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人类致癌 γ 疱疹病毒对巨自噬机制、细胞分化和免疫反应的调控。

Regulation of the Macroautophagic Machinery, Cellular Differentiation, and Immune Responses by Human Oncogenic γ-Herpesviruses.

机构信息

Laboratory of Viral Immunobiology, Institute of Experimental Immunology, University of Zürich, 8057 Zürich, Switzerland.

出版信息

Viruses. 2021 May 8;13(5):859. doi: 10.3390/v13050859.

DOI:10.3390/v13050859
PMID:34066671
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8150893/
Abstract

The human γ-herpesviruses Epstein-Barr virus (EBV) and Kaposi sarcoma-associated herpesvirus (KSHV) encode oncogenes for B cell transformation but are carried by most infected individuals without symptoms. For this purpose, they manipulate the anti-apoptotic pathway macroautophagy, cellular proliferation and apoptosis, as well as immune recognition. The mechanisms and functional relevance of these manipulations are discussed in this review. They allow both viruses to strike the balance between efficient persistence and dissemination in their human hosts without ever being cleared after infection and avoiding pathologies in most of their carriers.

摘要

人类 γ 疱疹病毒 EBV(Epstein-Barr 病毒)和 KSHV(卡波西肉瘤相关疱疹病毒)编码 B 细胞转化的癌基因,但大多数受感染个体无症状携带。为此,它们操纵抗细胞凋亡途径自噬、细胞增殖和凋亡以及免疫识别。本文讨论了这些操作的机制和功能相关性。这些机制使两种病毒能够在不被清除的情况下,在其人类宿主中保持有效的持久性和传播性之间取得平衡,并避免大多数携带者出现病理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aac4/8150893/ab8f4441c9cc/viruses-13-00859-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aac4/8150893/1bbe6e69ad82/viruses-13-00859-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aac4/8150893/ab8f4441c9cc/viruses-13-00859-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aac4/8150893/1bbe6e69ad82/viruses-13-00859-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aac4/8150893/ab8f4441c9cc/viruses-13-00859-g002.jpg

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本文引用的文献

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KSHV infection drives poorly cytotoxic CD56-negative natural killer cell differentiation in vivo upon KSHV/EBV dual infection.在 KSHV/EBV 双重感染时,KSHV 感染可导致体内细胞毒性差的 CD56 阴性自然杀伤细胞分化不良。
Cell Rep. 2021 May 4;35(5):109056. doi: 10.1016/j.celrep.2021.109056.
2
The Epstein-Barr virus deubiquitinase BPLF1 targets SQSTM1/p62 to inhibit selective autophagy.EB 病毒去泛素化酶 BPLF1 靶向 SQSTM1/p62 以抑制选择性自噬。
Autophagy. 2021 Nov;17(11):3461-3474. doi: 10.1080/15548627.2021.1874660. Epub 2021 Jan 28.
3
Viral Infection and Autophagy Dysregulation: The Case of HHV-6, EBV and KSHV.
病毒感染与自噬失调:以 HHV-6、EBV 和 KSHV 为例。
Cells. 2020 Dec 7;9(12):2624. doi: 10.3390/cells9122624.
4
The interplay between EBV and KSHV viral products and NF-κB pathway in oncogenesis.EBV与KSHV病毒产物及NF-κB信号通路在肿瘤发生中的相互作用。
Infect Agent Cancer. 2020 Oct 15;15:62. doi: 10.1186/s13027-020-00317-4. eCollection 2020.
5
Autophagy in Human Diseases.人类疾病中的自噬
N Engl J Med. 2020 Oct 15;383(16):1564-1576. doi: 10.1056/NEJMra2022774.
6
Distinct genetic architectures and environmental factors associate with host response to the γ2-herpesvirus infections.宿主对 γ2-疱疹病毒感染的反应与独特的遗传结构和环境因素有关。
Nat Commun. 2020 Jul 31;11(1):3849. doi: 10.1038/s41467-020-17696-2.
7
Co-infection of Cytomegalovirus and Epstein-Barr Virus Diminishes the Frequency of CD56NKG2AKIR NK Cells and Contributes to Suboptimal Control of EBV in Immunosuppressed Children With Post-transplant Lymphoproliferative Disorder.巨细胞病毒和 Epstein-Barr 病毒合并感染会降低 CD56<sup>NKG2A<sup>KIR<sup>NK 细胞的频率,并导致移植后淋巴组织增生性疾病免疫抑制儿童中 EBV 控制不佳。
Front Immunol. 2020 Jun 17;11:1231. doi: 10.3389/fimmu.2020.01231. eCollection 2020.
8
EBV renders B cells susceptible to HIV-1 in humanized mice.EBV 使人类化小鼠中的 B 细胞易感染 HIV-1。
Life Sci Alliance. 2020 Jun 23;3(8). doi: 10.26508/lsa.202000640. Print 2020 Aug.
9
Autophagy and endocytosis - interconnections and interdependencies.自噬和内吞作用——相互联系和相互依存。
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10
BHRF1, a BCL2 viral homolog, disturbs mitochondrial dynamics and stimulates mitophagy to dampen type I IFN induction.BHRF1,一种 BCL2 病毒同源物,扰乱线粒体动力学并刺激线粒体自噬,以抑制 I 型 IFN 的诱导。
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