Kelder W, McArthur J C, Nance-Sproson T, McClernon D, Griffin D E
Department of Molecular Microbiology and Immunology, Johns Hopkins University School of Hygiene and Public Health, Baltimore, MD 21205, USA.
Ann Neurol. 1998 Nov;44(5):831-5. doi: 10.1002/ana.410440521.
Human immunodeficiency virus-associated dementia (HAD) is associated with increased numbers of activated central nervous system (CNS) macrophages. Chemokines, which regulate infiltration of macrophages, were measured in the cerebrospinal fluid (CSF) of human immunodeficiency virus (HIV)-negative and HIV-positive individuals with and without neurological disease. Monocyte chemotactic protein (MCP)-1 and RANTES (but not MCP-3), macrophage inflammatory protein (MIP)-1alpha, MIP-1beta, or interleukin-8 (IL-8) was higher in HAD. MCP-1 correlated with CSF viral load and severity of dementia, and it increased over time in patients who developed dementia.
人类免疫缺陷病毒相关痴呆(HAD)与中枢神经系统(CNS)中活化巨噬细胞数量增加有关。在患有和未患有神经疾病的人类免疫缺陷病毒(HIV)阴性及HIV阳性个体的脑脊液(CSF)中,对调节巨噬细胞浸润的趋化因子进行了检测。单核细胞趋化蛋白(MCP)-1和调节激活正常T细胞表达和分泌的趋化因子(RANTES)(而非MCP-3)、巨噬细胞炎性蛋白(MIP)-1α、MIP-1β或白细胞介素-8(IL-8)在HAD患者中含量更高。MCP-1与脑脊液病毒载量及痴呆严重程度相关,并且在发生痴呆的患者中随时间增加。