Evidence map›Paper›PMID 40949488›Full record

ArticleMedComm2025

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

Joana Vitallé, Sara Bachiller, Beatriz Dominguez-Molina, Eirini Moysi, Sara Ferrando-Martínez, María Inés Camacho-Sojo, Isabel Gallego, Alberto Pérez-Gómez, María Reyes Jiménez-Leon, Carmen Gasca-Capote and 8 more

Abstract read
In one paragraph

Article in MedComm, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

18 authors.

Joana VitalléInstitute of Biomedicine of Seville, IBiS/Virgen Del Rocío University Hospital/CSIC/University of Seville Clinical Unit of Infectious Diseases, Microbiology and Parasitology Seville Spain.
Sara BachillerInstitute of Biomedicine of Seville, IBiS/Virgen Del Rocío University Hospital/CSIC/University of Seville Clinical Unit of Infectious Diseases, Microbiology and Parasitology Seville Spain.ORCID https://orcid.org/0000-0002-9000-3787
Beatriz Dominguez-MolinaInstitute of Biomedicine of Seville, IBiS/Virgen Del Rocío University Hospital/CSIC/University of Seville Clinical Unit of Infectious Diseases, Microbiology and Parasitology Seville Spain.
Eirini MoysiTissue Analysis Core Immunology Laboratory Vaccine Research Center NIAID NIH Bethesda Maryland USA.
Sara Ferrando-MartínezTissue Analysis Core Immunology Laboratory Vaccine Research Center NIAID NIH Bethesda Maryland USA.
María Inés Camacho-SojoInstitute of Biomedicine of Seville, IBiS/Virgen Del Rocío University Hospital/CSIC/University of Seville Clinical Unit of Infectious Diseases, Microbiology and Parasitology Seville Spain.
Isabel GallegoInstitute of Biomedicine of Seville, IBiS/Virgen Del Rocío University Hospital/CSIC/University of Seville Clinical Unit of Infectious Diseases, Microbiology and Parasitology Seville Spain.
Alberto Pérez-GómezInstitute of Biomedicine of Seville, IBiS/Virgen Del Rocío University Hospital/CSIC/University of Seville Clinical Unit of Infectious Diseases, Microbiology and Parasitology Seville Spain.ORCID https://orcid.org/0000-0002-3644-2914
María Reyes Jiménez-LeonInstitute of Biomedicine of Seville, IBiS/Virgen Del Rocío University Hospital/CSIC/University of Seville Clinical Unit of Infectious Diseases, Microbiology and Parasitology Seville Spain.
Carmen Gasca-CapoteInstitute of Biomedicine of Seville, IBiS/Virgen Del Rocío University Hospital/CSIC/University of Seville Clinical Unit of Infectious Diseases, Microbiology and Parasitology Seville Spain.
Francisco José OstosInstitute of Biomedicine of Seville, IBiS/Virgen Del Rocío University Hospital/CSIC/University of Seville Clinical Unit of Infectious Diseases, Microbiology and Parasitology Seville Spain.
Mohammed Rafii-El-Idrissi BenhniaInstitute of Biomedicine of Seville, IBiS/Virgen Del Rocío University Hospital/CSIC/University of Seville Clinical Unit of Infectious Diseases, Microbiology and Parasitology Seville Spain.
Laura E ViaTuberculosis Research Section Laboratory of Clinical Immunology and Microbiology, and Tuberculosis Imaging Program Division of Intramural Research NIAID NIH Bethesda Maryland USA.
Antonio MochónOtorhinolaryngology Service Virgen Del Rocío University Hospital Seville Spain.
Luis Fernando López-CortesInstitute of Biomedicine of Seville, IBiS/Virgen Del Rocío University Hospital/CSIC/University of Seville Clinical Unit of Infectious Diseases, Microbiology and Parasitology Seville Spain.
Constantinos PetrovasTissue Analysis Core Immunology Laboratory Vaccine Research Center NIAID NIH Bethesda Maryland USA.
Richard A KoupTissue Analysis Core Immunology Laboratory Vaccine Research Center NIAID NIH Bethesda Maryland USA.
Ezequiel Ruiz-MateosInstitute of Biomedicine of Seville, IBiS/Virgen Del Rocío University Hospital/CSIC/University of Seville Clinical Unit of Infectious Diseases, Microbiology and Parasitology Seville Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

CD141 myeloid DCCD8 T celldendritic cell (DC)HIVlymph nodeplasmacytoid DC

Identifiers

PMID40949488
PMCPMC12426486

What Socratic holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.