Adequately Treated Remote Syphilis
Does Not Augment
CNS HIV-1 Expression.

J McArthur, L A White, J McArthur
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Abstract

Objective: The co-occurence of human immunodeficiency virus (HIV) infection and syphilis may accelerate the course of both infections. We investigated whether remote syphilis infection augmented the activation of central nervous system (CNS) HIV infection and increased the frequency of cerebrospinal fluid (CSF) abnormalities.

Methods: The subjects consist of HIV seropositive men who had CSF as part of prospective neurological studies performed at the Johns Hopkins University. Prior syphilis infection was determined by measuring serum FTA-ABS. All subjects had received adequate treatment for syphilis with negative RPR's or RPR's ≤ 1:8 and completed a full neurological examination and underwent lumbar punctures for analysis of cerebrospinal fluid. A range of CSF tests were performed including HIV culture, p24 antigen, β2 microglobulin (β2M) and CSF/albumin ratios.

Results: The FTA positive group was significantly older (p = .005), more advanced in HIV clinical staging (p = .04), had more minor neurological symptoms (p = .03), and was more likely to be on antiretroviral therapy (p = .03). No differences between FTA positive and FTA negative groups were observed either in the frequency of CFS anbormalities or the mean CSF values.

Conclusions: Based on these findings, it appears that adequately treated remote syphilis does not augment HIV-1 expression within the CNS.

适当治疗的远端梅毒不会增强中枢神经系统HIV-1表达。
目的:人类免疫缺陷病毒(HIV)感染与梅毒的同时发生可能加速两者的感染进程。我们研究了远程梅毒感染是否增加了中枢神经系统(CNS) HIV感染的激活,并增加了脑脊液(CSF)异常的频率。方法:受试者包括HIV血清阳性的男性,作为约翰霍普金斯大学前瞻性神经学研究的一部分。通过测定血清FTA-ABS测定既往梅毒感染情况。所有受试者均接受过适当的RPR阴性或RPR阴性梅毒治疗;1:8完成了全面的神经学检查并进行了腰椎穿刺以分析脑脊液。进行一系列脑脊液检测,包括HIV培养、p24抗原、β 2微球蛋白(β 2M)和脑脊液/白蛋白比值。结果:FTA阳性组患者年龄明显增加(p = 0.005), HIV临床分期明显加重(p = 0.04),出现轻微神经症状较多(p = 0.03),接受抗逆转录病毒治疗的可能性较大(p = 0.03)。FTA阳性组和FTA阴性组在CFS异常频率和CSF平均值方面均无差异。结论:基于这些发现,充分治疗的远端梅毒似乎不会增加中枢神经系统内HIV-1的表达。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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