Rétrovirus humains HTLV-1 et HTLV-2

A Gessain (Chef d'unité)
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引用次数: 2

Abstract

HTLV-1 (Human T cell leukemia /Lymphoma virus type 1), the first oncogenic retrovirus discovered in Human in 1980, possesses the classical gag, pol, and env genes coding the structural and enzymatic proteins as well as a unique region (named pX) coding the regulatory proteins Tax and Rex. Tax stimulates the viral transcription and also plays a fundamental role in leukemogenesis by modifying the expression of several genes crucial for the survival as well as the proliferation of the cell. HTLV-1 is principally an etiological agent of two diseases associated to a very bad prognosis: malignant T cell lymphoproliferation; the adult T cell leukemia/lymphoma (ATLL) and a chronic neuromyelopathy, the tropical spastic parapareris/HTLV-1 associated myelopathy. HTLV-1 is not ubiquitous. Fifteen to 20 millions of individuals are infected worldwide, mainly in high endemic areas such as Southern Japan, intertropical Africa, the Caribbean region and the surrounding areas including parts of South America. In these areas, 0.5 % to 50 % of the people, depending on age and sex, are infected by the virus and are therefore HTLV-1 seropositive. HTLV-1 is transmitted from mother to child through prolonged breast-feeding, by sexual contacts mainly from male to female and by blood transfusion through passage of infected lymphocytes. The distribution of the different molecular subtypes (genotypes) is linked to the geographical origin of the infected populations rather than to the pathology (leukemia vs. neuromyelopathy). The great genetic stability of HTLV-1 can be used as a molecular mean to gain new insights into the origin, evolution and dissemination of this virus and of its host. HTLV-2, which is genetically related to HTLV-1, differs however from the latter by some specific epidemiological features. Indeed, HTLV-2 is mainly endemic in several Amerindians tribes and in some groups of intravenous drug users living mainly in the United States and in some European countries. Few cases of chronic neuromyelopathy have been associated with HTLV-2 and there is still no strong evidence that this retrovirus is linked to any malignant lymphoproliferation.

人逆转录病毒HTLV-1和HTLV-2
HTLV-1(人T细胞白血病/淋巴瘤病毒1型)是1980年在人类中发现的第一种致癌逆转录病毒,具有编码结构蛋白和酶蛋白的经典gag、pol和env基因,以及编码调节蛋白Tax和Rex的独特区域(命名为pX)。Tax刺激病毒转录,并通过改变对细胞生存和增殖至关重要的几个基因的表达,在白血病发生中发挥重要作用。HTLV-1主要是与非常糟糕的预后相关的两种疾病的病原体:恶性T细胞淋巴增殖;成人T细胞白血病/淋巴瘤(ATLL)和慢性神经脊髓病、热带痉挛性伴轻瘫/HTLV-1相关脊髓病。HTLV-1并非无处不在。全世界有1500万至2000万人感染,主要发生在高流行地区,如日本南部、热带非洲、加勒比地区和包括南美洲部分地区在内的周边地区。在这些地区,根据年龄和性别,0.5%至50%的人感染了该病毒,因此HTLV-1血清呈阳性。HTLV-1通过长期母乳喂养、主要从男性到女性的性接触以及通过受感染淋巴细胞的输血从母亲传播给儿童。不同分子亚型(基因型)的分布与感染人群的地理来源有关,而不是与病理学(白血病与神经脊髓病)有关。HTLV-1的巨大遗传稳定性可以作为一种分子手段,以获得对该病毒及其宿主的起源、进化和传播的新见解。HTLV-2与HTLV-1在基因上有亲缘关系,但与后者的不同之处在于一些特定的流行病学特征。事实上,HTLV-2主要在几个美洲印第安人部落和主要生活在美国和一些欧洲国家的一些静脉注射吸毒者群体中流行。很少有慢性神经脊髓病病例与HTLV-2有关,目前还没有强有力的证据表明这种逆转录病毒与任何恶性淋巴增殖有关。
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