Biotron Limited, North Ryde, Australia.
HIV-Netherlands Australia Thailand Research Collaboration, Thai Red Cross AIDS Research Centre, Bangkok, Thailand.
J Infect Dis. 2021 Jun 4;223(11):1914-1922. doi: 10.1093/infdis/jiaa635.
BIT225 is a first-in-class inhibitor of human immunodeficiency virus (HIV) type 1 Vpu. A phase II trial enrolled 36 HIV-1-infected, treatment-naive participants in Thailand to receive standard-of-care antiretroviral therapy (ART), tenofovir disoproxil fumarate/emtricitabine/efavirenz (Atripla), with 100 or 200 mg of BIT225 or placebo (daily) for 12 weeks. Combined treatment with BIT225 and ART was found to be generally safe and well tolerated, with antiviral efficacy comparable to that of ART alone. The secondary end point-soluble CD163, a marker of monocyte/macrophage inflammation-was noted to be significantly decreased in the BIT225 arm. Plasma-derived activated CD4+ and CD8+ T cells, natural killer cells, and interleukin 21 were increased in those treated with BIT225. These findings are consistent with inhibition of the known effects of HIV Vpu and may reflect clinically important modulation of inflammatory and immune function. Further clinical study is planned to both confirm and extend these important findings in treatment-naive, and treatment-experienced individuals. Clinical Trials Registration. Australian New Zealand Clinical Trials Registry (Universal Trial Number U1111-1191-2194).
BIT225 是一种新型人免疫缺陷病毒 (HIV) 1 型 Vpu 的抑制剂。一项 II 期临床试验在泰国招募了 36 名 HIV-1 感染、未经治疗的参与者,他们接受了标准的抗逆转录病毒治疗 (ART),即富马酸替诺福韦二吡呋酯/恩曲他滨/依法韦仑 (Atripla),同时每日接受 100 或 200mg 的 BIT225 或安慰剂治疗 12 周。结果发现,与 ART 单独治疗相比,联合使用 BIT225 和 ART 通常是安全且耐受良好的,并且具有相似的抗病毒疗效。次要终点可溶性 CD163(单核细胞/巨噬细胞炎症的标志物)在 BIT225 组中显著降低。接受 BIT225 治疗的患者血浆中激活的 CD4+和 CD8+T 细胞、自然杀伤细胞和白细胞介素 21 增加。这些发现与 HIV Vpu 的已知作用抑制一致,可能反映了对炎症和免疫功能的重要临床调节。计划进一步进行临床研究,以在未经治疗和治疗经验丰富的个体中确认和扩展这些重要发现。临床试验注册。澳大利亚新西兰临床试验注册处(通用试验编号 U1111-1191-2194)。