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1
The potential impacts of early secreted antigenic target of 6 kDa of Mycobacterium tuberculosis on KSHV-infected cells.结核分枝杆菌早期分泌抗原靶 6kDa 对感染 KSHV 细胞的潜在影响。
J Med Virol. 2021 Jun;93(6):4028-4032. doi: 10.1002/jmv.26291. Epub 2020 Jul 17.
2
Kaposi's Sarcoma-Associated Herpesvirus Infection Induces the Expression of Neuroendocrine Genes in Endothelial Cells.卡波西肉瘤相关疱疹病毒感染诱导内皮细胞中神经内分泌基因的表达。
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HIV-1 Tat Interacts with a Kaposi's Sarcoma-Associated Herpesvirus Reactivation-Upregulated Antiangiogenic Long Noncoding RNA, LINC00313, and Antagonizes Its Function.HIV-1 Tat 与卡波西肉瘤相关疱疹病毒再激活上调的抗血管生成长非编码 RNA LINC00313 相互作用,并拮抗其功能。
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Glycolysis, Glutaminolysis, and Fatty Acid Synthesis Are Required for Distinct Stages of Kaposi's Sarcoma-Associated Herpesvirus Lytic Replication.卡波西肉瘤相关疱疹病毒裂解复制的不同阶段需要糖酵解、谷氨酰胺分解和脂肪酸合成。
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HIV-1 infection of primary effusion lymphoma cell line triggers Kaposi's sarcoma-associated herpesvirus (KSHV) reactivation.原发性渗出性淋巴瘤细胞系的HIV-1感染引发卡波西肉瘤相关疱疹病毒(KSHV)再激活。
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Expression and Subcellular Localization of the Kaposi's Sarcoma-Associated Herpesvirus K15P Protein during Latency and Lytic Reactivation in Primary Effusion Lymphoma Cells.卡波西肉瘤相关疱疹病毒K15P蛋白在原发性渗出性淋巴瘤细胞潜伏和裂解再激活过程中的表达及亚细胞定位
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Inhibition of KAP1 enhances hypoxia-induced Kaposi's sarcoma-associated herpesvirus reactivation through RBP-Jκ.抑制 KAP1 通过 RBP-Jκ 增强缺氧诱导的卡波西肉瘤相关疱疹病毒再激活。
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Human immunodeficiency virus type-1 activates lytic cycle replication of Kaposi's sarcoma-associated herpesvirus through induction of KSHV Rta.1型人类免疫缺陷病毒通过诱导卡波西肉瘤相关疱疹病毒Rta激活其裂解周期复制。
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引用本文的文献

1
The Impact of Co-Infections for Human Gammaherpesvirus Infection and Associated Pathologies.人类γ疱疹病毒感染及其相关疾病的合并感染的影响。
Int J Mol Sci. 2023 Aug 22;24(17):13066. doi: 10.3390/ijms241713066.
2
Regulation of KSHV Latency and Lytic Reactivation.调控卡波氏肉瘤相关疱疹病毒潜伏和裂解性再激活。
Viruses. 2020 Sep 17;12(9):1034. doi: 10.3390/v12091034.

结核分枝杆菌早期分泌抗原靶 6kDa 对感染 KSHV 细胞的潜在影响。

The potential impacts of early secreted antigenic target of 6 kDa of Mycobacterium tuberculosis on KSHV-infected cells.

机构信息

Department of Pathology, University of Arkansas for Medical Sciences, Little Rock, Arkansas.

Department of Pulmonary Immunology, University of Texas Health Science Center, Tyler, Texas.

出版信息

J Med Virol. 2021 Jun;93(6):4028-4032. doi: 10.1002/jmv.26291. Epub 2020 Jul 17.

DOI:10.1002/jmv.26291
PMID:32648938
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7796979/
Abstract

Kaposi's sarcoma-associated herpesvirus (KSHV) causes several human cancers, including Kaposi's sarcoma (KS) and primary effusion lymphoma, which are mostly seen in immunocompromised patients, such as human immunodefeciency virus (HIV)+ individuals. Tuberculosis (TB), caused by the bacterial pathogen Mycobacterium tuberculosis (Mtb), remains one of the deadliest infectious diseases in the world. The risk of developing TB is dramatically higher in people living with HIV than among those without HIV infection. Case reports link cutaneous or pulmonary KS in HIV+ patients with mycobacterial co-infections, however, impacts of Mtb infection or its products on KSHV-infected cells are not known. We report here that ESAT-6, a secreted Mtb virulence factor, induces viral reactivation from KSHV-infected cells. KSHV-infected pulmonary endothelial cells were resistant to ESAT-6 induced inhibition of cell growth. Our data demonstrate that Mtb virulence factors influence the biology of KSHV-infected cells, highlighting the need to study the interactions between these two pathogens commonly found in people living with HIV.

摘要

卡波济肉瘤相关疱疹病毒(KSHV)可引起几种人类癌症,包括卡波济肉瘤(KS)和原发性渗出性淋巴瘤,这些癌症主要发生在免疫功能低下的患者中,如人类免疫缺陷病毒(HIV)+个体。由细菌病原体结核分枝杆菌(Mtb)引起的结核病仍然是世界上最致命的传染病之一。与未感染 HIV 的人相比,HIV 感染者患结核病的风险要高得多。病例报告将 HIV+患者的皮肤或肺部 KS 与分枝杆菌合并感染联系起来,然而,尚不清楚 Mtb 感染或其产物对感染 KSHV 的细胞的影响。我们在这里报告,ESAT-6,一种分泌型 Mtb 毒力因子,可诱导 KSHV 感染细胞的病毒重新激活。感染 KSHV 的肺内皮细胞对 ESAT-6 诱导的细胞生长抑制具有抗性。我们的数据表明,Mtb 毒力因子影响感染 KSHV 的细胞的生物学特性,突出了需要研究这两种常见于 HIV 感染者的病原体之间的相互作用。