Evidence map›Paper›PMID 27076169›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2016

Preconditioning Vaccine Sites for mRNA-Transfected Dendritic Cell Therapy and Antitumor Efficacy.

Kristen A Batich, Adam M Swartz, John H Sampson

Open access · greenAbstract read
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

7 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Cancer Vaccine Immunotherapy with RNA-Loaded Liposomes.International journal of molecular sciences · 2018
    Review
  6. Review
  7. 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 at 2 institutions in 1 country.

Kristen A BatichDuke Brain Tumor Immunotherapy Program, Division of Neurosurgery, Department of Surgery, Duke University Medical Center, DUMC Box 3050, 303 Research Drive, 220 Sands Building, Durham, NC, 27710, USA.
Adam M SwartzDuke Brain Tumor Immunotherapy Program, Division of Neurosurgery, Department of Surgery, Duke University Medical Center, DUMC Box 3050, 303 Research Drive, 220 Sands Building, Durham, NC, 27710, USA.
John H SampsonDuke Brain Tumor Immunotherapy Program, Division of Neurosurgery, Department of Surgery, Duke University Medical Center, DUMC Box 3050, 303 Research Drive, 220 Sands Building, Durham, NC, 27710, USA. john.sampson@duke.edu.
Duke Medical Center · USDuke University Hospital · US

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM007171 · NIGMS · DUKE UNIVERSITY · PI KONTOS, CHRISTOPHER D · 1985 to 2021
$31.2M
ORGANIZATION AND FUNCTIONS OF CELLULAR STRUCTUREST32GM007184 · NIGMS · DUKE UNIVERSITY · PI JINKS-ROBERTSON, SUE · 1985 to 2019
$18.2M
Medical Scientist Training Program Training GrantT32GM145449 · NIGMS · DUKE UNIVERSITY · PI Christopher D Kontos · 2022 to 2026
$6.6M
Enhancing dendritic cell migration to drive potent anti-tumor immune responsesF30CA180411 · NCI · DUKE UNIVERSITY · PI BATICH, KRISTEN · 2013 to 2016
$188k
NCI NIH HHS F30 CA180411NIGMS NIH HHS T32 GM007171NIGMS NIH HHS T32 GM007184NIGMS NIH HHS T32 GM145449
6 · The paper itself

Abstract

Messenger RNA (mRNA)-transfected dendritic cell (DC) vaccines have been shown to be a powerful modality for eliciting antitumor immune responses in mice and humans; however, their application has not been fully optimized since many of the factors that contribute to their efficacy remain poorly understood. Work stemming from our laboratory has recently demonstrated that preconditioning the vaccine site with a recall antigen prior to the administration of a dendritic cell vaccine creates systemic recall responses and resultantly enhances dendritic cell migration to the lymph nodes with improved antitumor efficacy. This chapter describes the generation of murine mRNA-transfected DC vaccines, as well as a method for vaccine site preconditioning with protein antigen formulations that create potent recall responses.

Indexed as

AnimalsBone Marrow CellsCancer VaccinesCell DifferentiationDendritic CellsElectrophoresisFlow CytometryImmunotherapyMiceNeoplasmsPhenotypeRNA, MessengerTranscription, GeneticTransfectionVaccinationCancer VaccinesRNA, MessengerBone marrowDendritic cellsElectroporationIntradermalmRNAPreconditioningProtein antigen formulationTranscription

Identifiers

PMID27076169
PMCPMC5527123
OpenAlexW2420189491

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.