Evidence map›Paper›PMID 19225534›Full record

ArticleLeukemia2009

Cyclin D1 as a universally expressed mantle cell lymphoma-associated tumor antigen for immunotherapy.

M Wang, L Sun, J Qian, X Han, L Zhang, P Lin, Z Cai, Q Yi

Abstract read
In one paragraph

Article in Leukemia, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

20 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Colorectal cancer prevention: Immune modulation taking the stage.Biochimica et biophysica acta. Reviews on cancer · 2018
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Cyclin D as a therapeutic target in cancer.Nature reviews. Cancer · 2011
    Review
  17. Cell cyclins: triggering elements of cancer or not?World journal of surgical oncology · 2010
    Review
  18. Article
  19. Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

M WangDivision of Cancer Medicine, Department of Lymphoma and Myeloma, University of Texas M.D. Anderson Cancer Center, Houston, TX 77030, USA.
L Sun
J Qian
X Han
L Zhang
P Lin
Z Cai
Q Yi
The University of Texas MD Anderson Cancer Center · US

Funding

Idiotype-specific effector T cells in multiple myelomaR01CA096569 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI YI, QING · 2002 to 2006
$1.5M
Optimizing Dendritic Cell Immunotherapy in MyelomaR01CA103978 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI YI, QING · 2004 to 2008
$1.4M
NCI NIH HHS R01 CA096569NCI NIH HHS R01 CA103978NCI NIH HHS R01 CA96569
6 · The paper itself

Abstract

Mantle cell lymphoma (MCL) accounts for 5-10% of all non-Hodgkin lymphomas and has the worst prognosis among all lymphomas. The hallmark of MCL is a t(11;14) translocation that results in overexpression of cyclin D1 by tumor cells of virtually all patients. In this study, we examined whether cyclin D1 could be an effective tumor-associated antigen for immunotherapy. We identified cyclin D1 peptides for HLA-A(*)0201 and generated peptide-specific CD8(+) T-cell lines from HLA-A(*)0201(+) blood donors and MCL patients. These cell lines proliferated in response to cyclin D1 peptide-pulsed stimulatory cells. Moreover, the T cells efficiently lysed peptide-pulsed but not unpulsed T2 cells and autologous dendritic cells; cyclin D1(+) and HLA-A(*)0201(+) human MCL lines MINO, SP53, Jeko-1 and Granta 519; and more importantly, HLA-A(*)0201(+) primary lymphoma cells from MCL patients. No killing was observed with HLA-A(*)0201(-) primary lymphoma cells or HLA-A(*)0201(+) normal blood cells, including B cells. These results indicate that these T cells are potent cytotoxic T cells and recognize cyclin D1 peptides naturally presented by patient lymphoma cells in the context of HLA-A(*)0201 molecules. Taken together, our work identifies cyclin D1 as a potentially important antigen for immunotherapy of MCL.

Indexed as

ImmunotherapyBlotting, WesternB-LymphocytesCell Line, TumorCell ProliferationCyclin D1Cytotoxicity, ImmunologicHumansImmunohistochemistryImmunophenotypingInterferon-gammaLymphoma, Mantle-CellMajor Histocompatibility ComplexT-LymphocytesCyclin D1Interferon-gamma

Identifiers

PMID19225534
PMCPMC5890427
OpenAlexW2025086370

What OpenQuestion holds

Textmetadata
LicenceTDM
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.