Evidence map›Paper›PMID 33101274›Full record

ArticleFrontiers in immunology2020

Clinical Grade Production of Wilms' Tumor-1 Loaded Cord Blood-Derived Dendritic Cells to Prevent Relapse in Pediatric AML After Cord Blood Transplantation.

Maud Plantinga, Vania Lo Presti, Colin G de Haar, Ester Dünnebach, Alejandro Madrigal, Caroline A Lindemans, Jaap Jan Boelens, Stefan Nierkens

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

9 citing papers in PubMed, 14 citations in OpenAlex.

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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

8 authors at 4 institutions in 3 countries.

Maud PlantingaCenter for Translational Immunology, University Medical Center Utrecht, Utrecht, Netherlands.
Vania Lo PrestiCenter for Translational Immunology, University Medical Center Utrecht, Utrecht, Netherlands.
Colin G de HaarPharmacy Department, Cell Therapy Facility, University Medical Center Utrecht, Utrecht, Netherlands.
Ester DünnebachCenter for Translational Immunology, University Medical Center Utrecht, Utrecht, Netherlands.
Alejandro MadrigalUCL Cancer Institute, Royal Free Hospital, London, United Kingdom.
Caroline A LindemansPrincess Máxima Center for Pediatric Oncology, Blood and Marrow Transplantation Program, Utrecht, Netherlands.
Jaap Jan BoelensStem Cell Transplant and Cellular Therapies, Department of Pediatrics, Memorial Sloan Kettering Cancer Center, New York, NY, United States.
Stefan NierkensCenter for Translational Immunology, University Medical Center Utrecht, Utrecht, Netherlands.
University Medical Center Utrecht · NLMemorial Sloan Kettering Cancer Center · USPrincess Máxima Center · NLUniversity College London · GB

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

Hematopoietic cell transplantation (HCT) is a last resort, potentially curative treatment option for pediatric patients with refractory acute myeloid leukemia (AML). Cord blood transplantation (CBT) results in less relapses and less graft-versus-host disease when compared to other sources. Nevertheless, still more than half of the children die from relapses. We therefore designed a strategy to prevent relapses by inducing anti-AML immunity after CBT, using a CB-derived dendritic cell (CBDC) vaccine generated from CD34+ CB cells from the same graft. We here describe the optimization and validation of good manufacturing practice (GMP)-grade production of the CBDC vaccine. We show the feasibility of expanding low amounts of CD34+ cells in a closed bag system to sufficient DCs per patient for at least three rounds of vaccinations. The CBDCs showed upregulated costimulatory molecules after maturation and showed enhanced CCR7-dependent migration toward CCL19 in a trans-well migrations assay. CBDCs expressed Wilms' tumor 1 (WT1) protein after electroporation with

Indexed as

Antigen PresentationBiomarkersCancer VaccinesCombined Modality TherapyCord Blood Stem Cell TransplantationCytotoxicity, ImmunologicDendritic CellsFetal BloodHumansImmunophenotypingLeukemia, Myeloid, AcuteLymphocyte ActivationLymphocyte Culture Test, MixedPrognosisRecurrenceT-Cell Antigen Receptor SpecificityBiomarkersCancer VaccinesWT1 Proteinscord blooddendritic cellsgood manufacturing practiceimmunotherapytransplantationvaccine

Identifiers

PMID33101274
PMCPMC7546401
OpenAlexW3087933245

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.