Evidence map›Paper›PMID 22126373›Full record

ReviewJournal of internal medicine2012

Dendritic cell-targeted protein vaccines: a novel approach to induce T-cell immunity.

C Trumpfheller, M P Longhi, M Caskey, J Idoyaga, L Bozzacco, T Keler, S J Schlesinger, R M Steinman

Registry-linked trialOpen access · bronzeAbstract readReview
In one paragraph

Review in Journal of internal medicine, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02071095 (Simultaneous Disruption of Latency and Immune Enhancement by Poly-ICLC During HIV-1 Infection), which is not on this map. Cited by 87 papers.

0numbers the graph read from it
0cells of the map it votes in
87citing papers in PubMed
8.8field-weighted citation impact, top 2% 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.

NCT02071095 phase1 / phase2completednot on this mapstarted 2014, after this paper: background citation

Simultaneous Disruption of Latency and Immune Enhancement by Poly-ICLC During HIV-1 Infection

TypeinterventionalSponsorNina BhardwajRan2014 to 2016Enrolled15ConditionsHIV-1 Infected Adults With Chronic HIV-1 InfectionArmsArm A: Poly-ICLC, Arm B: Normal Saline
3 · Its place in the literature

Who cites it

87 citing papers in PubMed, 160 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Review
  9. Review
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  11. Review
  12. Article
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  14. Review
  15. Review
  16. COVID-19 vaccine platforms: Delivering on a promise?Human vaccines & immunotherapeutics · 2021
    Review
  17. Review
  18. Article
  19. IL-10 Signaling in the Tumor Microenvironment of Ovarian Cancer.Advances in experimental medicine and biology · 2021
    Review
  20. Article

27 more citing papers are in PubMed but not listed here.

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

8 authors at 2 institutions in 1 country.

C TrumpfhellerLaboratory of Cellular Physiology and Immunology and Chris Browne Center for Immunology and Immune Diseases, The Rockefeller University, New York, NY 10065, USA. trumpfc@mail.rockefeller.edu
M P Longhi
M Caskey
J Idoyaga
L Bozzacco
T Keler
S J Schlesinger
R M Steinman
Rockefeller University · USCelldex Therapeutics (United States) · US

Funding

TRANSFORMING TRANSLATIONAL SCIENCE AND EDUCATION TO BENEFIT HUMAN HEALTHUL1RR024143 · NCRR · ROCKEFELLER UNIVERSITY · PI COLLER, BARRY · 2006 to 2011
$49.1M
Protein Expression CoreP01AI081677 · NIAID · ROCKEFELLER UNIVERSITY · PI NUSSENZWEIG, MICHEL C · 2009 to 2013
$10.6M
Characterization of the immunity induced by a DEC205-targeted HIV vaccineK23AI084855 · NIAID · ROCKEFELLER UNIVERSITY · PI CASKEY, MARINA · 2009 to 2013
$686k
NCRR NIH HHS UL1 RR024143NCRR NIH HHS UL1RR024143NIAID NIH HHS AI081677NIAID NIH HHS K23 AI084855NIAID NIH HHS K23AI084855NIAID NIH HHS P01 AI081677
6 · The paper itself

Abstract

Current vaccines primarily work by inducing protective antibodies. However, in many infections like HIV, malaria and tuberculosis as well as cancers, there remains a need for durable and protective T-cell immunity. Here, we summarize our efforts to develop a safe T-cell-based protein vaccine that exploits the pivotal role of dendritic cells (DC) in initiating adaptive immunity. Focusing on HIV, gag-p24 protein antigen is introduced into a monoclonal antibody (mAb) that efficiently and specifically targets the DEC-205 antigen uptake receptor on DC. When administered together with synthetic double-stranded RNA, polyriboinosinic:polyribocytidylic acid (poly IC) or its analogue poly IC stabilized with carboxymethylcellulose and poly-L-lysine (poly ICLC), as adjuvant, HIV gag-p24 within anti-DEC-205 mAb is highly immunogenic in mice, rhesus macaques, and in ongoing research, healthy human volunteers. Human subjects form both T- and B-cell responses to DC-targeted protein. Thus, DC-targeted protein vaccines are a potential new vaccine platform, either alone or in combination with highly attenuated viral vectors, to induce integrated immune responses against microbial or cancer antigens, with improved ease of manufacturing and clinical use.

Indexed as

Adjuvants, ImmunologicAnimalsAntigens, CDCarboxymethylcellulose SodiumCD8-Positive T-LymphocytesDendritic CellsGene Products, gagHumansImmunity, CellularInterferon InducersLectins, C-TypeMiceMinor Histocompatibility AntigensPoly I-CPolylysineReceptors, Cell SurfaceAdjuvants, ImmunologicAntigens, CDCarboxymethylcellulose SodiumDEC-205 receptorGene Products, gagInterferon InducersLectins, C-TypeMinor Histocompatibility AntigensPoly I-Cpoly ICLCPolylysineReceptors, Cell SurfaceToll-Like ReceptorsVaccines

Identifiers

PMID22126373
PMCPMC3261312
OpenAlexW1732892700

What OpenQuestion holds

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LicenceTDM
Read underepoch 390

Registered trials

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.