Evidence map›Paper›PMID 19118005›Full record

ArticleCancer research2009

Genetic regulation of the response to Her-2 DNA vaccination in human Her-2 transgenic mice.

Olga Radkevich-Brown, Jennifer Jacob, Michael Kershaw, Wei-Zen Wei

Open access · bronzeAbstract read
In one paragraph

Article in Cancer research, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Camouflage and sabotage: tumor escape from the immune system.Cancer immunology, immunotherapy : CII · 2011
    Review
  14. Article
  15. Anti-HER2 vaccines: new prospects for breast cancer therapy.Cancer immunology, immunotherapy : CII · 2010
    Review
  16. Article
  17. Article
  18. 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

4 authors at 3 institutions in 2 countries.

Olga Radkevich-BrownKarmanos Cancer Institute, Wayne State University, 110 E. Warren Avenue, Detroit, MI 48201, USA.
Jennifer Jacob
Michael Kershaw
Wei-Zen Wei
Wayne State University · USPeter MacCallum Cancer Centre · AUThe Barbara Ann Karmanos Cancer Institute · US

Funding

DEVELOPMENT OF ERBB2 BASED BREAST CANCER VACCINESR01CA076340 · NCI · WAYNE STATE UNIVERSITY · PI WEI, WEI-ZEN · 1998 to 2020
$5.2M
Tilting the balance in cancer immunotherapy and autoimmunityR01CA125680 · NCI · WAYNE STATE UNIVERSITY · PI WEI, WEI-ZEN · 2006 to 2010
$1.3M
NCI NIH HHS CA 125680NCI NIH HHS CA 76340NCI NIH HHS R01 CA076340NCI NIH HHS R01 CA125680
6 · The paper itself

Abstract

Genetic regulation of immune reactivity to Her-2 vaccination and the consequent antitumor effect was tested in human Her-2 transgenic (Tg) mice of C57BL/6 (B6), BALB/c (BALB), and (B6x BALB) F1 (F1) background. Mice were electrovaccinated with Her-2 DNA with or without pretreatment with CD25 monoclonal antibody to remove CD25(hi) regulatory T cells. When CD25(+) T cells were intact, BALB Her-2 Tg mice were more responsive than the other two strains in both humoral and cellular immunities, and their tumor growth was significantly delayed. B6 Her-2 Tg mice responded poorly and F1 mice showed modest immune reactivity, but tumor growth did not change in either strain. Depletion of CD25(hi) T cells before vaccination significantly improved protection from tumor challenge in F1 Her-2 Tg mice. This was associated with elevated levels of Her-2 IgG1, IgG2a, and IgG2c antibodies, and some mice also showed IFN-gamma producing T-cell response. The same treatment induced modest improvement in B6 Her-2 Tg mice. In BALB Her-2 Tg mice, however, depletion of CD25(hi) T cells did not further improve antitumor efficacy. Although their Her-2-specific IgG1 and interleukin-5-secreting T cells increased, the levels of IgG2a and IFN-gamma-secreting T cells did not change. These results are the first to show genetic regulation of the response to a cancer vaccine and an unequal effect of removing CD25(hi) T cells on antitumor immunity. These results warrant individualized treatment plans for patients with heterogeneous genetic backgrounds and possibly differential intrinsic immune reactivity to tumor antigens.

Indexed as

AnimalsAntibodies, MonoclonalCancer VaccinesCell Line, TumorErb-b2 Receptor Tyrosine KinasesFemaleHumansInterleukin-2 Receptor alpha SubunitLymphocyte ActivationMammary Neoplasms, AnimalMiceMice, Inbred BALB CMice, Inbred C57BLMice, TransgenicT-LymphocytesT-Lymphocytes, RegulatoryAntibodies, MonoclonalCancer VaccinesErb-b2 Receptor Tyrosine KinasesInterleukin-2 Receptor alpha SubunitVaccines, DNA

Identifiers

PMID19118005
PMCPMC2613542
OpenAlexW2053358282

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.