Jain Anshika, Canepa Gaspar E, Liou Mei-Ling, Fledderman Emily L, Chapoval Andrei I, Xiao Lingzhi, Mukherjee Ipsita, Balogun Bushirat M, Huaman-Vergara Hellen, Galvin Jeffrey A, Kumar Princy N, Bordon José, Conant Marcus A, Boyle Jefferey S
American Gene Technologies International, Inc., Rockville, MD, United States.
Division of Infectious Diseases and Tropical Medicine, Georgetown University School of Medicine, Washington, DC, United States.
Front Med (Lausanne). 2024 May 14;11:1342476. doi: 10.3389/fmed.2024.1342476. eCollection 2024.
Human Immunodeficiency Virus (HIV) remains a global health challenge, and novel approaches to improve HIV control are significantly important. The cell and gene therapy product AGT103-T was previously evaluated (NCT04561258) for safety, immunogenicity, and persistence in seven patients for up to 180 days post infusion. In this study, we sought to investigate the impact of AGT103-T treatment upon analytical treatment interruptions (ATIs). Six patients previously infused with AGT103-T were enrolled into an ATI study (NCT05540964), wherein they suspended their antiretroviral therapy (ART) until their viral load reached 100,000 copies/mL in two successive visits, or their CD4 count was reduced to below 300 cells/μL. During the ATI, all patients experienced viral rebound followed by a notable expansion in HIV specific immune responses. The participants demonstrated up to a five-fold increase in total CD8 counts over baseline approximately 1-2 weeks followed by the peak viremia. This coincided with a rise in HIV-specific CD8 T cells, which was attributed to the increase in antigen availability and memory recall. Thus, the protocol was amended to include a second ATI with the first ATI serving as an "auto-vaccination." Four patients participated in a second ATI. During the second ATI, the Gag-specific CD8 T cells were either maintained or rose in response to viral rebound and the peak viremia was substantially decreased. The patients reached a viral set point ranging from 7,000 copies/mL to 25,000 copies/mL. Upon resuming ART, all participants achieved viral control more rapidly than during the first ATI, with CD4 counts remaining within 10% of baseline measurements and without any serious adverse events or evidence of drug resistance. In summary, the rise in CD8 counts and the viral suppression observed in 100% of the study participants are novel observations demonstrating that AGT103-T gene therapy when combined with multiple ATIs, is a safe and effective approach for achieving viral control, with viral setpoints consistently below 25,000 copies/mL and relatively stable CD4 T cell counts. We conclude that HIV cure-oriented cell and gene therapy trials should include ATI and may benefit from designs that include multiple ATIs when induction of CD8 T cells is required to establish viral control.
人类免疫缺陷病毒(HIV)仍然是一项全球性的健康挑战,因此,采用新方法改善HIV控制具有极其重要的意义。细胞和基因治疗产品AGT103-T先前已针对7名患者进行了安全性、免疫原性及持久性评估(NCT04561258),观察期长达输注后180天。在本研究中,我们试图探究AGT103-T治疗对分析性治疗中断(ATI)的影响。6名先前接受AGT103-T输注的患者被纳入一项ATI研究(NCT05540964),在此研究中,他们暂停抗逆转录病毒疗法(ART),直至连续两次就诊时病毒载量达到100,000拷贝/毫升,或其CD4细胞计数降至300细胞/微升以下。在ATI期间,所有患者均经历了病毒反弹,随后HIV特异性免疫反应显著增强。在病毒血症达到峰值前约1至2周,参与者的总CD8细胞计数相比基线水平最多增加了五倍。这与HIV特异性CD8 T细胞的增加同时出现,这归因于抗原可用性的增加和记忆回忆。因此,研究方案进行了修订,纳入了第二次ATI,第一次ATI作为“自体疫苗接种”。4名患者参与了第二次ATI。在第二次ATI期间,Gag特异性CD8 T细胞要么维持在原有水平,要么因病毒反弹而增加,且病毒血症峰值大幅下降。患者的病毒载量稳定在7,000拷贝/毫升至25,000拷贝/毫升之间。恢复ART后,所有参与者实现病毒控制的速度均比第一次ATI期间更快,CD4细胞计数保持在基线测量值的10%以内,且未出现任何严重不良事件或耐药迹象。总之,在100%的研究参与者中观察到的CD8细胞计数增加和病毒抑制是新的发现,表明AGT103-T基因疗法与多次ATI相结合,是实现病毒控制的一种安全有效的方法,病毒载量稳定点始终低于25,000拷贝/毫升,且CD4 T细胞计数相对稳定。我们得出结论,以治愈HIV为导向的细胞和基因治疗试验应包括ATI,并且在需要诱导CD8 T细胞来建立病毒控制时,可能会从包含多次ATI的设计中受益。