Chen Siyan, Xu Qihua, Wang Jian, Tan Xinghua
Artemisia annua Research Center, Guangzhou University of Chinese Medicine, Guangzhou, China.
Chinese Medicine Research Center for AIDS Prevention and Treatment, China Academy of Chinese Medical Sciences, Beijing, China.
AIDS Res Hum Retroviruses. 2022 Feb;38(2):100-110. doi: 10.1089/AID.2020.0254. Epub 2021 Jun 2.
The level of T cell activation is a better predictor of CD4 T cell depletion in highly active antiretroviral therapy (HAART) patients than viral load. Artesunate is an artemisinin derivative that has an immunomodulatory effect. This study investigated whether artesunate tablet reduces T cell activation and improves immune reconstitution among patients with suboptimal immune recovery despite receiving long-term effective HAART. This was a randomized prospective parallel open-label trial consisting of 45 participants whose plasma HIV load was effectively suppressed by HAART for >18 months and who had CD4 T cell counts of <300 cells/μL or an increase of <20% from baseline. The patients were randomized 2:1 into the artesunate group or the control group and received artesunate tablets (orally, 50 mg two times daily) combined with HAART or HAART alone, respectively. T cell subsets, activation markers, clinical symptoms, viral load, and side effects were assessed. By 48 weeks, artesunate tablet did not improve CD4 T cell recovery or reduce the activation of T cell subsets but induced in a smaller decline in the expression of T cell activation markers among HAART patients with incomplete immune responses. However, artesunate tablet did appear to reduce the level of T cell apoptosis. One subject developed moderate anemia. Long-term use of artesunate tablet is unlikely to produce substantial clinical benefits in patients receiving HAART who exhibit an incomplete immune response.
在高效抗逆转录病毒治疗(HAART)患者中,T细胞活化水平比病毒载量更能预测CD4 T细胞耗竭情况。青蒿琥酯是一种具有免疫调节作用的青蒿素衍生物。本研究调查了青蒿琥酯片是否能降低T细胞活化水平,并改善在接受长期有效HAART治疗后免疫恢复仍不理想的患者的免疫重建情况。这是一项随机前瞻性平行开放标签试验,共有45名参与者,其血浆HIV载量被HAART有效抑制超过18个月,且CD4 T细胞计数<300个/μL或较基线增加<20%。患者按2:1随机分为青蒿琥酯组或对照组,分别接受青蒿琥酯片(口服,每日两次,每次50mg)联合HAART或单独接受HAART治疗。评估了T细胞亚群、活化标志物、临床症状、病毒载量和副作用。到48周时,青蒿琥酯片并未改善CD4 T细胞恢复情况或降低T细胞亚群的活化,但在免疫反应不完全的HAART患者中,青蒿琥酯片使T细胞活化标志物的表达下降幅度较小。然而,青蒿琥酯片似乎确实降低了T细胞凋亡水平。有一名受试者出现了中度贫血。对于接受HAART且免疫反应不完全的患者,长期使用青蒿琥酯片不太可能产生显著的临床益处。