THE NEUROPATHOGENESIS OF HIV-1 INFECTION

被引:225
作者
GENDELMAN, HE
LIPTON, SA
TARDIEU, M
BUKRINSKY, MI
NOTTET, HSLM
机构
[1] UNIV NEBRASKA, MED CTR, DEPT MED, OMAHA, NE 68105 USA
[2] UNIV NEBRASKA, MED CTR, EPPLEY INST RES CANC & ALLIED DIS, OMAHA, NE 68182 USA
[3] HARVARD UNIV, SCH MED, BOSTON, MA 02115 USA
[4] CHILDRENS HOSP, MOLEC & CELLULAR NEUROSCI LAB, BOSTON, MA 02115 USA
[5] UNIV PARIS 11, HOP BICETRE, ANRS, LE KREMLIN BICETRE, FRANCE
[6] PICOWER INST, MANHASSET, NY USA
关键词
HIV-1; BRAIN MACROPHAGES; MICROGLIA; CYTOKINES; EICOSANOIDS;
D O I
10.1002/jlb.56.3.389
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
HIV infection in brain revolves around productive viral replication in cells of mononuclear phagocyte lineage, including brain macrophages, microglia, and multinucleated giant cells [1-4]. Together, they are the instigators for cellular and viral neurotoxic activities [5-10]. Several published reports show that viral and/or cellular products produced from HIV-1-infected macrophages injure neurons and induce glial proliferation during advancing central nervous system (CNS) infection [11-18]. These findings are supported by the apparent discrepancy between the distribution and numbers of virus-infected cells and concomitant brain tissue pathology [5, 19]. Whether these soluble factors are indirectly responsible for neuronal damage remains undefined. The identification and regulation of neurotoxins produced from HIV-infected macrophages are central to uncovering how HIV mediates CNS disease. The authors who contributed to this work represent laboratories with overlapping areas of expertise. Broad-based complementary hypotheses regarding HIV neuropathogenesis provided.
引用
收藏
页码:389 / 398
页数:10
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