Evidence map›Paper›PMID 31498845›Full record

ArticlePLoS pathogens2019

Anti-HIV potency of T-cell responses elicited by dendritic cell therapeutic vaccination.

Mathieu Surenaud, Monica Montes, Cecilia S Lindestam Arlehamn, Alessandro Sette, Jacques Banchereau, Karolina Palucka, Jean-Daniel Lelièvre, Christine Lacabaratz, Yves Lévy

Abstract readClinical Trial, Phase I
In one paragraph

Article in PLoS pathogens, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed.

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  15. Therapeutic Vaccines for the Treatment of HIV.Translational research : the journal of laboratory and clinical medicine · 2020
    Review
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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

9 authors.

Mathieu SurenaudVaccine Research Institute, INSERM U955-Université Paris-Est Créteil, Créteil, France.ORCID 0000-0002-3312-7871
Monica MontesBaylor Institute for Immunology Research, Center for Human Vaccines, Dallas TX, United States of America.
Cecilia S Lindestam ArlehamnLa Jolla Institute for Immunology, Department of Vaccine Discovery, La Jolla, California, United States of America.ORCID 0000-0001-7302-8002
Alessandro SetteLa Jolla Institute for Immunology, Department of Vaccine Discovery, La Jolla, California, United States of America.
Jacques BanchereauBaylor Institute for Immunology Research, Center for Human Vaccines, Dallas TX, United States of America.
Karolina PaluckaBaylor Institute for Immunology Research, Center for Human Vaccines, Dallas TX, United States of America.
Jean-Daniel LelièvreVaccine Research Institute, INSERM U955-Université Paris-Est Créteil, Créteil, France.ORCID 0000-0002-8182-3628
Christine LacabaratzVaccine Research Institute, INSERM U955-Université Paris-Est Créteil, Créteil, France.ORCID 0000-0001-6925-0225
Yves LévyVaccine Research Institute, INSERM U955-Université Paris-Est Créteil, Créteil, France.ORCID 0000-0002-5549-6256

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Identification and characterization of CD8+ and CD4+ T-cell epitopes elicited by HIV therapeutic vaccination is key for elucidating the nature of protective cellular responses and mechanism of the immune evasion of HIV. Here, we report the characterization of HIV-specific T-cell responses in cART (combination antiretroviral therapy) treated HIV-1 infected patients after vaccination with ex vivo-generated IFNα Dendritic Cells (DCs) loaded with LIPO-5 (HIV-1 Nef 66-97, Nef 116-145, Gag 17-35, Gag 253-284 and Pol 325-355 lipopeptides). Vaccination induced and/or expanded HIV-specific CD8+ T cells producing IFNγ, perforin, granzyme A and granzyme B, and also CD4+ T cells secreting IFNγ, IL-2 and IL-13. These responses were directed against dominant and subdominant epitopes representing all vaccine regions; Gag, Pol and Nef. Interestingly, IL-2 and IL-13 produced by CD4+ T cells were negatively correlated with the peak of viral replication following analytic treatment interruption (ATI). Epitope mapping confirmed that vaccination elicited responses against predicted T-cell epitopes, but also allowed to identify a set of 8 new HIV-1 HLA-DR-restricted CD4+ T-cell epitopes. These results may help to better design future DC therapeutic vaccines and underscore the role of vaccine-elicited CD4+ T-cell responses to achieve control of HIV replication.

Indexed as

AdultAIDS VaccinesAnti-Retroviral AgentsAntiviral AgentsCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesDendritic CellsDrug Therapy, CombinationEpitopesEpitopes, T-LymphocyteFemaleHIV-1HIV InfectionsHumansInterferon-alphaMaleAIDS VaccinesAnti-Retroviral AgentsAntiviral AgentsEpitopesEpitopes, T-LymphocyteInterferon-alpha

Identifiers

PMID31498845
PMCPMC6733439

What OpenQuestion 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 OpenQuestion graph.