Development of CAR-T cells for long-term eradication and surveillance of HIV-1 reservoir

Curr Opin Virol. 2019 Oct:38:21-30. doi: 10.1016/j.coviro.2019.04.004. Epub 2019 May 25.

Abstract

Human immunodeficiency virus type 1 (HIV-1) reservoir is a pool of latently infected cells harboring replication-competent proviral DNA that limits antiretroviral therapy. Suppression of HIV-1 by combination antiretroviral therapy (cART) delays progression of the disease but does not eliminate the viral reservoir, necessitating lifetime daily administration of antiretroviral drugs. To achieve durable suppression of viremia without daily therapy, various strategies have been developed, including long-acting antiretroviral drugs (LA-ARVs), broadly neutralizing antibodies (bNAbs), and chimeric antigen receptor T (CAR-T) cells. Here, we summarize and discuss recent breakthroughs in CAR-T cell therapies toward the eradication of HIV-1 reservoir. Although substantial challenges exist, CAR-T cell technology may serve as a promising strategy toward HIV-1 functional cure.

Publication types

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

MeSH terms

  • CD4-Positive T-Lymphocytes / immunology
  • CD4-Positive T-Lymphocytes / metabolism
  • CD4-Positive T-Lymphocytes / virology
  • Disease Reservoirs
  • HIV Antigens / chemistry
  • HIV Antigens / immunology
  • HIV Infections / immunology*
  • HIV Infections / therapy
  • HIV Infections / virology*
  • HIV-1 / immunology*
  • Host-Pathogen Interactions / immunology
  • Humans
  • Immunologic Surveillance
  • Immunotherapy, Adoptive* / methods
  • Protein Binding
  • Receptors, Antigen, T-Cell / genetics
  • Receptors, Antigen, T-Cell / metabolism*
  • Receptors, Chimeric Antigen / genetics
  • Receptors, Chimeric Antigen / metabolism
  • Structure-Activity Relationship
  • T-Lymphocytes / immunology*
  • T-Lymphocytes / metabolism*
  • Virus Latency / immunology

Substances

  • HIV Antigens
  • Receptors, Antigen, T-Cell
  • Receptors, Chimeric Antigen