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HIV-1 进入抑制剂肽拟似物的治疗潜力。

Therapeutic potential of HIV-1 entry inhibitor peptidomimetics.

机构信息

Department of Biochemistry, Cell and Molecular Biology, West African Centre for Cell Biology of Infectious Pathogens, College of Basic and Applied Sciences, University of Ghana, Accra 00233, Ghana.

Department of Biomedical Engineering, School of Engineering Sciences, College of Basic and Applied Sciences, University of Ghana, Accra 00233, Ghana.

出版信息

Exp Biol Med (Maywood). 2021 May;246(9):1060-1068. doi: 10.1177/1535370221990870. Epub 2021 Feb 17.

Abstract

Human immunodeficiency virus 1 (HIV-1) infection remains a public health concern globally. Although great strides in the management of HIV-1 have been achieved, current highly active antiretroviral therapy is limited by multidrug resistance, prolonged use-related effects, and inability to purge the HIV-1 latent pool. Even though novel therapeutic options with HIV-1 broadly neutralizing antibodies (bNAbs) are being explored, the scalability of bNAbs is limited by economic cost of production and obligatory requirement for parenteral administration. However, these limitations can be addressed by antibody mimetics/peptidomimetics of HIV-1 bNAbs. In this review we discuss the limitations of HIV-1 bNAbs as HIV-1 entry inhibitors and explore the potential therapeutic use of antibody mimetics/peptidomimetics of HIV-1 entry inhibitors as an alternative for HIV-1 bNAbs. We highlight the reduced cost of production, high specificity, and oral bioavailability of peptidomimetics compared to bNAbs to demonstrate their suitability as candidates for novel HIV-1 therapy and conclude with some perspectives on future research toward HIV-1 novel drug discovery.

摘要

人类免疫缺陷病毒 1(HIV-1)感染仍然是全球公共卫生关注的问题。尽管在 HIV-1 管理方面取得了重大进展,但目前的高效抗逆转录病毒疗法受到多药耐药性、长期使用相关影响以及无法清除 HIV-1 潜伏池的限制。尽管正在探索具有 HIV-1 广泛中和抗体(bNAbs)的新型治疗选择,但 bNAbs 的可扩展性受到生产的经济成本和必需的肠胃外给药的限制。然而,这些限制可以通过 HIV-1 bNAbs 的抗体模拟物/肽模拟物来解决。在这篇综述中,我们讨论了 HIV-1 bNAbs 作为 HIV-1 进入抑制剂的局限性,并探讨了 HIV-1 进入抑制剂的抗体模拟物/肽模拟物作为 HIV-1 bNAbs 的替代物的潜在治疗用途。我们强调了与 bNAbs 相比,肽模拟物在生产、高特异性和口服生物利用度方面的成本降低,以证明它们适合作为新型 HIV-1 治疗的候选物,并对未来针对 HIV-1 新型药物发现的研究提出了一些看法。

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