Evidence map›Paper›PMID 23039887›Full record

ArticleClinical and experimental immunology2012

Optimizing dendritic cell vaccine for immunotherapy in multiple myeloma: tumour lysates are more potent tumour antigens than idiotype protein to promote anti-tumour immunity.

S Hong, H Li, J Qian, J Yang, Y Lu, Q Yi

Open access · greenAbstract read
In one paragraph

Article in Clinical and experimental immunology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

26 citing papers in PubMed, 40 citations in OpenAlex.

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  15. Dendritic Cell Therapies for Hematologic Malignancies.Molecular therapy. Methods & clinical development · 2017
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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

6 authors at 1 institution in 1 country.

S HongDepartment of Lymphoma/Myeloma, Division of Cancer Medicine, and Center for Cancer Immunology Research, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
H Li
J Qian
J Yang
Y Lu
Q Yi
The University of Texas MD Anderson Cancer Center · US

Funding

U OF TEXAS HLTH SCI CTR HOUSTON CENTER FOR CLINICAL AND TRANSLATIONAL SCIENCESUL1RR024148 · NCRR · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI MCPHERSON, DAVID D · 2006 to 2010
$27.9M
P4 -TARGETING MULTIPLE MYELOMA BY COMBINING CDK INHIBITORS AND BCL-2 ANTAGONISTSP50CA142509 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI KWAK, LARRY W · 2010 to 2014
$11.1M
Targeting Plasmacytoid Dendritic Cells to Treat Human MyelomaR01CA163881 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI YI, QING · 2012 to 2016
$2.0M
C-reactive protein promotes myeloma cell-mediated bone destructionR01CA138398 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI YI, QING · 2010 to 2014
$1.6M
Idiotype-specific effector T cells in multiple myelomaR01CA096569 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI YI, QING · 2002 to 2006
$1.5M
Optimizing Dendritic Cell Immunotherapy in MyelomaR01CA103978 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI YI, QING · 2004 to 2008
$1.4M
Targeting surface b2M for myeloma and bone therapyR01CA138402 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI YI, QING · 2009 to 2013
$1.3M
NCI NIH HHS CA103978NCI NIH HHS CA138398NCI NIH HHS CA138402NCI NIH HHS CA96569NCI NIH HHS P50 CA142509NCI NIH HHS R01 CA096569NCI NIH HHS R01 CA103978NCI NIH HHS R01 CA138398NCI NIH HHS R01 CA138402NCI NIH HHS R01 CA163881NCRR NIH HHS UL1 RR024148
6 · The paper itself

Abstract

Dendritic cells (DCs) are the most potent antigen-presenting cells and are the mediators of T cell immunity. Many investigators have explored the potential of using DCs as a vaccine for tumour-derived antigens in immunotherapy of B cell malignancies, and the results have been disappointing. To search for better tumour antigens to improve the efficacy of DC-based immunotherapy in myeloma, we evaluated and compared the efficacy of the vaccination of DCs pulsed with idiotype (Id) or tumour lysate in the 5TGM1 myeloma mouse model. Our results showed that Id- or tumour lysate-pulsed DC vaccines protected mice efficiently against developing myeloma, retarded tumour growth, induced tumour regression against established tumour and protected surviving mice from tumour rechallenge. The therapeutic responses were associated with an induction of strong humoral immune responses, including anti-Id or anti-lysate antibodies, and cellular immune responses including myeloma-specific CD8(+) cytotoxic T lymphocytes, CD4(+) type 1 T helper cells and memory T cells in mice receiving Id- or tumour lysate-pulsed DC vaccines. In addition, our studies showed that tumour lysate-pulsed DCs were more potent vaccines than the Id-pulsed DC vaccines to promote anti-tumour immunity in the model. This information will be important for improving the strategies of DC-based immunotherapy for patients with myeloma and other B cell tumours.

Indexed as

AnimalsAntigens, NeoplasmB-LymphocytesCancer VaccinesCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCell Line, TumorDendritic CellsImmunity, CellularImmunity, HumoralImmunoglobulin IdiotypesImmunotherapyInterferon-gammaMiceMice, Inbred C57BLMultiple MyelomaAntigens, NeoplasmCancer VaccinesImmunoglobulin IdiotypesInterferon-gamma

Identifiers

PMID23039887
PMCPMC3482363
OpenAlexW1580607762

What OpenQuestion holds

Textmetadata
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.