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在接受抗CD4结构域1抗体和来那卡韦治疗的个体中,多重耐药HIV的病毒学持续抑制

Sustained virologic suppression of multidrug-resistant HIV in an individual treated with anti-CD4 domain 1 antibody and lenacapavir.

作者信息

Rai M Ali, Blazkova Jana, Kardava Lela, Justement Jesse S, Shi Victoria, Manning Maegan R, Shahid Aniqa, Dong Winnie, Kennedy Brooke D, Sewack Adeline B, Higgins Jeanette, Buckner Clarisa M, Gittens Kathleen, West Raymond E, Devanathan Aaron S, Mangusan Ralph, Lurain Kathryn, Ramaswami Ramya, Yarchoan Robert, Sneller Michael C, Pau Alice K, Brumme Zabrina L, Moir Susan, Chun Tae-Wook

机构信息

Laboratory of Immunoregulation, National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH), Bethesda, MD, USA.

Faculty of Health Sciences, Simon Fraser University, Burnaby, British Columbia, Canada.

出版信息

Nat Med. 2025 Feb;31(2):427-432. doi: 10.1038/s41591-024-03357-0. Epub 2025 Jan 3.

Abstract

The clinical management of people with multidrug-resistant (MDR) human immunodeficiency virus (HIV) remains challenging despite continued development of antiretroviral agents. A 58-year-old male individual with MDR HIV and Kaposi sarcoma (KS) was treated with a new antiretroviral regimen consisting of anti-CD4 domain 1 antibody UB-421 and capsid inhibitor lenacapavir. The individual experienced delayed but sustained suppression of plasma viremia and a substantial increase in the CD4 T cell count. A longitudinal examination of plasma HIV and infectious isolates showed no evidence of viral evolution or the emergence of UB-421- or lenacapavir-resistant viruses. The individual received three cycles of liposomal doxorubicin and five doses of anti-programmed cell death protein 1 (PD-1) monoclonal antibody pembrolizumab that resulted in improvement in KS with flattening of lesions. Our data demonstrate that combination therapy with UB-421 could provide sustained virologic suppression in people harboring MDR HIV with limited therapeutic alternatives.

摘要

尽管抗逆转录病毒药物不断发展,但耐多药(MDR)人类免疫缺陷病毒(HIV)感染者的临床管理仍然具有挑战性。一名58岁的男性耐多药HIV感染者合并卡波西肉瘤(KS),接受了一种新的抗逆转录病毒治疗方案,该方案由抗CD4结构域1抗体UB-421和衣壳抑制剂来那卡帕韦组成。该个体经历了血浆病毒血症延迟但持续的抑制,以及CD4 T细胞计数的大幅增加。对血浆HIV和感染性分离株的纵向检查未发现病毒进化或出现对UB-421或来那卡帕韦耐药病毒的证据。该个体接受了三个周期的脂质体阿霉素和五剂抗程序性细胞死亡蛋白1(PD-1)单克隆抗体帕博利珠单抗治疗,使KS得到改善,病变变平。我们的数据表明,对于治疗选择有限的耐多药HIV感染者,UB-421联合治疗可提供持续的病毒学抑制。

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