Evidence map›Paper›PMID 19880489›Full record

ArticleBlood2009

Antibody-mediated B-cell depletion before adoptive immunotherapy with T cells expressing CD20-specific chimeric T-cell receptors facilitates eradication of leukemia in immunocompetent mice.

Scott E James, Nural N Orgun, Thomas F Tedder, Mark J Shlomchik, Michael C Jensen, Yukang Lin, Philip D Greenberg, Oliver W Press

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

42 citing papers in PubMed, 57 citations in OpenAlex.

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  15. In Vivo Murine-Matured Human CD3Molecular 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

8 authors at 4 institutions in 1 country.

Scott E JamesClinical Research, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
Nural N Orgun
Thomas F Tedder
Mark J Shlomchik
Michael C Jensen
Yukang Lin
Philip D Greenberg
Oliver W Press
Fred Hutch Cancer Center · USCity Of Hope National Medical Center · USDuke Medical Center · USYale University · US

Funding

VIRUS-MEDIATED MYELOSUPPRESSIONP01CA018029 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Evan Newell · 1985 to 2026
$128.4M
Supplement - Inflammatory Triggers in B Cell AutoimmunityU19AI056363 · NIAID · DUKE UNIVERSITY · PI ST. CLAIR, EUGENE WILLIAM · 2003 to 2017
$35.3M
THE ROLE OF B CELLS IN LUPUS NEPHRITIS AND VASCULITISR01AR044077 · NIAMS · YALE UNIVERSITY · PI SHLOMCHIK, MARK J · 1997 to 2016
$6.2M
Mechanisms of Murine Turmor Eradication by ImmunotherapyR01CA033084 · NCI · UNIVERSITY OF WASHINGTON · PI GREENBERG, PHILIP D · 1986 to 2017
$5.8M
MS4A Family Members in Health and DiseaseR01CA105001 · NCI · DUKE UNIVERSITY · PI TEDDER, THOMAS F · 2004 to 2008
$1.2M
Anti-CD20 CTL for Therapy of Mantle Cell LymphomaR21CA117131 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI PRESS, OLIVER W. · 2006 to 2007
$581k
NCI NIH HHS CA105001NCI NIH HHS P01 CA018029NCI NIH HHS P01 CA18029NCI NIH HHS R01 CA033084NCI NIH HHS R01 CA105001NCI NIH HHS R01 CA33084NCI NIH HHS R21 CA-117131NCI NIH HHS R21 CA117131NIAID NIH HHS AI56363NIAID NIH HHS U19 AI056363NIAMS NIH HHS R01 AR044077NIAMS NIH HHS R01-AR44077
6 · The paper itself

Abstract

We have established a model of leukemia immunotherapy using T cells expressing chimeric T-cell receptors (cTCRs) targeting the CD20 molecule expressed on normal and neoplastic B cells. After transfer into human CD20 (hCD20) transgenic mice, cTCR(+) T cells showed antigen-specific delayed egress from the lungs, concomitant with T-cell deletion. Few cTCR(+) T cells reached the bone marrow (BM) in hCD20 transgenic mice, precluding effectiveness against leukemia. Anti-hCD20 antibody-mediated B-cell depletion before adoptive T-cell therapy permitted egress of mouse CD20-specific cTCR(+) T cells from the lungs, enhanced T-cell survival, and promoted cTCR(+) T cell-dependent elimination of established mouse CD20(+) leukemia. Furthermore, CD20-specific cTCR(+) T cells eliminated residual B cells refractory to depletion with monoclonal antibodies. These findings suggest that combination of antibody therapy that depletes antigen-expressing normal tissues with adoptive T-cell immunotherapy enhances the ability of cTCR(+) T cells to survive and control tumors.

Indexed as

AnimalsAntibodies, MonoclonalAntigens, CD20B-LymphocytesCD3 ComplexCell Line, TumorCell SurvivalFlow CytometryHumansImmunotherapy, AdoptiveLeukemiaMiceMice, Inbred BALB CMice, TransgenicReceptors, Antigen, T-CellSurvival AnalysisAntibodies, MonoclonalAntigens, CD20CD3 antigen, zeta chainCD3 ComplexReceptors, Antigen, T-Cell

Identifiers

PMID19880489
PMCPMC2798862
OpenAlexW2079430120

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.