Elovaara I, Seppälä I, Poutiainen E, Suni J, Valle S L
Department of Neurology, University of Helsinki, Finland.
Neurology. 1988 Sep;38(9):1451-6. doi: 10.1212/wnl.38.9.1451.
We analyzed the intrathecal humoral immunologic response in 42 human immunodeficiency virus (HIV)-infected patients. Eighteen patients had clinical neurologic abnormalities, while the remaining 24 patients were neurologically symptom-free. Nine of the neurologically symptomatic patients at early infection had slight neurologic dysfunction; in nine other subjects at late infection, the neurologic impairment was moderate or severe. When compared with symptom-free patients, neurologically symptomatic patients had increased intra-blood-brain barrier (BBB) HIV-specific IgG (p less than 0.001) and total IgG synthesis (p less than 0.01) with oligoclonal bands (OCBs) in the CSF and/or serum (11/18 versus 3/24). At early stages of the infection, neurologically symptomatic patients showed increased total intrathecal IgG synthesis (9/9) coincident with OCBs in the CSF and serum (7/9) and slight mononuclear pleocytosis (7/9), but less frequent HIV-specific IgG production within the CNS (6/9). In advanced infection, the number of neurologically symptomatic patients with intrathecal HIV-specific IgG synthesis (8/9) was higher, while the number of those with increased total intra-BBB IgG synthesis (5/9; p less than 0.01), OCBs (4/9), and increased CSF leukocyte count (1/9; p less than 0.001) was lower than at early infection. Our data suggest humoral intra-BBB immunoactivation at early stages of HIV infection followed by declining B cell response within the CNS at advanced infection.
我们分析了42例人类免疫缺陷病毒(HIV)感染患者的鞘内体液免疫反应。18例患者有临床神经学异常,其余24例患者无神经学症状。18例早期感染且有神经学症状的患者中有9例有轻微神经功能障碍;9例晚期感染的其他患者神经损伤为中度或重度。与无症状患者相比,有神经学症状的患者血脑屏障(BBB)内HIV特异性IgG增加(p<0.001),总IgG合成增加(p<0.01),脑脊液和/或血清中有寡克隆带(OCB)(11/18比3/24)。在感染早期,有神经学症状的患者鞘内总IgG合成增加(9/9),同时脑脊液和血清中有OCB(7/9)以及轻微单核细胞增多(7/9),但中枢神经系统内HIV特异性IgG产生频率较低(6/9)。在晚期感染中,鞘内有HIV特异性IgG合成的有神经学症状的患者数量较多(8/9),而血脑屏障内总IgG合成增加(5/9;p<0.01)、有OCB(4/9)以及脑脊液白细胞计数增加(1/9;p<0.001)的患者数量低于早期感染。我们的数据表明,HIV感染早期血脑屏障内体液免疫激活,随后晚期感染时中枢神经系统内B细胞反应下降。