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1型人类免疫缺陷病毒(HIV-1)与1型人类嗜T淋巴细胞病毒(HTLV-I)在体外培养的单核细胞衍生巨噬细胞中的差异相互作用模式:对HIV-1与HTLV-I体内合并感染的影响

Differential patterns of interaction between HIV type 1 and HTLV type I in monocyte-derived macrophages cultured in vitro: implications for in vivo coinfection with HIV type 1 and HTLV type I.

作者信息

Szabó J, Beck Z, Csomán E, Liu X, Andrikó I, Kiss J, Bácsi A, Ebbesen P, Tóth F D

机构信息

Institute of Microbiology, University Medical School, Debrecen, Hungary.

出版信息

AIDS Res Hum Retroviruses. 1999 Dec 10;15(18):1653-66. doi: 10.1089/088922299309694.

Abstract

The interaction between human immunodeficiency virus type 1 (HIV-1) and human T cell leukemia-lymphoma virus type I (HTLV-I) has generated substantial interest. However, there is disagreement on the in vivo consequences of the double infection. We investigated the interactions between HIV-1 and HTLV-I in monocyte-derived macrophages cultured in vitro. For study, the T cell-tropic strain IIIB and the macrophagetropic strain Ada-M of HIV-1 were used. The HTLV-I was prepared from the supernatants of the virus-producing MT-2 cell line. We found that coinfection of macrophages with T cell-tropic HIV-1 and HTLV-I significantly enhanced HIV-1 replication, whereas double infection of the cells with macrophage-tropic HIV-1 and HTLV-I resulted in marked upregulation of HTLV-I production. Stimulatory interactions between HIV-1 and HTLV-I were mediated by their trans-acting proteins. Results of study on nuclear translocation of proviral DNA showed that the tax gene product of HTLV-I was able to facilitate the nuclear import of the reverse-transcribed HIV-1(IIIB) DNA. In contrast, the HIV-1 Tat protein did not increase the intranuclear trafficking of HTLV-I DNA, which suggests another mechanism for HTLV-I enhancement by the tat gene product. In conclusion, this study provides possible mechanisms whereby coinfection of an individual with HIV-1 and HTLV-I may influence the clinical outcome of double infection.

摘要

1型人类免疫缺陷病毒(HIV-1)与I型人类T细胞白血病淋巴瘤病毒(HTLV-I)之间的相互作用引发了广泛关注。然而,对于双重感染在体内的后果存在分歧。我们在体外培养的单核细胞衍生巨噬细胞中研究了HIV-1与HTLV-I之间的相互作用。为了进行研究,使用了HIV-1的T细胞嗜性菌株IIIB和巨噬细胞嗜性菌株Ada-M。HTLV-I是从产生病毒的MT-2细胞系的上清液中制备的。我们发现,巨噬细胞被T细胞嗜性HIV-1和HTLV-I共同感染会显著增强HIV-1的复制,而细胞被巨噬细胞嗜性HIV-1和HTLV-I双重感染则会导致HTLV-I产生明显上调。HIV-1与HTLV-I之间的刺激相互作用是由它们的反式作用蛋白介导的。对前病毒DNA核转运的研究结果表明,HTLV-I的tax基因产物能够促进逆转录的HIV-1(IIIB)DNA的核输入。相反,HIV-1的Tat蛋白并没有增加HTLV-I DNA的核内运输,这提示了tat基因产物增强HTLV-I的另一种机制。总之,本研究提供了个体被HIV-1和HTLV-I双重感染可能影响双重感染临床结果的潜在机制。

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