Department of Pediatrics, Emory University School of Medicine, Atlanta, GA, USA.
Emory National Primate Research Center, Emory University, Atlanta, GA, USA.
Curr HIV/AIDS Rep. 2024 Feb;21(1):11-29. doi: 10.1007/s11904-023-00686-6. Epub 2024 Jan 16.
An HIV cure that eliminates the viral reservoir or provides viral control without antiretroviral therapy (ART) is an urgent need in children as they face unique challenges, including lifelong ART adherence and the deleterious effects of chronic immune activation. This review highlights the importance of nonhuman primate (NHP) models in developing an HIV cure for children as these models recapitulate the viral pathogenesis and persistence.
Several cure approaches have been explored in infant NHPs, although knowledge gaps remain. Broadly neutralizing antibodies (bNAbs) show promise for controlling viremia and delaying viral rebound after ART interruption but face administration challenges. Adeno-associated virus (AAV) vectors hold the potential for sustained bNAb expression. Therapeutic vaccination induces immune responses against simian retroviruses but has yet to impact the viral reservoir. Combining immunotherapies with latency reversal agents (LRAs) that enhance viral antigen expression should be explored. Current and future cure approaches will require adaptation for the pediatric immune system and unique features of virus persistence, for which NHP models are fundamental to assess their efficacy.
对于儿童来说,消除病毒储存库或在不进行抗逆转录病毒治疗 (ART) 的情况下提供病毒控制是当务之急,因为他们面临着独特的挑战,包括终生的 ART 依从性和慢性免疫激活的有害影响。本综述强调了非人类灵长类动物 (NHP) 模型在开发儿童 HIV 治愈方法方面的重要性,因为这些模型再现了病毒发病机制和持续存在。
已经在婴儿 NHP 中探索了几种治愈方法,但仍存在知识空白。广泛中和抗体 (bNAb) 显示出控制病毒血症和延迟 ART 中断后病毒反弹的潜力,但面临给药挑战。腺相关病毒 (AAV) 载体具有持续表达 bNAb 的潜力。治疗性疫苗可诱导针对猴逆转录病毒的免疫反应,但尚未影响病毒储存库。应探索将免疫疗法与增强病毒抗原表达的潜伏逆转剂 (LRA) 相结合。目前和未来的治愈方法将需要适应儿童免疫系统和病毒持续存在的独特特征,而 NHP 模型对于评估其疗效至关重要。