Evidence map›Paper›PMID 20460482›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2010

Graft-versus-leukemia antigen CML66 elicits coordinated B-cell and T-cell immunity after donor lymphocyte infusion.

Wandi Zhang, Jaewon Choi, Wanyong Zeng, Shelby A Rogers, Edwin P Alyea, James G Rheinwald, Christine M Canning, Vladimir Brusic, Tetsuro Sasada, Ellis L Reinherz and 3 more

Open access · bronzeAbstract readCase Reports
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

30 citing papers in PubMed, 38 citations in OpenAlex.

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  14. Adoptive Transfer of Invariant NKT Cells as Immunotherapy for Advanced Melanoma: A Phase I Clinical Trial.Clinical cancer research : an official journal of the American Association for Cancer Research · 2017
    Article
  15. Immunological off-target effects of imatinib.Nature reviews. Clinical oncology · 2016
    Review
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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

13 authors at 3 institutions in 1 country.

Wandi ZhangCancer Vaccine Center and Department of Medical Oncology, Dana-Farber Cancer Institute, Brigham and Women's Hospital and Harvard Skin Disease Research Center, Harvard Medical School, Boston, Massachusetts 02115, USA.
Jaewon Choi
Wanyong Zeng
Shelby A Rogers
Edwin P Alyea
James G Rheinwald
Christine M Canning
Vladimir Brusic
Tetsuro Sasada
Ellis L Reinherz
Jerome Ritz
Robert J Soiffer
Catherine J Wu
Brigham and Women's Hospital · USHarvard University · USDana-Farber Cancer Institute · US

Funding

Virus discovery in cutaneous T cell lymphomaP30AR042689 · NIAMS · BRIGHAM AND WOMEN'S HOSPITAL · PI KUPPER, THOMAS S. · 1994 to 2010
$6.8M
Post-transplant vaccines to enhance graft-versus-leukemia responsesR01HL103532 · NHLBI · DANA-FARBER CANCER INST · PI WU, CATHERINE JU-YING · 2010 to 2013
$1.7M
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 R21 CA115043NCI NIH HHS R21 CA132232NHLBI NIH HHS R01 HL103532NIAMS NIH HHS P30 AR042689NIAMS NIH HHS P30 AR42689
6 · The paper itself

Abstract

purposeThe target antigens of graft-versus-leukemia that are tumor associated are incompletely characterized. EXPERIMENTAL

designWe examined responses developing against CML66, an immunogenic antigen preferentially expressed in myeloid progenitor cells identified from a patient with chronic myelogenous leukemia who attained long-lived remission following CD4+ donor lymphocyte infusion (DLI).

resultsFrom this patient, CML66-reactive CD8+ T-cell clones were detected against an endogenously presented HLA-B*4403-restricted epitope (HDVDALLW). Neither CML66-specific antibody nor T-cell responses were detectable in peripheral blood before DLI. However, by 1 month after DLI, CD8+ T cells were present in peripheral blood and at 10-fold higher frequency in marrow. Subsequently, plasma antibody to CML66 developed in association with disease remission. Donor-derived CML66-reactive T cells were detected at low levels in vivo in marrow before DLI by ELISpot and by a nested PCR-based assay to detect clonotypic T-cell receptor sequences but not in blood of the patient pre-DLI nor of the graft donor.

conclusionsCD4+ DLI results in rapid expansion of preexisting marrow-resident leukemia-specific donor CD8+ T cells, followed by a cascade of antigen-specific immune responses detectable in blood. Our single-antigen analysis thus shows that durable posttransplant tumor immunity is directed in part against nonpolymorphic overexpressed leukemia antigens that elicit coordinated cellular and humoral immunity.

Indexed as

Lymphocyte TransfusionAntigen PresentationAntigens, NeoplasmB-LymphocytesCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesEpitopes, T-LymphocyteHLA AntigensHumansLeukemia, Myelogenous, Chronic, BCR-ABL PositiveLymphocyte ActivationNeoplasm Recurrence, LocalPolymerase Chain ReactionT-LymphocytesAntigens, NeoplasmEpitopes, T-LymphocyteHLA AntigensNUDCD1 protein, human

Identifiers

PMID20460482
PMCPMC2872105
OpenAlexW1972644764

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Registered trials

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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.