Evidence map›Paper›PMID 23615121›Full record

ArticleAIDS (London, England)2013

Targeting concatenated HIV antigens to human CD40 expands a broad repertoire of multifunctional CD4+ and CD8+ T cells.

Anne-Laure Flamar, Yaming Xue, Sandra M Zurawski, Monica Montes, Bryan King, Louis Sloan, SangKon Oh, Jacques Banchereau, Yves Levy, Gerard Zurawski

Abstract read
In one paragraph

Article in AIDS (London, England), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
2.0field-weighted citation impact, top 14% of its field
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

34 citing papers in PubMed, 46 citations in OpenAlex.

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  10. Anti-CD40 Antibodies Fused to CD40 Ligand Have Superagonist Properties.Journal of immunology (Baltimore, Md. : 1950) · 2021
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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

10 authors at 7 institutions in 3 countries.

Anne-Laure FlamaraBaylor Institute for Immunology Research, Dallas, Texas, USA bANRS HIV Vaccine Network/Vaccine Research Institute, Paris cEcole doctorale Sciences de la Vie et de la Santé, Université Paris-Est, Créteil, France dINSERM U899 eNorth Texas Infectious Diseases, Dallas, Texas, USA fUniversité Paris-Est, Faculté de Médecine, INSERM U955 gAssistance Publique-Hôpitaux de Paris, Groupe Henri-Mondor Albert-Chenevier, service d'immunologie clinique, Créteil, France.
Yaming Xue
Sandra M Zurawski
Monica Montes
Bryan King
Louis Sloan
SangKon Oh
Jacques Banchereau
Yves Levy
Gerard Zurawski
Institut National de Recherche en Santé Publique · MLTexas Center for Infectious Disease · USAllergy, Asthma and Clinical Research Center · USBaylor University Medical Center · USHôpital Albert-Chenevier · FRInserm · FRUniversité Paris Cité · FR

Funding

Targeting Dendritic Cells for Enhanced Musocal ImmunityU19AI057234 · NIAID · BAYLOR RESEARCH INSTITUTE · PI LEGRAND, ROGER · 2003 to 2013
$49.2M
NIAID NIH HHS U19 AI057234NIAID NIH HHS U19 AI-57234
6 · The paper itself

Abstract

objectiveTargeting HIV antigens directly to dendritic cells using monoclonal antibodies against cell-surface receptors has been shown to evoke potent cellular immunity in animal models. The objective of this study was to configure an anti-human CD40 antibody fused to a string of five highly conserved CD4 and CD8 T-cell epitope-rich regions of HIV-1 Gag, Nef and Pol (αCD40.HIV5pep), and then to demonstrate the capacity of this candidate therapeutic vaccine to target these HIV peptide antigens to human dendritic cells to expand functional HIV-specific T cells.

methodsAntigen-specific cytokine production using intracellular flow cytometry and multiplex bead-based assay, and suppression of viral inhibition, were used to characterize the T cells expanded by αCD40.HIV5pep from HIV-infected patient peripheral blood mononuclear cell (PBMC) and dendritic cell/T-cell co-cultures.

resultsThis candidate vaccine expands memory CD4 and CD8 T cells specific to multiple epitopes within all five peptide regions across a wide range of major histocompatibility complex (MHC) haplotypes from HIV-infected patient PBMC and dendritic cell/T-cell co-cultures. These in vitro expanded HIV antigen-specific CD4 and CD8 T cells produce multiple cytokines and chemokines. αCD40.HIV5pep-expanded CD8 T cells have characteristics of cytotoxic effector cells and are able to kill autologous target cells and suppress HIV-1 replication in vitro.

conclusionOur data demonstrate the therapeutic potential of this CD40-targeting HIV candidate vaccine in inducing a broad repertoire of multifunctional T cells in patients.

Indexed as

AIDS VaccinesAntibodies, MonoclonalCD40 AntigensCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCell ProliferationCoculture TechniquesDendritic CellsHIV-1HIV AntigensHumansRecombinant Fusion ProteinsAIDS VaccinesAntibodies, MonoclonalCD40 AntigensHIV AntigensRecombinant Fusion Proteins

Identifiers

PMID23615121
PMCPMC3859846
OpenAlexW2047171958

What OpenQuestion holds

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Registered trials

None linked

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.