Lymph node migratory dendritic cells modulate HIV-1 transcription through PD-1 engagement

PLoS Pathog. 2019 Jul 22;15(7):e1007918. doi: 10.1371/journal.ppat.1007918. eCollection 2019 Jul.

Abstract

T-follicular helper (Tfh) cells, co-expressing PD-1 and TIGIT, serve as a major cell reservoir for HIV-1 and are responsible for active and persistent HIV-1 transcription after prolonged antiretroviral therapy (ART). However, the precise mechanisms regulating HIV-1 transcription in lymph nodes (LNs) remain unclear. In the present study, we investigated the potential role of immune checkpoint (IC)/IC-Ligand (IC-L) interactions on HIV-1 transcription in LN-microenvironment. We show that PD-L1 (PD-1-ligand) and CD155 (TIGIT-ligand) are predominantly co-expressed on LN migratory (CD1chighCCR7+CD127+) dendritic cells (DCs), that locate predominantly in extra-follicular areas in ART treated individuals. We demonstrate that TCR-mediated HIV production is suppressed in vitro in the presence of recombinant PD-L1 or CD155 and, more importantly, when LN migratory DCs are co-cultured with PD-1+/Tfh cells. These results indicate that LN migratory DCs expressing IC-Ls may more efficiently restrict HIV-1 transcription in the extra-follicular areas and explain the persistence of HIV transcription in PD-1+/Tfh cells after prolonged ART within germinal centers.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-HIV Agents / therapeutic use
  • Antibodies, Monoclonal, Humanized / administration & dosage
  • Cell Movement / immunology
  • Cellular Microenvironment / immunology
  • Coculture Techniques
  • Dendritic Cells / immunology
  • Dendritic Cells / virology
  • Germinal Center / immunology
  • Germinal Center / virology
  • HIV Infections / drug therapy
  • HIV Infections / immunology*
  • HIV Infections / virology*
  • HIV-1 / genetics*
  • HIV-1 / immunology
  • HIV-1 / pathogenicity*
  • Host Microbial Interactions / immunology
  • Humans
  • In Vitro Techniques
  • Lymph Nodes / immunology
  • Lymph Nodes / virology
  • Programmed Cell Death 1 Ligand 2 Protein / metabolism
  • Programmed Cell Death 1 Receptor / antagonists & inhibitors
  • Programmed Cell Death 1 Receptor / metabolism*
  • Receptors, Immunologic / metabolism
  • Receptors, Virus / metabolism
  • T-Lymphocytes, Helper-Inducer / immunology
  • T-Lymphocytes, Helper-Inducer / virology
  • Transcription, Genetic
  • Virulence

Substances

  • Anti-HIV Agents
  • Antibodies, Monoclonal, Humanized
  • PDCD1 protein, human
  • PDCD1LG2 protein, human
  • Programmed Cell Death 1 Ligand 2 Protein
  • Programmed Cell Death 1 Receptor
  • Receptors, Immunologic
  • Receptors, Virus
  • TIGIT protein, human
  • poliovirus receptor
  • pembrolizumab