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人类嗜T淋巴细胞病毒I型(HTLV-I)致癌作用:成人T细胞白血病/淋巴瘤(ATL)发病机制中病毒与宿主相互作用的分子层面

Human T Lymphotropic Virus Type I (HTLV-I) Oncogenesis: Molecular Aspects of Virus and Host Interactions in Pathogenesis of Adult T cell Leukemia/Lymphoma (ATL).

作者信息

Ahmadi Ghezeldasht Sanaz, Shirdel Abbas, Assarehzadegan Mohammad Ali, Hassannia Tahereh, Rahimi Hosian, Miri Rahele, Rezaee S A Rahim

机构信息

Research Centre for HIV/AIDS, HTLV and Viral Hepatitis, Iranian Academic Centre for Education, Culture & Research (ACECR), Mashhad Branch, Mashhad, Iran.

Inflammation and Inflammatory diseases research Centre, Medical School, Mashhad University of Medical Science, Mashhad, Iran.

出版信息

Iran J Basic Med Sci. 2013 Mar;16(3):179-95.

PMID:24470860
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3881257/
Abstract

The study of tumor viruses paves the way for understanding the mechanisms of virus pathogenesis, including those involved in establishing infection and dissemination in the host tumor affecting immune-compromised patients. The processes ranging from viral infection to progressing malignancy are slow and usually insufficient for establishment of transformed cells that develop cancer in only a minority of infected subjects. Therefore, viral infection is usually not the only cause of cancer, and further environmental and host factors, may be implicated. HTLV-I, in particular, is considered as an oncovirus cause of lymphoproliferative disease such as adult T cell leukemia/lymphoma (ATL) and disturbs the immune responses which results in HTLV-I associated meylopathy/tropical spastic parapresis (HAM/TSP). HTLV-I infection causes ATL in a small proportion of infected subjects (2-5%) following a prolonged incubation period (15-30 years) despite a strong adaptive immune response against the virus. Overall, these conditions offer a prospect to study the molecular basis of tumorgenicity in mammalian cells. In this review, the oncogencity of HTLV-I is being considered as an oncovirus in context of ATL.

摘要

肿瘤病毒的研究为理解病毒致病机制铺平了道路,包括那些与在影响免疫功能低下患者的宿主肿瘤中建立感染和传播有关的机制。从病毒感染到恶性肿瘤进展的过程较为缓慢,通常不足以在仅少数受感染个体中建立发展为癌症的转化细胞。因此,病毒感染通常不是癌症的唯一原因,可能还涉及其他环境和宿主因素。特别是,人类嗜T淋巴细胞病毒I型(HTLV-I)被认为是成人T细胞白血病/淋巴瘤(ATL)等淋巴增殖性疾病的致癌病毒,并干扰免疫反应,导致HTLV-I相关脊髓病/热带痉挛性截瘫(HAM/TSP)。尽管针对该病毒存在强烈的适应性免疫反应,但HTLV-I感染在经过较长潜伏期(15 - 30年)后,仅在一小部分受感染个体(2 - 5%)中导致ATL。总体而言,这些情况为研究哺乳动物细胞中致瘤性的分子基础提供了前景。在本综述中,HTLV-I的致癌性被视为与ATL相关的一种致癌病毒。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ace7/3881257/1c6a3178cad1/ijbms-16-179-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ace7/3881257/2ff08f0d1558/ijbms-16-179-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ace7/3881257/a6a127c6810a/ijbms-16-179-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ace7/3881257/ae03cd836341/ijbms-16-179-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ace7/3881257/1c6a3178cad1/ijbms-16-179-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ace7/3881257/2ff08f0d1558/ijbms-16-179-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ace7/3881257/a6a127c6810a/ijbms-16-179-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ace7/3881257/ae03cd836341/ijbms-16-179-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ace7/3881257/1c6a3178cad1/ijbms-16-179-g004.jpg

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