Plasmacytoid and CD141+ Myeloid Dendritic Cells Cooperation with CD8+ T Cells in Lymph Nodes is Associated with HIV Control

Dendritic cells (DC) are known to modulate antiviral immune responses; however, the knowledge about the role of different DC subsets in antiviral T cell priming in human tissues remains uncompleted. In the context of HIV infection, we determined the phenotype and location of plasmacytoid and CD141+ myeloid DCs (pDCs and mDCs) in lymph nodes of people living with HIV (PLWH). We found an interaction between pDCs and CD141+ mDCs with CD8+ T cells, being associated with participants' viral levels in blood and tissue. Moreover, we demonstrated a higher and more polyfunctional superantigen- and HIV-specific CD8+ T cell response after the coculture with Toll-like receptor (TLR)-primed pDCs and CD141+ mDCs. Last, we showed the potential of programmed cell death-1 (PD-1) blocking using pembrolizumab to further increase antigen-specific CD8+ T cell response along with TLR agonists. Therefore, these results showed a cooperation between pDCs, CD141+ mDCs and CD8+ T cells in lymph nodes of PLWH, which is associated with higher HIV control, highlighting the importance of DC subsets crosstalk to achieve a more potent anti-HIV response and support the use of DC-based immunotherapies for HIV control.

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Publication Details

Journal
MedComm
Published
2025-09-01
DOI
https://doi.org/10.1002/mco2.70354
Primary Topic
Immune Cell Function and Interaction
Type
article
Field-Weighted Citation Impact
0.00

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article

Plasmacytoid and CD141+ Myeloid Dendritic Cells Cooperation with CD8+ T Cells in Lymph Nodes is Associated with HIV Control

Beatriz Domínguez-Molina, Ezequiel Ruíz-Mateos, Laura E. Via, Joana Vitallé et al.
MedComm
Immune Cell Function and Interaction
article

Plasmacytoid and CD141+ Myeloid Dendritic Cells Cooperation with CD8+ T Cells in Lymph Nodes is Associated with HIV Control

Beatriz Domínguez-Molina, Ezequiel Ruíz-Mateos, Laura E. Via, Joana Vitallé, Sara Bachiller, Alberto Pérez‐Gómez, Sara Ferrando‐Martínez, Richard A. Koup, Carmen Gasca‐Capote, Francisco José Ostos, María Reyes Jiménez‐León, Mohammed Rafii‐El‐Idrissi Benhnia, Luís F. López‐Cortés, Asunción Mochón, María Inés Camacho-Sojo, Eirini Moysi, Constantinos Petrovas, Isabel Gallego
article en

Abstract

Dendritic cells (DC) are known to modulate antiviral immune responses; however, the knowledge about the role of different DC subsets in antiviral T cell priming in human tissues remains uncompleted. In the context of HIV infection, we determined the phenotype and location of plasmacytoid and CD141+ myeloid DCs (pDCs and mDCs) in lymph nodes of people living with HIV (PLWH). We found an interaction between pDCs and CD141+ mDCs with CD8+ T cells, being associated with participants' viral levels in blood and tissue. Moreover, we demonstrated a higher and more polyfunctional superantigen- and HIV-specific CD8+ T cell response after the coculture with Toll-like receptor (TLR)-primed pDCs and CD141+ mDCs. Last, we showed the potential of programmed cell death-1 (PD-1) blocking using pembrolizumab to further increase antigen-specific CD8+ T cell response along with TLR agonists. Therefore, these results showed a cooperation between pDCs, CD141+ mDCs and CD8+ T cells in lymph nodes of PLWH, which is associated with higher HIV control, highlighting the importance of DC subsets crosstalk to achieve a more potent anti-HIV response and support the use of DC-based immunotherapies for HIV control.

MedCommVol. 6(9)
National Institutes of Health (US), Instituto de Biomedicina de Sevilla (ES), National Institute of Research in Tuberculosis (IN), Hospital Universitario Virgen del Rocío (ES), Universidad de Sevilla (ES), University of Lausanne (CH)
U.S. Department of Health and Human Services, Gilead Sciences, Universidad de Sevilla, European Commission, Junta de Andalucía, National Institutes of Health, Consejo Superior de Investigaciones Científicas, Instituto de Salud Carlos III, Agencia Estatal de Investigación, National Institute of Allergy and Infectious Diseases
Openalex Percentile: Top 74%
Immune Cell Function and Interaction
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