Evidence map›Paper›PMID 20124481›Full record

ArticleCancer research2010

Serologic markers of effective tumor immunity against chronic lymphocytic leukemia include nonmutated B-cell antigens.

Ovidiu Marina, Ursula Hainz, Melinda A Biernacki, Wandi Zhang, Ann Cai, Jonathan S Duke-Cohan, Fenglong Liu, Vladimir Brusic, Donna Neuberg, Jeffery L Kutok and 5 more

Open access · bronzeAbstract readValidation Study
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 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

32 citing papers in PubMed, 39 citations in OpenAlex.

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  9. Alternative splicing of transposable elements in human breast cancer.bioRxiv : the preprint server for biology · 2024
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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

15 authors at 5 institutions in 1 country.

Ovidiu MarinaCancer Vaccine Center and Departments of Medical Oncology and Biostatistics and Computational Biology, Dana-Farber Cancer Institute, Boston, Massachusetts 02115, USA.
Ursula Hainz
Melinda A Biernacki
Wandi Zhang
Ann Cai
Jonathan S Duke-Cohan
Fenglong Liu
Vladimir Brusic
Donna Neuberg
Jeffery L Kutok
Edwin P Alyea
Christine M Canning
Robert J Soiffer
Jerome Ritz
Catherine J Wu
Harvard University · USBrigham and Women's Hospital · USDana-Farber Cancer Institute · USUniversity of Connecticut · USBeaumont Hospital, Royal Oak · US

Funding

Trageting the Multiple Myeloma EpigenomeP50CA100707 · NCI · DANA-FARBER CANCER INSTITUTE · PI ANDERSON, KENNETH C., MUNSHI, NIKHIL C. · 2003 to 2023
$45.0M
Targeting Genomic Instability and Evolution in MyelomaP01CA155258 · NCI · DANA-FARBER CANCER INST · PI Jill Corre · 2011 to 2026
$32.5M
Targeting Myeloma Cell-Host Bone Marrow InteractionsP01CA078378 · NCI · DANA-FARBER CANCER INSTITUTE · PI RITZ, JEROME · 1998 to 2014
$26.2M
GM-CSF secreting tumor cell vaccines to enhance post-transplant anti-CLL immunityR21CA132232 · NCI · DANA-FARBER CANCER INST · PI WU, CATHERINE JU-YING · 2008 to 2009
$757k
GM-CSF - producing tumor cell line as a CML vaccineR21CA115043 · NCI · DANA-FARBER CANCER INSTITUTE · PI WU, CATHERINE JU-YING · 2005 to 2006
$654k
Howard Hughes Medical InstituteNCI NIH HHS 5R21CA115043-2NCI NIH HHS P01 CA078378NCI NIH HHS P01 CA155258NCI NIH HHS P50 CA100707NCI NIH HHS R21 CA115043NCI NIH HHS R21 CA132232
6 · The paper itself

Abstract

Patients with chronic lymphocytic leukemia (CLL) who relapse after allogeneic transplant may achieve durable remission following donor lymphocyte infusion (DLI), showing the potency of donor-derived immunity in eradicating tumors. We sought to elucidate the antigenic basis of the effective graft-versus-leukemia (GvL) responses associated with DLI for the treatment of CLL by analyzing the specificity of plasma antibody responses developing in two DLI-treated patients who achieved long-term remission without graft-versus-host disease. By probing high-density protein microarrays with patient plasma, we discovered 35 predominantly intracellular antigens that elicited high-titer antibody reactivity greater in post-DLI than in pre-DLI plasma. Three antigens-C6orf130, MDS032, and ZFYVE19-were identified by both patients. Along with additional candidate antigens DAPK3, SERBP1, and OGFOD1, these proteins showed higher transcript and protein expression in B cells and CLL cells compared with normal peripheral blood mononuclear cells. DAPK3 and the shared antigens do not represent minor histocompatibility antigens, as their sequences are identical in both donor and tumor. Although ZFYVE19, DAPK3, and OGFOD1 elicited minimal antibody reactivity in 12 normal subjects and 12 chemotherapy-treated CLL patients, 5 of 12 CLL patients with clinical GvL responses were serologically reactive to these antigens. Moreover, antibody reactivity against these antigens was temporally correlated with clinical disease regression. These B-cell antigens represent promising biomarkers of effective anti-CLL immunity.

Indexed as

Antigens, SurfaceBiomarkers, TumorB-LymphocytesBone Marrow TransplantationCell LineageFemaleHumansImmunity, InnateImmunodominant EpitopesLeukemia, Lymphocytic, Chronic, B-CellMaleMiddle AgedMutationPrognosisProtein Array AnalysisTreatment OutcomeAntigens, SurfaceBiomarkers, TumorImmunodominant Epitopes

Identifiers

PMID20124481
PMCPMC2852266
OpenAlexW2093488156

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.