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首页> 外文期刊>JAIDS: Journal of acquired immune deficiency syndromes >The role of hydroxyurea in enhancing the virologic control achieved through structured treatment interruption in primary HIV infection: final results from a randomized clinical trial (Pulse).
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The role of hydroxyurea in enhancing the virologic control achieved through structured treatment interruption in primary HIV infection: final results from a randomized clinical trial (Pulse).

机译:羟基脲在原发性HIV感染中通过结构化治疗中断实现的增强病毒控制的作用:一项随机临床试验(Pulse)的最终结果。

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BACKGROUND: Structured treatment interruptions (STIs) have been postulated to improve virologic control in primary HIV infection (PHI) by stimulating HIV-specific T-lymphocyte immunity. The addition of hydroxyurea (HU) may reduce viral production from activated CD4 cells. METHODS: Patients with PHI received a standardized antiretroviral (ARV) regimen consisting of indinavir 800 mg twice daily (BID), ritonavir 100 mg BID, didanosine 400 mg (QD), and either stavudine 40 mg BID or lamivudine 150 mg BID, for up to 12 months and were randomized to HU 500 mg BID or not. If viral suppression (<50 copies/mL) was achieved, up to 3 STIs were undertaken. Two ARV cycles were allowed after each interruption if virologic rebound to more than 5000 RNA copies/mL occurred. Treatment success was defined as maintaining viral loads below 5000 copies/mL for 6 months after ARV interruption. RESULTS: Sixty-eight male homosexual patients were randomized: 35 to ARV + HU and 33 to ARV-alone. Median baseline HIV RNA was 5.73 log10 copies/mL, and median CD4 T-lymphocyte count was 517 cells/microL. Treatment success was not significantly different between those receiving and not receiving HU, with 9 (26%) and 9 (27%), respectively, maintaining viral load at less than 5000 copies/mL in each group (P = 0.88). Virologic control was achieved by 11 (19%) of 59 after 1 STI, 1 (2%) of 41 after 2 STIs, and 6 (17%) of 36 after the third STI. Serious adverse events were recorded for 9 (26%) of 35 of patients using HU and 3 (9%) of 33 in the ARV-only group (P = 0.28). CD4 cell increases were significantly blunted for the HU group compared to the ARV-alone group after the initial treatment phase (+101 cells vs. +196 cells, respectively, P = 0.006). CONCLUSIONS: Hydroxyurea was not found to be beneficial when used in association with STIs in patients during PHI.
机译:背景:结构性治疗中断(STIs)已被认为可以通过刺激HIV特异性T淋巴细胞免疫来改善原发性HIV感染(PHI)的病毒学控制。羟基脲(HU)的添加可能会减少活化CD4细胞产生的病毒。方法:PHI患者接受标准化的抗逆转录病毒(ARV)方案,其中包括茚达那韦800 mg每天两次(BID),利托那韦100 mg BID,去羟肌苷400 mg(QD)和司他夫定40 mg BID或拉米夫定150 mg BID到12个月,并随机分配给HU 500 mg BID。如果达到病毒抑制(<50拷贝/ mL),则最多进行3次STI。如果发生病毒反弹至5000 RNA拷贝/ mL以上,则每次中断后允许两个ARV周期。治疗成功的定义是在ARV中断后6个月内保持病毒载量低于5000拷贝/ mL。结果:68例男性同性恋患者被随机分组​​:35例接受ARV + HU治疗,33例单独接受ARV治疗。基线HIV RNA的中位数为5.73 log10拷贝/毫升,CD4 T淋巴细胞的中位数为517细胞/微升。接受和不接受HU治疗者之间的治疗成功率无显着差异,分别为9(26%)和9(27%),每组的病毒载量保持在5000拷贝/ mL以下(P = 0.88)。进行一次性传播感染后,进行病毒学控制的比例为11(19%),占59%;两次发生性传播感染后,占41(1)(2%)的比例为36;第三次发生性传播感染后,其比例为36(6)(17%)。在仅使用抗逆转录病毒治疗的组中,有35名使用HU的患者中有9名(26%)发生严重不良事件,仅ARV组的33名中有3名(9%)发生了严重事件(P = 0.28)。与单独治疗后的ARV组相比,HU组的CD4细胞增加明显减弱(分别为+101细胞对+196细胞,P = 0.006)。结论:在PHI期间,与STIs联合使用时,羟基脲未发现有益。

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