Small-molecule HIV-1 entry inhibitors targeting the epitopes of broadly neutralizing antibodies

Cell Chem Biol. 2022 May 19;29(5):757-773. doi: 10.1016/j.chembiol.2022.03.009. Epub 2022 Mar 29.

Abstract

Highly active antiretroviral therapy currently used for HIV/AIDS has significantly increased the life expectancy of HIV-infected individuals. It has also improved the quality of life, reduced mortality, and decreased the incidence of AIDS and HIV-related conditions. Currently, however, affected individuals are typically on a lifetime course of several therapeutic drugs, all with the potential for associated toxicity and emergence of resistance. This calls for development of novel, potent, and broad anti-HIV agents able to stop the spread of HIV/AIDS. Significant progress has been made toward identification of anti-HIV-1 broadly neutralizing antibodies (bNAbs). However, antibody-based drugs are costly to produce and store. Administration (by injection only) and other obstacles limit clinical use. In recent years, several highly promising small-molecule HIV-1 entry inhibitors targeting the epitopes of bNAbs have been developed. These newly developed compounds are the focus of the present article.

Keywords: HIV; broadly neutralizing antibodies; entry inhibitors; epitopes; small molecule.

Publication types

  • Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antibodies, Neutralizing / pharmacology
  • Broadly Neutralizing Antibodies
  • Epitopes
  • HIV Antibodies / therapeutic use
  • HIV Infections* / drug therapy
  • HIV-1*
  • Humans
  • Quality of Life
  • env Gene Products, Human Immunodeficiency Virus

Substances

  • Antibodies, Neutralizing
  • Broadly Neutralizing Antibodies
  • Epitopes
  • HIV Antibodies
  • env Gene Products, Human Immunodeficiency Virus