Evidence map›Paper›PMID 25072116›Full record

ReviewImmunology letters2014

Targeting human dendritic cells in situ to improve vaccines.

Kartik Sehgal, Kavita M Dhodapkar, Madhav V Dhodapkar

Abstract readReview
In one paragraph

Review in Immunology letters, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing 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

50 citing papers in PubMed.

  1. Review
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  14. Self-assembled polymeric micelle as a novel mRNA delivery carrier.Journal of controlled release : official journal of the Controlled Release Society · 2021
    Article
  15. Article
  16. Article
  17. Article
  18. Influenza Virus and SARS-CoV-2 Vaccines.Journal of immunology (Baltimore, Md. : 1950) · 2021
    Review
  19. Review
  20. Review
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

3 authors.

Kartik SehgalDepartment of Medicine, Yale University, New Haven, CT, United States.
Kavita M DhodapkarPediatrics, Yale University, New Haven, CT, United States.
Madhav V DhodapkarDepartment of Medicine, Yale University, New Haven, CT, United States. Electronic address: madhav.dhodapkar@yale.edu.

Funding

Understanding Hemotopoietic Neoplasias using Humanized MiceR01CA156689 · NCI · YALE UNIVERSITY · PI DHODAPKAR, MADHAV V, FLAVELL, RICHARD A · 2010 to 2014
$5.0M
Anti-Tumor immunity in myelomaR01CA106802 · NCI · YALE UNIVERSITY · PI DHODAPKAR, MADHAV V · 2004 to 2016
$3.3M
Fcgamma mediated regulation of dendritic cell functionR01AI079222 · NIAID · YALE UNIVERSITY · PI DHODAPKAR, KAVITA MADHAV · 2009 to 2012
$1.6M
Targeting myeloma via dendritic cellsR01CA109465 · NCI · YALE UNIVERSITY · PI DHODAPKAR, MADHAV V · 2005 to 2009
$1.6M
Immunity to stem cell antigens in preneoplastic gammopathyR01CA135110 · NCI · YALE UNIVERSITY · PI DHODAPKAR, MADHAV V · 2008 to 2013
$1.6M
NCI NIH HHS CA106802NCI NIH HHS CA135110NCI NIH HHS R01 CA106802NCI NIH HHS R01 CA109465NCI NIH HHS R01 CA135110NCI NIH HHS R01 CA156689NIAID NIH HHS AI079222NIAID NIH HHS R01 AI079222
6 · The paper itself

Abstract

Dendritic cells (DCs) provide a critical link between innate and adaptive immunity. The potent antigen presenting properties of DCs makes them a valuable target for the delivery of immunogenic cargo. Recent clinical studies describing in situ DC targeting with antibody-mediated targeting of DC receptor through DEC-205 provide new opportunities for the clinical application of DC-targeted vaccines. Further advances with nanoparticle vectors which can encapsulate antigens and adjuvants within the same compartment and be targeted against diverse DC subsets also represent an attractive strategy for targeting DCs. This review provides a brief summary of the rationale behind targeting dendritic cells in situ, the existing pre-clinical and clinical data on these vaccines and challenges faced by the next generation DC-targeted vaccines.

Indexed as

AnimalsAntibodiesAntigen PresentationAntigen-Presenting CellsAntigensDendritic CellsHumansMiceNanoparticlesPhenotypeVaccinesAntibodiesAntigensVaccinesDendritic cellNanoparticlesTargeted vaccines

Identifiers

PMID25072116
PMCPMC4506641

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.