Evidence map›Paper›PMID 23603859›Full record

ArticleJournal of immunotherapy (Hagerstown, Md. : 1997)2013

Long-lasting complete regression of established mouse tumors by counteracting Th2 inflammation.

Min Dai, Huafeng Wei, Yuen Yee Yip, Qinghua Feng, Kecheng He, Viorica Popov, Ingegerd Hellstrom, Karl Erik Hellstrom

Abstract read
In one paragraph

Article in Journal of immunotherapy (Hagerstown, Md. : 1997), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

28 citing papers in PubMed, 45 citations in OpenAlex.

  1. Article
  2. Review
  3. CD137Cancers · 2021
    Review
  4. Review
  5. Article
  6. Review
  7. An Update on Anti-CD137 Antibodies in Immunotherapies for Cancer.International journal of molecular sciences · 2019
    Review
  8. Review
  9. Article
  10. Tumor Regression and Cure Depends on Sustained Th1 Responses.Journal of immunotherapy (Hagerstown, Md. : 1997) · 2018
    Article
  11. Immune checkpoint inhibitors in cancer therapy.Journal of biomedical research · 2018
    Article
  12. Article
  13. Review
  14. Review
  15. Review
  16. Review
  17. IL2 Inducible T-cell Kinase, a Novel Therapeutic Target in Melanoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2015
    Article
  18. Immunomodulatory antibody therapy of cancer: the closer, the better.Clinical cancer research : an official journal of the American Association for Cancer Research · 2015
    Article
  19. Curing mice with large tumors by locally delivering combinations of immunomodulatory antibodies.Clinical cancer research : an official journal of the American Association for Cancer Research · 2015
    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

8 authors at 3 institutions in 2 countries.

Min DaiDepartment of Pathology, Harborview Medical Center, University of Washington, Seattle, WA 98104-2499, USA.
Huafeng Wei
Yuen Yee Yip
Qinghua Feng
Kecheng He
Viorica Popov
Ingegerd Hellstrom
Karl Erik Hellstrom
Harborview Medical Center · USSecond Military Medical University · CNUniversity of Washington · US

Funding

Mesothelin as biomarker and therapeutic targetR01CA134487 · NCI · UNIVERSITY OF WASHINGTON · PI HELLSTROM, INGEGERD E · 2008 to 2011
$1.3M
Melanoma vaccinesR01CA112073 · NCI · UNIVERSITY OF WASHINGTON · PI HELLSTROM, KARL ERIK · 2005 to 2007
$701k
NCI NIH HHS R01 CA112073NCI NIH HHS R01 CA134487NCI NIH HHS R01CA134487PHS HHS R01-112073
6 · The paper itself

Abstract

Mice with intraperitoneal ID8 ovarian carcinoma or subcutaneous SW1 melanoma were injected with monoclonal antibodies (mAbs) to CD137PD-1CTLA4 7-15 days after tumor initiation. Survival of mice with ID8 tumors tripled and >40% of mice with SW1 tumors remained healthy >150 days after last treatment and are probably cured. Therapeutic efficacy was associated with a systemic immune response with memory and antigen specificity, required CD4 cells and involved CD8 cells and NK cells to a less extent. The 3 mAb combination significantly decreased CD19 cells at tumor sites, increased IFN-γ and TNF-α producing CD4 and CD8 T cells and mature CD86 dendritic cells (DC), and it increased the ratios of effector CD4 and CD8 T cells to CD4Foxp3 regulatory T (Treg) cells and to CD11bGr-1 myeloid suppressor cells (MDSC). This is consistent with shifting the tumor microenvironment from an immunosuppressive Th2 to an immunostimulatory Th1 type and is further supported by PCR data. Adding an anti-CD19 mAb to the 3 mAb combination in the SW1 model further increased therapeutic efficacy. Data from ongoing experiments show that intratumoral injection of a combination of mAbs to CD137PD-1CTLA4CD19 can induce complete regression and dramatically prolong survival also in the TC1 carcinoma and B16 melanoma models, suggesting that the approach has general validity.

Indexed as

AnimalsAntibodies, MonoclonalAntigens, CD19Antigens, DifferentiationCell Line, TumorCTLA-4 AntigenDisease Models, AnimalEpitopesFemaleGene Expression ProfilingImmunophenotypingInflammationLymphocyte DepletionMelanoma, ExperimentalMiceNeoplasmsAntibodies, MonoclonalAntigens, CD19Antigens, DifferentiationCTLA-4 AntigenEpitopesPdcd1 protein, mouseProgrammed Cell Death 1 ReceptorTumor Necrosis Factor Receptor Superfamily, Member 9

Identifiers

PMID23603859
PMCPMC3685275
OpenAlexW2329106076

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.