Evidence map›Paper›PMID 17597331›Full record

ArticleCancer immunology, immunotherapy : CII2007

Induction of protective immune responses against NXS2 neuroblastoma challenge in mice by immunotherapy with GD2 mimotope vaccine and IL-15 and IL-21 gene delivery.

Aleksandra Kowalczyk, Andrzej Wierzbicki, Margaret Gil, Barbara Bambach, Yutaro Kaneko, Hanna Rokita, Elizabeth Repasky, Robert Fenstermaker, Martin Brecher, Michael Ciesielski and 1 more

Open access · greenAbstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

17 citing papers in PubMed, 32 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Impact of minimal tumor burden on antibody response to vaccination.Cancer immunology, immunotherapy : CII · 2011
    Article
  11. Treatment of high-risk neuroblastoma with anti-GD2 antibodies.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2010
    Review
  12. Review
  13. Review
  14. Article
  15. RESEARCH ADVANCES IN NEUROBLASTOMA IMMUNOTHERAPY.Current pediatric reviews · 2009
    Article
  16. Article
  17. 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

11 authors at 3 institutions in 3 countries.

Aleksandra KowalczykDepartment of Immunology, Roswell Park Cancer Institute, Elm and Carlton Streets, Buffalo, NY 14263, USA. danuta.kozbor@roswellpark.org
Andrzej Wierzbicki
Margaret Gil
Barbara Bambach
Yutaro Kaneko
Hanna Rokita
Elizabeth Repasky
Robert Fenstermaker
Martin Brecher
Michael Ciesielski
Danuta Kozbor
Roswell Park Comprehensive Cancer Center · USJagiellonian University · PLKindai University · JP

Funding

Impact of IL-21 on HIV VaccineR21AI060375 · NIAID · ROSWELL PARK CANCER INSTITUTE CORP · PI KOZBOR, DANUTA B · 2005 to 2006
$511k
NIAID NIH HHS R21 AI060375
6 · The paper itself

Abstract

The GD2 ganglioside expressed on neuroectodermal tumor cells is weakly immunogenic in tumor-bearing patients and induces predominantly IgM antibody responses in the immunized host. Using a syngeneic mouse challenge model with GD2-expressing NXS2 neuroblastoma, we investigated novel strategies for augmenting the effector function of GD2-specific antibody responses induced by a mimotope vaccine. We demonstrated that immunization of A/J mice with DNA vaccine expressing the 47-LDA mimotope of GD2 in combination with IL-15 and IL-21 genes enhanced the induction of GD2 cross-reactive IgG2 antibody responses that exhibited cytolytic activity against NXS2 cells. The combined immunization regimen delivered 1 day after tumor challenge inhibited subcutaneous (s.c.) growth of NXS2 neuroblastoma in A/J mice. The vaccine efficacy was reduced after depletion of NK cells as well as CD4(+) and CD8(+) T lymphocytes suggesting involvement of innate and adaptive immune responses in mediating the antitumor activity in vivo. CD8(+) T cells isolated from the immunized and cured mice were cytotoxic against syngeneic neuroblastoma cells but not against allogeneic EL4 lymphoma, and exhibited antitumor activity after adoptive transfer in NXS2-challenged mice. We also demonstrated that coimmunization of NXS2-challenged mice with the IL-15 and IL-21 gene combination resulted in enhanced CD8(+) T cell function that was partially independent of CD4(+) T cell help in inhibiting tumor growth. This study is the first demonstration that the mimotope vaccine of a weakly immunogenic carbohydrate antigen in combination with plasmid-derived IL-15 and IL-21 cytokines induces both innate and adaptive arms of the immune system leading to the generation of effective protection against neuroblastoma challenge.

Indexed as

GangliosidesAnimalsCancer VaccinesCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCell LineDendritic CellsFemaleGenetic VectorsImmunotherapy, AdoptiveInterferon-gammaInterleukin-15Interleukin-21InterleukinsMiceNeuroblastomaCancer Vaccinesganglioside, GD2GangliosidesInterferon-gammaInterleukin-15Interleukin-21Interleukins

Identifiers

PMID17597331
PMCPMC11030615
OpenAlexW2081036165

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.