus is a prerequisite for developing effective prevention and treatment strategies. Multiple arms of the immune system are engaged to contain the infection, and general concepts of immune control of CMV are now reasonably well understood. Nonetheless, in recent years, tissue-specific immune responses have emerged as an essential factor for resolving CMV infection. As tissues differ in biology and function, so do immune responses to CMV and pathological processes during infection. This review discusses state-of-the-art knowledge of the immune response to CMV infection in tissues, with particular emphasis on several well-studied and most commonly affected organs.

摘要

巨细胞病毒(CMV)是疱疹病毒β亚科的代表性成员,在人群中很常见,但免疫功能正常的个体感染该病毒时通常无症状。然而,在免疫功能低下的个体以及免疫不成熟的胎儿和新生儿中,CMV 可引起广泛的、常为持久的病态甚至死亡。CMV 不仅在人群中广泛存在,而且在其宿主中也广泛存在,几乎感染和潜伏在所有组织和器官中。因此,了解该病毒的发病机制和免疫反应是制定有效预防和治疗策略的前提。免疫系统的多个分支参与控制感染,目前对 CMV 的免疫控制的一般概念有了相当的理解。尽管如此,近年来,组织特异性免疫反应已成为解决 CMV 感染的一个重要因素。由于组织在生物学和功能上存在差异,因此对 CMV 的免疫反应以及感染过程中的病理过程也存在差异。本综述讨论了组织中针对 CMV 感染的免疫反应的最新知识,特别强调了几个研究较多和最常受影响的器官。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfc0/11364667/f1ba4815e13f/41423_2024_1186_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfc0/11364667/a8946eaf2723/41423_2024_1186_Fig1_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfc0/11364667/f1ba4815e13f/41423_2024_1186_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfc0/11364667/a8946eaf2723/41423_2024_1186_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfc0/11364667/92358497588d/41423_2024_1186_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfc0/11364667/dd2965b4ff26/41423_2024_1186_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfc0/11364667/3e8e5f0dce06/41423_2024_1186_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfc0/11364667/f1ba4815e13f/41423_2024_1186_Fig5_HTML.jpg

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Decidual-tissue-resident memory T cells protect against nonprimary human cytomegalovirus infection at the maternal-fetal interface.蜕膜组织驻留记忆 T 细胞可在母体-胎儿界面预防非原发性人巨细胞病毒感染。
Cell Rep. 2024 Feb 27;43(2):113698. doi: 10.1016/j.celrep.2024.113698. Epub 2024 Jan 23.
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Late-rising CD4 T cells resolve mouse cytomegalovirus persistent replication in the salivary gland.
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Viruses. 2025 May 14;17(5):705. doi: 10.3390/v17050705.
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Clinical presentation of cytomegalovirus meningoencephalitis: a retrospective study of 12 adult patients with a variety of immunocompromised conditions.巨细胞病毒性脑膜脑炎的临床表现:对12例患有各种免疫功能低下疾病的成年患者的回顾性研究。
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