Evidence map›Paper›PMID 20234340›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2010

Systemic therapy of disseminated myeloma in passively immunized mice using measles virus-infected cell carriers.

Chunsheng Liu, Stephen J Russell, Kah-Whye Peng

Open access · hybridAbstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
7.2field-weighted citation impact, top 3% 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

51 citing papers in PubMed, 69 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. Syncytia Formation in Oncolytic Virotherapy.Molecular therapy oncolytics · 2019
    Review
  10. Review
  11. Article
  12. Review
  13. Review
  14. Potential and clinical translation of oncolytic measles viruses.Expert opinion on biological therapy · 2017
    Review
  15. Oncolytic Viral Therapy for Mesothelioma.Frontiers in oncology · 2017
    Review
  16. Review
  17. Review
  18. Article
  19. Article
  20. Article
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

3 authors at 1 institution in 1 country.

Chunsheng LiuDepartment of Molecular Medicine, Mayo Clinic, Rochester, Minnesota 55905, USA.
Stephen J Russell
Kah-Whye Peng
Mayo Clinic · US

Funding

Radiovirotherapy for Multiple MyelomaR01CA100634 · NCI · MAYO CLINIC ROCHESTER · PI RUSSELL, STEPHEN J · 2003 to 2012
$3.2M
Antibody Neutralization of Therapeutic VirusesR01CA129966 · NCI · MAYO CLINIC ROCHESTER · PI RUSSELL, STEPHEN J · 2008 to 2012
$2.5M
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 CA100634NCI NIH HHS CA129193NCI NIH HHS CA129966NCI NIH HHS R01 CA100634NCI NIH HHS R01 CA129193NCI NIH HHS R01 CA129966
6 · The paper itself

Abstract

Multiple myeloma (MM) is bone marrow plasma cell malignancy. A clinical trial utilizing intravenous administration of oncolytic measles virus (MV) encoding the human sodium-iodide symporter (MV-NIS) is ongoing in myeloma patients. However, intravenously administered MV-NIS is rapidly neutralized by antiviral antibodies. Because myeloma cell lines retain bone marrow tropism, they may be ideal as carriers for delivery of MV-NIS to myeloma deposits. A disseminated human myeloma (KAS 6/1) model was established. Biodistribution of MM1, a myeloma cell line, was determined after intravenous infusion. MM1 cells were found in the spine, femurs, and mandibles of tumor-bearing mice. Lethally irradiated MM1 cells remained susceptible to measles infection and transferred MV to KAS 6/1 cells in the presence of measles immune sera. Mice-bearing disseminated myeloma and passively immunized with measles immune serum were given MV-NIS or lethally irradiated MV-NIS-infected MM1 carriers. The antitumor activity of MV-NIS was evident only in measles naive mice and not in passively immunized mice. In contrast, survivals of both measles naive and immune mice were extended using MV-NIS-infected MM1 cell carriers. Hence, we demonstrate for the first time that systemically administered cells can serve as MV carriers and prolonged survival of mice with pre-existing antimeasles antibodies.

Indexed as

Immunization, PassiveMeasles virusOncolytic VirotherapyAnimalsAntibodies, NeutralizingChlorocebus aethiopsHumansImmune SeraMiceMice, SCIDMultiple MyelomaVero CellsAntibodies, NeutralizingImmune Sera

Identifiers

PMID20234340
PMCPMC2889728
OpenAlexW2067885236

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.