Therapeutic potential of HIV-1 entry inhibitor peptidomimetics

被引:2
|
作者
Korie, Nneka P. U. [1 ]
Tandoh, Kwesi Z. [1 ]
Kwofie, Samuel K. [1 ,2 ]
Quaye, Osbourne [1 ]
机构
[1] Univ Ghana, Coll Basic & Appl Sci, West African Ctr Cell Biol Infect Pathogens, Dept Biochem Cell & Mol Biol, Accra 00233, Ghana
[2] Univ Ghana, Coll Basic & Appl Sci, Sch Engn Sci, Dept Biomed Engn, Accra 00233, Ghana
关键词
Human immunodeficiency virus 1; broadly neutralizing antibodies; peptidomimetics; entry inhibitors; antiretroviral therapy; HIV-1 novel drug discovery; BROADLY NEUTRALIZING ANTIBODIES; HUMAN-IMMUNODEFICIENCY-VIRUS; PEPTIDE TRIAZOLE INACTIVATORS; MONOCLONAL-ANTIBODY; PROTEASE INHIBITORS; CD4; RECEPTOR; BINDING-SITE; ENVELOPE; MOLECULE; DESIGN;
D O I
10.1177/1535370221990870
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
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.
引用
收藏
页码:1060 / 1068
页数:9
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