Bourboulia Dimitra, Aldam Diana, Lagos Dimitrios, Allen Elizabeth, Williams Ian, Cornforth David, Copas Andrew, Boshoff Chris
Wolfson Institute for Biomedical Research and the Department of Sexually Transmitted Diseases, University College London, London, UK.
AIDS. 2004 Feb 20;18(3):485-93. doi: 10.1097/00002030-200402200-00015.
To investigate the effect of highly active antiretroviral therapy (HAART) on Kaposi sarcoma-associated herpesvirus (KSHV) DNA load, anti-KSHV antibody responses and KSHV-specific CD8 T cell responses in HIV-infected individuals over a 2 year period.
Prospective study of 27 HIV-infected antiretroviral therapy-naive individuals, with (n = 4) and without KS (n = 23), before HAART and at 3-month intervals, during treatment with HAART.
Sequential blood samples were collected for anti-KSHV antibody detection, KSHV DNA load in peripheral blood mononuclear cells (PBMC) and plasma, HIV Gag-specific and KSHV-specific CD8 T cell responses, HIV-1 plasma RNA load and CD4 and CD8 T cell counts.
KSHV DNA in PBMC and plasma became less detectable over time during HAART, in particular after 12 months. KSHV DNA was undetectable in plasma after 24 months on HAART. Anti-KSHV lytic, but not latent, antibody levels increased within 12 months of treatment. KSHV-specific CD8 T cell responses were absent prior to HAART but became detectable in some patients within 6 months of starting treatment, and continued to increase thereafter.
HAART (both protease inhibitor-based and non-nucleoside reverse transcriptase inhibitor-based antiretroviral combinations) is associated with immune reconstitution to KSHV and with undetectable KSHV viraemia. However, this restoration is apparent (in particular) only after a relatively long (> 24 months) period of treatment. These immune responses could contribute to the decreased incidence of KS during HAART, but it is unlikely to be a complete explanation for the often rapid resolution of KS when HAART is started.
研究高效抗逆转录病毒疗法(HAART)在2年期间对HIV感染个体中卡波西肉瘤相关疱疹病毒(KSHV)DNA载量、抗KSHV抗体反应和KSHV特异性CD8 T细胞反应的影响。
对27例未接受过抗逆转录病毒治疗的HIV感染个体进行前瞻性研究,其中4例患有卡波西肉瘤(KS),23例未患KS,在HAART治疗前以及HAART治疗期间每隔3个月进行观察。
采集系列血样,用于检测抗KSHV抗体、外周血单个核细胞(PBMC)和血浆中的KSHV DNA载量、HIV Gag特异性和KSHV特异性CD8 T细胞反应、HIV-1血浆RNA载量以及CD4和CD8 T细胞计数。
在HAART治疗期间,随着时间推移,PBMC和血浆中的KSHV DNA越来越难以检测到,尤其是在12个月后。接受HAART治疗24个月后,血浆中未检测到KSHV DNA。治疗12个月内,抗KSHV裂解抗体水平升高,但潜伏抗体水平未升高。在HAART治疗前未检测到KSHV特异性CD8 T细胞反应,但在一些患者开始治疗后6个月内可检测到,此后持续增加。
HAART(基于蛋白酶抑制剂和基于非核苷类逆转录酶抑制剂的抗逆转录病毒联合疗法)与针对KSHV的免疫重建以及无法检测到的KSHV病毒血症有关。然而,这种恢复(尤其)仅在相对较长(>24个月)的治疗期后才明显。这些免疫反应可能有助于降低HAART治疗期间KS的发病率,但不太可能完全解释开始HAART治疗时KS通常迅速消退的原因。