Liner Kevin J, Hall Colin D, Robertson Kevin R
Department of Neurology, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
J Neurovirol. 2007 Aug;13(4):291-304. doi: 10.1080/13550280701422383.
Among the many variables affecting transmission and pathogenesis of the human immunodeficiency virus type 1(HIV-1), the effects of HIV subtypes, or clades, on disease progression remain unclear. Although debated, some studies have found that the variable env and pol sequences of different subtypes of HIV-1 may endow some subtypes with greater degrees of cell tropism, virulence, and drug resistance, which may lead to differences in overall disease progression. HIV-associated dementia (HAD) appears to be associated with viral diversity and markers of immune activation. Africa has the highest prevalence of HIV, largest viral diversity, and is where clade recombination occurs most frequently. All of these factors would suggest that HAD would pose the largest threat in this region of the world. Although investigations into the effects of different subtypes on overall disease progression are well documented, few have looked into the effects of subtypes on neurological disease progression. This review highlights the need for more international research involving the neurological effects and especially the clinical presentation of dementia for the entire range of the group M HIV-1 subtypes.
在影响人类免疫缺陷病毒1型(HIV-1)传播和发病机制的众多变量中,HIV亚型或进化枝对疾病进展的影响仍不明确。尽管存在争议,但一些研究发现,HIV-1不同亚型的可变env和pol序列可能使某些亚型具有更高程度的细胞嗜性、毒力和耐药性,这可能导致总体疾病进展存在差异。HIV相关痴呆(HAD)似乎与病毒多样性和免疫激活标志物有关。非洲是HIV患病率最高、病毒多样性最大且进化枝重组最频繁的地区。所有这些因素都表明,HAD在世界这一地区构成的威胁最大。尽管关于不同亚型对总体疾病进展影响的研究有充分记录,但很少有人研究亚型对神经疾病进展的影响。本综述强调需要开展更多国际研究,涉及M组HIV-1亚型全范围内的神经学影响,尤其是痴呆的临床表现。