Evidence map›Paper›PMID 23403007›Full record

ArticleExperimental hematology2013

Enhancing cytokine-induced killer cell therapy of multiple myeloma.

Chunsheng Liu, Lukkana Suksanpaisan, Yun-Wen Chen, Stephen J Russell, Kah-Whye Peng

Open access · greenAbstract read
In one paragraph

Article in Experimental hematology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

14 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
  2. Article
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  4. Review
  5. Review
  6. Review
  7. Review
  8. Oncolytic Virotherapy: A Contest between Apples and Oranges.Molecular therapy : the journal of the American Society of Gene Therapy · 2017
    Review
  9. Review
  10. Article
  11. Review
  12. A killer choice for cancer immunotherapy.Immunologic research · 2014
    Review
  13. Article
  14. Review
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

5 authors at 1 institution in 1 country.

Chunsheng LiuDepartment of Molecular Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Lukkana Suksanpaisan
Yun-Wen Chen
Stephen J Russell
Kah-Whye Peng
Mayo Clinic · US

Funding

Use of microfluidic tumor cultures to enable clinical trials of therapies for ovarian cancerP50CA136393 · NCI · MAYO CLINIC ROCHESTER · PI Zhenkun Lou · 2009 to 2026
$37.0M
Antibody Neutralization of Therapeutic VirusesR01CA129966 · NCI · MAYO CLINIC ROCHESTER · PI RUSSELL, STEPHEN J · 2008 to 2012
$2.5M
Optimizing Measles Virotherapy in the Treatment of Ovarian CancerR01CA136547 · NCI · MAYO CLINIC ROCHESTER · PI GALANIS, EVANTHIA, PENG, KAH-WHYE · 2009 to 2012
$2.0M
Enhancing localization of therapeutic viruses and cells to tumor sitesR01CA129193 · NCI · MAYO CLINIC ROCHESTER · PI PENG, KAH-WHYE · 2009 to 2014
$1.8M
NCI NIH HHS CA129193NCI NIH HHS CA129966NCI NIH HHS CA136547NCI NIH HHS P50 CA136393NCI NIH HHS P50CA136393NCI NIH HHS R01 CA129193NCI NIH HHS R01 CA129966NCI NIH HHS R01 CA136547
6 · The paper itself

Abstract

Cytokine-induced killer (CIK) cells are in clinical testing against various tumor types, including multiple myeloma. In this study, we show that CIK cells have activity against subcutaneous and disseminated models of human myeloma (KAS-6/1), which can be enhanced by infecting the CIK cells with an oncolytic measles virus (MV) or by pretreating the myeloma cells with ionizing radiation (XRT). KAS-6/1 cells were killed by coculture with CIK or MV-infected CIK (CIK/MV) cells, and the addition of an anti-NKG2D antibody inhibited cytolysis by 50%. However, human bone marrow stromal cells can reduce CIK and CIK/MV mediated killing of myeloma cells (RPMI 8226, JJN-3 and MM1). In vivo, CIK and CIK/MV prolonged the survival of mice with systemic myeloma, although CIK/MV showed enhanced antitumor activity compared with CIK. Irradiation of the KAS-6/1 cells induced mRNA and protein expression of NKG2D ligands, MICA, and MICB in a dose-dependent manner and enhanced delivery of CIK/MV to the irradiated tumors. In both subcutaneous and disseminated myeloma models, XRT at 2 Gy resulted in superior prolongation of the survival of mice given CIK/MV therapy compared with CIK/MV with no XRT. This study demonstrates the potential of CIK against myeloma and that the combination of virotherapy with radiation could be used to further enhance therapeutic outcome using CIK cells.

Indexed as

Immunotherapy, AdoptiveOncolytic VirotherapyAnimalsAntibodies, MonoclonalAntigens, NeoplasmCells, CulturedCoculture TechniquesCombined Modality TherapyCytokine-Induced Killer CellsCytotoxicity, ImmunologicFemaleHistocompatibility Antigens Class IHumansMeasles virusMiceMice, Inbred ICRAntibodies, MonoclonalAntigens, NeoplasmHistocompatibility Antigens Class IKLRK1 protein, humanMHC class I-related chain AMICB antigenNK Cell Lectin-Like Receptor Subfamily KRNA, Messenger

Identifiers

PMID23403007
PMCPMC3669253
OpenAlexW1971787243

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.