Evidence map›Paper›PMID 10974024›Full record

ArticleThe Journal of clinical investigation2000

Detection of a potent humoral response associated with immune-induced remission of chronic myelogenous leukemia.

C J Wu, X F Yang, S McLaughlin, D Neuberg, C Canning, B Stein, E P Alyea, R J Soiffer, G Dranoff, J Ritz

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing 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

47 citing papers in PubMed, 131 citations in OpenAlex.

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  15. Angiogenic cytokines are antibody targets during graft-versus-leukemia reactions.Clinical cancer research : an official journal of the American Association for Cancer Research · 2015
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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

10 authors at 3 institutions in 1 country.

C J WuCenter for Hematologic Oncology, and. Department of Biostatistical Science, Dana-Farber Cancer Institute, and. Department of Medicine, and Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
X F Yang
S McLaughlin
D Neuberg
C Canning
B Stein
E P Alyea
R J Soiffer
G Dranoff
J Ritz
Brigham and Women's Hospital · USHarvard University · USDana-Farber Cancer Institute · US

Funding

Reconstitution of Regulatory T Cells after Allogeneic Stem Cell TransplantationU19AI029530 · NIAID · DANA-FARBER CANCER INSTITUTE · PI SOIFFER, ROBERT JON · 2005 to 2010
$9.0M
T CELL NEOGENESIS AFTER STEM CELL TRANSPLANTATIONP01AI029530 · NIAID · DANA-FARBER CANCER INSTITUTE · PI RITZ, JEROME · 1990 to 2003
$4.5M
NIAID NIH HHS AI-29530NIAID NIH HHS P01 AI029530NIAID NIH HHS U19 AI029530
6 · The paper itself

Abstract

The effectiveness of donor-lymphocyte infusion (DLI) for treatment of relapsed chronic myelogenous leukemia (CML) after allogeneic bone marrow transplantation is a clear demonstration of the graft-versus-leukemia (GVL) effect. T cells are critical mediators of GVL, but the antigenic targets of this response are unknown. To determine whether patients who respond to DLI also develop B-cell immunity to CML-associated antigens, we analyzed sera from three patients with relapsed CML who achieved a complete molecular remission after infusion of donor T cells. Sera from these individuals recognized 13 distinct gene products represented in a CML-derived cDNA library. Two proteins, Jkappa-recombination signal-binding protein (RBP-Jkappa) and related adhesion focal tyrosine kinase (RAFTK), were recognized by sera from three of 19 DLI responders. None of these antigens were recognized by sera from healthy donors or patients with chronic graft-versus-host disease. Four gene products were recognized by sera from CML patients treated with hydroxyurea and nine were detected by sera from CML patients who responded to IFN-alpha. Antibody titers specific for RAFTK, but not for RBP-Jkappa, were found to be temporally associated with the response to DLI. These results demonstrate that patients who respond to DLI generate potent antibody responses to CML-associated antigens, suggesting the development of coordinated T- and B-cell immunity. The characterization of B cell-defined antigens may help identify clinically relevant targets of the GVL response in vivo.

Indexed as

Graft vs Leukemia EffectLymphocyte TransfusionNuclear ProteinsAntibodies, NeoplasmB-LymphocytesDNA-Binding ProteinsFocal Adhesion Kinase 2Gene LibraryHumansImmunoglobulin J Recombination Signal Sequence-Binding ProteinLeukemia, Myelogenous, Chronic, BCR-ABL PositiveMolecular Sequence DataProtein-Tyrosine KinasesRemission InductionSequence Analysis, DNAT-LymphocytesAntibodies, NeoplasmDNA-Binding ProteinsFocal Adhesion Kinase 2Immunoglobulin J Recombination Signal Sequence-Binding ProteinNuclear ProteinsProtein-Tyrosine KinasesRBPJ protein, human

Identifiers

PMID10974024
PMCPMC381287
OpenAlexW2157154499

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.