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当前肽和蛋白质候选药物在疫苗时代后挑战 HIV 治疗。

Current Peptide and Protein Candidates Challenging HIV Therapy beyond the Vaccine Era.

机构信息

Division of Clinical Immunology, Department of Medical Technology, Faculty of Associated Medical Sciences, Chiang Mai University, Chiang Mai 50200, Thailand.

Center of Biomolecular Therapy and Diagnostic, Faculty of Associated Medical Sciences, Chiang Mai University, Chiang Mai 50200, Thailand.

出版信息

Viruses. 2017 Sep 29;9(10):281. doi: 10.3390/v9100281.

Abstract

Human immunodeficiency virus (HIV) is a causative agent of acquired immune deficiency syndrome (AIDS). Highly active antiretroviral therapy (HAART) can slow down the replication of HIV-1, leading to an improvement in the survival of HIV-1-infected patients. However, drug toxicities and poor drug administration has led to the emergence of a drug-resistant strain. HIV-1 immunotherapy has been continuously developed, but antibody therapy and HIV vaccines take time to improve its efficiency and have limitations. HIV-1-specific chimeric antigen receptor (CAR)-based immunotherapy founded on neutralizing antibodies is now being developed. In HIV-1 therapy, anti-HIV chimeric antigen receptors showed promising data in the suppression of HIV-1 replication; however, autologous transfusion is still a problem. This has led to the development of effective peptides and proteins for an alternative HIV-1 treatment. In this paper, we provide a comprehensive review of potent anti-HIV-1 peptides and proteins that reveal promising therapeutic activities. The inhibitory mechanisms of each therapeutic molecule in the different stages of the HIV-1 life cycle will be discussed herein.

摘要

人类免疫缺陷病毒(HIV)是获得性免疫缺陷综合征(AIDS)的病原体。高效抗逆转录病毒疗法(HAART)可以减缓 HIV-1 的复制,从而改善 HIV-1 感染患者的生存。然而,药物毒性和给药不当导致了耐药株的出现。HIV-1 免疫疗法一直在不断发展,但抗体疗法和 HIV 疫苗需要时间来提高其效率并存在局限性。现在正在开发基于中和抗体的 HIV-1 特异性嵌合抗原受体(CAR)免疫疗法。在 HIV-1 治疗中,抗 HIV 嵌合抗原受体在抑制 HIV-1 复制方面显示出有希望的数据;然而,自体输血仍然是一个问题。这导致了用于替代 HIV-1 治疗的有效肽和蛋白质的发展。在本文中,我们提供了对强效抗 HIV-1 肽和蛋白质的全面综述,这些肽和蛋白质显示出有希望的治疗活性。本文将讨论每个治疗分子在 HIV-1 生命周期的不同阶段中的抑制机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b65/5691633/dc6303667865/viruses-09-00281-g001.jpg

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