Design Concepts of Virus-Like Particle-Based HIV-1 Vaccines

Front Immunol. 2020 Sep 30:11:573157. doi: 10.3389/fimmu.2020.573157. eCollection 2020.

Abstract

Prophylactic vaccines remain the best approach for controlling the human immunodeficiency virus-1 (HIV-1) transmission. Despite the limited efficacy of the RV144 trial in Thailand, there is still no vaccine candidate that has been proven successful. Consequently, great efforts have been made to improve HIV-1 antigens design and discover delivery platforms for optimal immune elicitation. Owing to immunogenic, structural, and functional diversity, virus-like particles (VLPs) could act as efficient vaccine carriers to display HIV-1 immunogens and provide a variety of HIV-1 vaccine development strategies as well as prime-boost regimes. Here, we describe VLP-based HIV-1 vaccine candidates that have been enrolled in HIV-1 clinical trials and summarize current advances and challenges according to preclinical results obtained from five distinct strategies. This mini-review provides multiple perspectives to help in developing new generations of VLP-based HIV-1 vaccine candidates with better capacity to elicit specific anti-HIV immune responses.

Keywords: HIV-1; broadly neutralizing antibodies; cytotoxic T- lymphocyte response; vaccine; virus-like particles.

Publication types

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

MeSH terms

  • AIDS Vaccines / pharmacology*
  • Animals
  • Drug Design*
  • HIV Antibodies / blood
  • HIV Antigens / immunology
  • HIV Antigens / pharmacology*
  • HIV Infections / immunology
  • HIV Infections / prevention & control*
  • HIV Infections / virology
  • HIV-1 / immunology*
  • Humans
  • Immunogenicity, Vaccine
  • Vaccines, Virus-Like Particle / immunology
  • Vaccines, Virus-Like Particle / pharmacology*

Substances

  • AIDS Vaccines
  • HIV Antibodies
  • HIV Antigens
  • Vaccines, Virus-Like Particle