Evidence map›Paper›PMID 27377043›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2016

Enhancing Antitumor Immune Responses by Optimized Combinations of Cell-penetrating Peptide-based Vaccines and Adjuvants.

Elodie Belnoue, Wilma Di Berardino-Besson, Hubert Gaertner, Susanna Carboni, Isabelle Dunand-Sauthier, Fabrice Cerini, Else-Marit Suso-Inderberg, Sébastien Wälchli, Stéphane König, Andres M Salazar and 4 more

Open access · hybridAbstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed, 40 citations in OpenAlex.

  1. Review
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  4. Cancer-Targeting Applications of Cell-Penetrating Peptides.International journal of molecular sciences · 2024
    Review
  5. Article
  6. Article
  7. Review
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  9. Cell-penetrating peptides enhance peptide vaccine accumulation and persistence in lymph nodes to drive immunogenicity.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
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  12. Review
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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

14 authors at 4 institutions in 3 countries.

Elodie BelnoueAmal Therapeutics, Geneva, Switzerland.
Wilma Di Berardino-BessonCenter of Oncology, Geneva University Hospitals and University of Geneva, Geneva, Switzerland.
Hubert GaertnerDepartment of Pathology and Immunology, University of Geneva, Geneva, Switzerland.
Susanna CarboniAmal Therapeutics, Geneva, Switzerland.
Isabelle Dunand-SauthierDepartment of Pathology and Immunology, University of Geneva, Geneva, Switzerland.
Fabrice CeriniDepartment of Pathology and Immunology, University of Geneva, Geneva, Switzerland.
Else-Marit Suso-InderbergDepartment of Cellular Therapy, Oslo University Hospital Radiumhospitalet, Oslo, Norway.
Sébastien WälchliDepartment of Cellular Therapy, Oslo University Hospital Radiumhospitalet, Oslo, Norway.
Stéphane KönigDepartment of Basic Neurosciences, University of Geneva, Geneva, Switzerland.
Andres M SalazarOncovir, Washington DC, USA.
Oliver HartleyDepartment of Pathology and Immunology, University of Geneva, Geneva, Switzerland.
Pierre-Yves DietrichCenter of Oncology, Geneva University Hospitals and University of Geneva, Geneva, Switzerland.
Paul R WalkerCenter of Oncology, Geneva University Hospitals and University of Geneva, Geneva, Switzerland.
Madiha DerouaziAmal Therapeutics, Geneva, Switzerland.
University of Geneva · CHOslo University Hospital · NOOncovir (United States) · USUniversity Hospital of Geneva · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cell penetrating peptides (CPPs) from the protein ZEBRA are promising candidates to exploit in therapeutic cancer vaccines, since they can transport antigenic cargos into dendritic cells and induce tumor-specific T cells. Employing CPPs for a given cancer indication will require engineering to include relevant tumor-associated epitopes, administration with an appropriate adjuvant, and testing for antitumor immunity. We assessed the importance of structural characteristics, efficiency of in vitro transduction of target cells, and choice of adjuvant in inducing the two key elements in antitumor immunity, CD4 and CD8 T cells, as well as control of tumor growth in vivo. Structural characteristics associated with CPP function varied according to CPP truncations and cargo epitope composition, and correlated with in vitro transduction efficiency. However, subsequent in vivo capacity to induce CD4 and CD8 T cells was not always predicted by in vitro results. We determined that the critical parameter for in vivo efficacy using aggressive mouse tumor models was the choice of adjuvant. Optimal pairing of a particular ZEBRA-CPP sequence and antigenic cargo together with adjuvant induced potent antitumor immunity. Our results highlight the irreplaceable role of in vivo testing of novel vaccine constructs together with adjuvants to select combinations for further development.

Indexed as

Adjuvants, ImmunologicAnimalsCancer VaccinesCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCell Line, TumorCell-Penetrating PeptidesCircular DichroismCross-PrimingDendritic CellsDisease Models, AnimalEpitopes, T-LymphocyteFemaleHistocompatibility Antigens Class IHistocompatibility Antigens Class IIHumansAdjuvants, ImmunologicBZLF1 protein, Herpesvirus 4, HumanCancer VaccinesCell-Penetrating PeptidesEpitopes, T-LymphocyteHistocompatibility Antigens Class IHistocompatibility Antigens Class IITrans-Activators

Identifiers

PMID27377043
PMCPMC5113103
OpenAlexW2471219242

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.