Evidence map›Paper›PMID 27056671›Full record

ArticleCancer gene therapy2016

CCL4 as an adjuvant for DNA vaccination in a Her2/neu mouse tumor model.

T Nguyen-Hoai, M Pham-Duc, M Gries, B Dörken, A Pezzutto, J Westermann

Abstract read
PubMed Publisher
In one paragraph

Article in Cancer gene therapy, 2016. 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
1.4field-weighted citation impact, top 20% 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, 22 citations in OpenAlex.

  1. Article
  2. Article
  3. [Research Progresses on the Effects of CCL4 on Immune Escape 
in Tumor Microenvironment].Zhongguo fei ai za zhi = Chinese journal of lung cancer · 2024
    Review
  4. The future of cancer immunotherapy: DNA vaccines leading the way.Medical oncology (Northwood, London, England) · 2023
    Review
  5. Review
  6. Article
  7. Review
  8. Engineering Targeting Materials for Therapeutic Cancer Vaccines.Frontiers in bioengineering and biotechnology · 2020
    Review
  9. Article
  10. Cancer DNA vaccines: current preclinical and clinical developments and future perspectives.Journal of experimental & clinical cancer research : CR · 2019
    Review
  11. Article
  12. Article
  13. Clinical applications of mouse models for breast cancer engaging HER2/neu.Integrative cancer science and therapeutics · 2016
    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

6 authors at 2 institutions in 1 country.

T Nguyen-HoaiDepartment of Hematology, Oncology, and Tumor Immunology, Charit-University Medicine Berlin, Campus Virchow, Berlin, Germany.
M Pham-DucDepartment of Hematology, Oncology, and Tumor Immunology, Charit-University Medicine Berlin, Campus Virchow, Berlin, Germany.
M GriesDepartment of Hematology, Oncology, and Tumor Immunology, Charit-University Medicine Berlin, Campus Virchow, Berlin, Germany.
B DörkenDepartment of Hematology, Oncology, and Tumor Immunology, Charit-University Medicine Berlin, Campus Virchow, Berlin, Germany.
A PezzuttoDepartment of Hematology, Oncology, and Tumor Immunology, Charit-University Medicine Berlin, Campus Virchow, Berlin, Germany.
J WestermannDepartment of Hematology, Oncology, and Tumor Immunology, Charit-University Medicine Berlin, Campus Virchow, Berlin, Germany.
Max Delbrück Center · DECharité - Universitätsmedizin Berlin · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chemokines are key regulators of both innate and adaptive immune responses. CCL4 (macrophage inflammatory protein-1β, MIP-1β) is a CC chemokine that has a broad spectrum of target cells including immature dendritic cells, which express the cognate receptor CCR5. We asked whether a plasmid encoding CCL4 is able to improve tumor protection and immune responses in a Her2/neu+ mouse tumor model. Balb/c mice were immunized twice intramuscularly with plasmid DNA on days 1 and 15. On day 25, a tumor challenge was performed with 2 × 10(5) syngeneic Her2/neu+ D2F2/E2 tumor cells. Different groups of mice were vaccinated with pDNA(Her2/neu) plus pDNA(CCL4), pDNA(Her2/neu), pDNA(CCL4) or mock vector alone. Our results show that CCL4 is able to (i) improve tumor protection and (ii) augment a TH1-polarized immune response against Her2/neu. Although Her2/neu-specific humoral and T-cell immune responses were comparable with that induced in previous studies using CCL19 or CCL21 as adjuvants, tumor protection conferred by CCL4 was inferior. Whether this is due to a different spectrum of (innate) immune cells, remains to be clarified. However, combination of CCL19/21 with CCL4 might be a reasonable approach in the future, particularly for DNA vaccination in Her2/neu+ breast cancer in the situation of minimal residual disease.

Indexed as

Adjuvants, ImmunologicChemokine CCL4AnimalsCancer VaccinesCell LineDisease Models, AnimalErb-b2 Receptor Tyrosine KinasesFemaleGene ExpressionGene OrderHumansImmunizationMammary Neoplasms, ExperimentalMicePlasmidsTumor BurdenAdjuvants, ImmunologicCancer VaccinesChemokine CCL4Erb-b2 Receptor Tyrosine KinasesVaccines, DNA

Identifiers

PMID27056671
OpenAlexW2330259340

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.