Evidence map›Paper›PMID 20424114›Full record

ArticleCancer research2010

Combining CD19 redirection and alloanergization to generate tumor-specific human T cells for allogeneic cell therapy of B-cell malignancies.

Jeff K Davies, Harjeet Singh, Helen Huls, Dongin Yuk, Dean A Lee, Partow Kebriaei, Richard E Champlin, Lee M Nadler, Eva C Guinan, Laurence J N Cooper

Open access · bronzeAbstract read
In one paragraph

Article in Cancer research, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

27 citing papers in PubMed, 45 citations in OpenAlex.

  1. Article
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  11. Translational Implications for Off-the-shelf Immune Cells Expressing Chimeric Antigen Receptors.Molecular therapy : the journal of the American Society of Gene Therapy · 2016
    Review
  12. Article
  13. Selective inhibition of tumor growth by clonal NK cells expressing an ErbB2/HER2-specific chimeric antigen receptor.Molecular therapy : the journal of the American Society of Gene Therapy · 2015
    Article
  14. Article
  15. Article
  16. Review
  17. Sleeping beauty system to redirect T-cell specificity for human applications.Journal of immunotherapy (Hagerstown, Md. : 1997) · 2013
    Article
  18. Review
  19. Article
  20. Article
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

10 authors at 3 institutions in 1 country.

Jeff K DaviesDepartment of Medical Oncology, Dana-Farber Cancer Institute, Children's Hospital, Boston, Massachusetts, USA.
Harjeet Singh
Helen Huls
Dongin Yuk
Dean A Lee
Partow Kebriaei
Richard E Champlin
Lee M Nadler
Eva C Guinan
Laurence J N Cooper
Dana-Farber Cancer Institute · USThe University of Texas MD Anderson Cancer Center · USBoston Children's Hospital · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Vanessa Jensen · 1985 to 2026
$290.8M
Specific Control of donor Anti-host AlloreactiviyU19CA100265 · NCI · DANA-FARBER CANCER INST · PI NADLER, LEE MARSHALL · 2006 to 2008
$10.3M
Rebuilding Immunity for SurvivalP01CA100265 · NCI · DANA-FARBER CANCER INSTITUTE · PI NADLER, LEE MARSHALL · 2003 to 2005
$7.2M
Adoptive immunotherapy after umbilical cord blood transplantR01CA124782 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI COOPER, LAURENCE J.N. · 2007 to 2011
$2.0M
T-cell Therapy for B-lineage Acute Lymphoblastic LeukemiaR01CA141303 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI COOPER, LAURENCE J.N. · 2010 to 2014
$1.5M
Enhancing the efficacy of CD19-specific cord blood-derived T CellsR01CA120956 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI COOPER, LAURENCE J.N. · 2007 to 2011
$1.5M
UCB-DERIVED CD19-SPECIFIC T CELLS FOR UNIVERSAL TREATMENT OF B-CELL MALIGNANCYR33CA116127 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI COOPER, LAURENCE J.N. · 2010 to 2011
$1.4M
Ex Vivo Alloanergization to Improve Immunity After Haploidentical TransplantR21CA137645 · NCI · DANA-FARBER CANCER INST · PI GUINAN, EVA C · 2009 to 2010
$745k
UCB-DERIVED CD19-SPECIFIC T CELLS FOR UNIVERSAL TREATMENT OF B-CELL MALIGNANCYR21CA116127 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI COOPER, LAURENCE J.N. · 2007 to 2008
$371k
Imaging Infused CD19 Specific T Cells in the TumorR21CA129390 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI COOPER, LAURENCE J.N. · 2007 to 2008
$324k
NCI NIH HHS 5P30CA016672-32NCI NIH HHS CA16672NCI NIH HHS P01 CA100265NCI NIH HHS P30 CA016672NCI NIH HHS R01 CA120956NCI NIH HHS R01 CA124782NCI NIH HHS R01 CA141303NCI NIH HHS R01S CA120956NCI NIH HHS R01S CA124782NCI NIH HHS R21 CA116127NCI NIH HHS R21 CA129390NCI NIH HHS R21 CA137645NCI NIH HHS R21S CA116127NCI NIH HHS R21S CA129390NCI NIH HHS R21S CA137645NCI NIH HHS R33 CA116127NCI NIH HHS U19 CA100265
6 · The paper itself

Abstract

Allogeneic hematopoietic stem-cell transplantation can cure some patients with high-risk B-cell malignancies, but disease relapse following transplantation remains a significant problem. One approach that could be used to augment the donor T-cell-mediated antitumor effect is the infusion of allogeneic donor-derived T cells expressing a chimeric antibody receptor (CAR) specific to the B-cell antigen CD19. However, the use of such cells might result in toxicity in the form of graft-versus-host disease mediated by CD19-specific (CD19-CAR) T cells possessing alloreactive endogenous T-cell receptors. We therefore investigated whether nonalloreactive tumor-specific human T cells could be generated from peripheral blood mononuclear cells of healthy donors by the combination of CD19 redirection via CAR expression and subsequent alloanergization by allostimulation and concomitant blockade of CD28-mediated costimulation. Alloanergization of CD19-CAR T cells resulted in efficient and selective reduction of alloresponses in both CD4(+) and CD8(+) T cells, including allospecific proliferation and cytokine secretion. Importantly, T-cell effector functions including CAR-dependent proliferation and specific target cytolysis and cytokine production were retained after alloanergization. Our data support the application of CD19 redirection and subsequent alloanergization to generate allogeneic donor T cells for clinical use possessing increased antitumor activity but limited capacity to mediate graft-versus-host disease. Immunotherapy with such cells could potentially reduce disease relapse after allogeneic transplantation without increasing toxicity, thereby improving the outcome of patients undergoing allogeneic transplantation for high-risk B-cell malignancies.

Indexed as

Cell- and Tissue-Based TherapyClonal AnergyAdultAnimalsAntigens, CD19Burkitt LymphomaFlow CytometryGraft vs Host DiseaseHematopoietic Stem Cell TransplantationHumansLymphocyte ActivationMiceT-LymphocytesAntigens, CD19

Identifiers

PMID20424114
PMCPMC2873153
OpenAlexW2017772144

What OpenQuestion holds

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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.