Kulliyyah of Medicine and Health Sciences (KMHS), Kolej Universiti INSANIAH, 09300 Kuala Ketil, Kedah, Malaysia.
Sunway Institute for Healthcare Development (SIHD), School of Healthcare and Medical Sciences (SHMS), Sunway University, Jalan Universiti, Bandar Sunway, 47500 Subang Jaya, Selangor Darul Ehsan, Malaysia.
Molecules. 2018 Feb 6;23(2):335. doi: 10.3390/molecules23020335.
The discovery of highly active antiretroviral therapy (HAART) in 1996 has significantly reduced the global mortality and morbidity caused by the acquired immunodeficiency syndrome (AIDS). However, the therapeutic strategy of HAART that targets multiple viral proteins may render off-target toxicity and more importantly results in drug-resistant escape mutants. These have been the main challenges for HAART and refinement of this therapeutic strategy is urgently needed. Antibody-mediated treatments are emerging therapeutic modalities for various diseases. Most therapeutic antibodies have been approved by Food and Drug Administration (FDA) mainly for targeting cancers. Previous studies have also demonstrated the promising effect of therapeutic antibodies against HIV-1, but there are several limitations in this therapy, particularly when the viral targets are intracellular proteins. The conventional antibodies do not cross the cell membrane, hence, the pathogenic intracellular proteins cannot be targeted with this classical therapeutic approach. Over the years, the advancement of antibody engineering has permitted the therapeutic antibodies to comprehensively target both extra- and intra-cellular proteins in various infections and diseases. This review aims to update on the current progress in the development of antibody-based treatment against intracellular targets in HIV-1 infection. We also attempt to highlight the challenges and limitations in the development of antibody-based therapeutic modalities against HIV-1.
1996 年发现的高效抗逆转录病毒疗法(HAART)显著降低了获得性免疫缺陷综合征(AIDS)导致的全球死亡率和发病率。然而,HAART 针对多种病毒蛋白的治疗策略可能会产生脱靶毒性,更重要的是会导致耐药逃逸突变体。这些一直是 HAART 的主要挑战,迫切需要对这种治疗策略进行改进。抗体介导的治疗方法是治疗各种疾病的新兴治疗模式。大多数治疗性抗体已被美国食品和药物管理局(FDA)批准,主要用于靶向癌症。先前的研究还表明,治疗性抗体对 HIV-1 有很好的疗效,但这种疗法有几个局限性,特别是当病毒靶标是细胞内蛋白时。传统的抗体不能穿过细胞膜,因此,这种经典的治疗方法不能针对致病的细胞内蛋白。多年来,抗体工程的进步使得治疗性抗体能够全面针对各种感染和疾病的细胞内外蛋白。本综述旨在介绍 HIV-1 感染中针对细胞内靶点的基于抗体的治疗方法的最新进展。我们还试图强调针对 HIV-1 开发基于抗体的治疗模式的挑战和局限性。