Evidence map›Paper›PMID 25888530›Full record

ArticleJournal of hematology & oncology2015

A novel vaccine for mantle cell lymphoma based on targeting cyclin D1 to dendritic cells via CD40.

Jingtao Chen, Gerard Zurawski, Sandy Zurawski, Zhiqing Wang, Keiko Akagawa, Sangkon Oh, Ueno Hideki, Joseph Fay, Jacques Banchereau, Wenru Song and 1 more

Open access · goldAbstract read
In one paragraph

Article in Journal of hematology & oncology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

11 citing papers in PubMed, 17 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

11 authors at 3 institutions in 2 countries.

Jingtao ChenInstitute of Translational Medicine, the First Hospital, Jilin University, Changchun, 130031, China. jtchen@jlu.edu.cn.
Gerard ZurawskiBaylor Institute for Immunology Research and Sammons Cancer Center, Dallas, TX, 75204, USA. gerardz@baylorhealth.edu.
Sandy ZurawskiBaylor Institute for Immunology Research and Sammons Cancer Center, Dallas, TX, 75204, USA. sandyz@baylorhealth.edu.
Zhiqing WangBaylor Institute for Immunology Research and Sammons Cancer Center, Dallas, TX, 75204, USA. zhiqingw@baylorhealth.edu.
Keiko AkagawaBaylor Institute for Immunology Research and Sammons Cancer Center, Dallas, TX, 75204, USA. rbg599@gmail.com.
Sangkon OhBaylor Institute for Immunology Research and Sammons Cancer Center, Dallas, TX, 75204, USA. sangkono@baylorhealth.edu.
Ueno HidekiBaylor Institute for Immunology Research and Sammons Cancer Center, Dallas, TX, 75204, USA. hidekiu@baylorhealth.edu.
Joseph FayBaylor Institute for Immunology Research and Sammons Cancer Center, Dallas, TX, 75204, USA. Joseph.Fay@baylorhealth.edu.
Jacques BanchereauBaylor Institute for Immunology Research and Sammons Cancer Center, Dallas, TX, 75204, USA. Jacque.Banchereau@jax.org.
Wenru SongBaylor Institute for Immunology Research and Sammons Cancer Center, Dallas, TX, 75204, USA. wenru.song@gmail.com.
A Karolina PaluckaBaylor Institute for Immunology Research and Sammons Cancer Center, Dallas, TX, 75204, USA. Karolina.Palucka@jax.org.
Baylor University · USJackson Laboratory · USJilin University · CN

Funding

A Pull-Push Strategy for Lymphoma ImmunotherapyK08CA105064 · NCI · STANFORD UNIVERSITY · PI SONG, WENRU · 2004 to 2008
$643k
NCI NIH HHS K08 CA105064
6 · The paper itself

Abstract

backgroundMantle cell lymphoma (MCL) is a distinct clinical pathologic subtype of B cell non-Hodgkin's lymphoma often associated with poor prognosis. New therapeutic approaches based on boosting anti-tumor immunity are needed. MCL is associated with overexpression of cyclin D1 thus rendering this molecule an interesting target for immunotherapy.

methodsWe show here a novel strategy for the development of recombinant vaccines carrying cyclin D1 cancer antigens that can be targeted to dendritic cells (DCs) via CD40.

resultsHealthy individuals and MCL patients have a broad repertoire of cyclin D1-specific CD4(+) and CD8(+) T cells. Cyclin D1-specific T cells secrete IFN-γ. DCs loaded with whole tumor cells or with selected peptides can elicit cyclin D1-specific CD8(+) T cells that kill MCL tumor cells. We developed a recombinant vaccine based on targeting cyclin D1 antigen to human DCs via an anti-CD40 mAb. Targeting monocyte-derived human DCs in vitro with anti-CD40-cyclin D1 fusion protein expanded a broad repertoire of cyclin D1-specific CD4(+) and CD8(+) T cells.

conclusionsThis study demonstrated that cyclin D1 represents a good target for immunotherapy and targeting cyclin D1 to DCs provides a new strategy for mantle cell lymphoma vaccine.

Indexed as

AgedCancer VaccinesCD40 AntigensCD8-Positive T-LymphocytesCyclin D1Dendritic CellsHumansIn Vitro TechniquesLymphocyte ActivationLymphoma, Mantle-CellMaleMiddle AgedMolecular Targeted TherapyRecombinant Fusion ProteinsVaccines, SyntheticCancer VaccinesCCND1 protein, humanCD40 AntigensCyclin D1Recombinant Fusion ProteinsVaccines, Synthetic

Identifiers

PMID25888530
PMCPMC4424584
OpenAlexW1991044702

What OpenQuestion holds

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LicenceCC BY
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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.