Evidence map›Paper›PMID 26587315›Full record

ArticleOncoimmunology2015

Can dendritic cells improve whole cancer cell vaccines based on immunogenically killed cancer cells?

Laetitia Cicchelero, Sofie Denies, Bert Devriendt, Hilde de Rooster, Niek N Sanders

Open access · goldAbstract read
In one paragraph

Article in Oncoimmunology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. 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

5 authors at 3 institutions in 3 countries.

Laetitia CiccheleroLaboratory of Gene Therapy, Department of Nutrition, Genetics and Ethology; Faculty of Veterinary Medicine; Ghent University ; Merelbeke, Belgium.
Sofie DeniesLaboratory of Gene Therapy, Department of Nutrition, Genetics and Ethology; Faculty of Veterinary Medicine; Ghent University ; Merelbeke, Belgium.
Bert DevriendtLaboratory of Immunology, Department of Virology, Parasitology and Immunology; Faculty of Veterinary Medicine; Ghent University , Merelbeke, Belgium.
Hilde de RoosterSmall Animal Hospital, Department of Medicine and Clinical Biology of Small Animals; Faculty of Veterinary Medicine; Ghent University , Merelbeke, Belgium.
Niek N SandersLaboratory of Gene Therapy, Department of Nutrition, Genetics and Ethology; Faculty of Veterinary Medicine; Ghent University ; Merelbeke, Belgium.
University of Veterinary Medicine · HUGhent University · BEGhent University Hospital · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immunogenic cell death (ICD) offers interesting opportunities in cancer cell (CC) vaccine manufacture, as it increases the immunogenicity of the dead CC. Furthermore, fusion of CCs with dendritic cells (DCs) is considered a superior method for generating whole CC vaccines. Therefore, in this work, we determined in naive mice whether immunogenically killed CCs per se (CC vaccine) elicit an antitumoral immune response different from the response observed when immunogenically killed CCs are associated with DCs through fusion (fusion vaccine) or through co-incubation (co-incubation vaccine). After tumor inoculation, the type of immune response in the prophylactically vaccinated mice differed between the groups. In more detail, fusion vaccines elicited a humoral anticancer response, whereas the co-incubation and CC vaccine mainly induced a cellular response. Despite these differences, all three approaches offered a prophylactic protection against tumor development in the murine mammary carcinoma model. In summary, it can be concluded that whole CC vaccines based on immunogenically killed CCs may not necessarily require association with DCs to elicit a protective anticancer immune response. If this finding can be endorsed in other cancer models, the manufacture of CC vaccines would greatly benefit from this new insight, as production of DC-based vaccines is laborious, time-consuming and expensive.

Indexed as

co-incubationfusionimmunogenic cell deathwhole cancer cell vaccine

Identifiers

PMID26587315
PMCPMC4635695
OpenAlexW2171731873

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.