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