Evidence map›Paper›PMID 25714118›Full record

Trial reportHuman vaccines & immunotherapeutics2015

Immunogenicity of GX301 cancer vaccine: Four (telomerase peptides) are better than one.

Daniela Fenoglio, Alessia Parodi, Rosa Lavieri, Francesca Kalli, Francesca Ferrera, Augusto Tagliamacco, Andrea Guastalla, Maria Giuseppina Lamperti, Mauro Giacomini, Gilberto Filaci

Registry-linked trialOpen access · hybridAbstract readClinical Trial
In one paragraph

Trial report in Human vaccines & immunotherapeutics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02293707 (A Randomised, Parallel-group, Open-label Phase II Trial of the Immunological Effects of Three Regimens of GX301 Vaccination in Castration-resistant Prostate Cancer Patients Who Have Achieved Response or Disease Stability With First-line Chemotherapy), which is not on this map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.1field-weighted citation impact, top 24% 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.

NCT02293707 phase2completednot on this map

A Randomised, Parallel-group, Open-label Phase II Trial of the Immunological Effects of Three Regimens of GX301 Vaccination in Castration-resistant Prostate Cancer Patients Who Have Achieved Response or Disease Stability With First-line Chemotherapy

TypeinterventionalSponsorLaboratoires Leurquin MediolanumRan2014 to 2019Enrolled99ConditionsProstate CancerArmsGX301
3 · Its place in the literature

Who cites it

23 citing papers in PubMed, 33 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. Review
  5. Review
  6. Review
  7. Review
  8. Telomeres and Cancer.Life (Basel, Switzerland) · 2021
    Review
  9. Review
  10. Review
  11. Review
  12. Review
  13. Review
  14. Article
  15. Review
  16. TERT-Regulation and Roles in Cancer Formation.Frontiers in immunology · 2020
    Review
  17. Article
  18. Telomerase-Targeted Cancer Immunotherapy.International journal of molecular sciences · 2019
    Review
  19. MYCN-targeting vaccines and immunotherapeutics.Human vaccines & immunotherapeutics · 2016
    Article
  20. 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

10 authors at 4 institutions in 2 countries.

Daniela Fenoglioa Centre of Excellence for Biomedical Research ; University of Genoa ; Genoa , Italy.
Alessia Parodi
Rosa Lavieri
Francesca Kalli
Francesca Ferrera
Augusto Tagliamacco
Andrea Guastalla
Maria Giuseppina Lamperti
Mauro Giacomini
Gilberto Filaci
University of Genoa · ITBioengineering (Switzerland) · CHIstituti di Ricovero e Cura a Carattere Scientifico · ITMediolanum Farmaceutici (Italy) · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Peptide540-548, peptide611-626, peptide672-686 and peptide766-780, which are derived from human telomerase, constitute the immunogenic component of the GX301 cancer vaccine. The relative immunogenicity of these peptides is unknown, thus it is unsure whether their combined use offers real advantages over single peptide stimulation. Hence, this study compared the number of specific immune responses and responders to each peptide, as well as to their mixture (meaning the co-presence of the 4 peptides in the same culture well), achieved after ex vivo stimulation of PBMC from 21, HLA-A2+ (n.11) or HLA-A2- (n.10), healthy donors. The study was performed on freshly collected PBMC (T0) and on PBMC stimulated for 10 d with single peptides or their mixture (T1). Peptide-specific immune responses were analyzed by Elispot and cytokine intracellular staining by flow cytometry. The results showed that each peptide induced specific immune responses in some subjects, with different panels of responders among the peptides. Moreover, the numbers of responses and responders to the single peptides or their mixture were comparable. Importantly, the overall number of responders to the 4 peptides was higher than to each single peptide, or to their mixture, both at T0 and T1. These data demonstrate the immunogenicity of each of the 4 GX301 telomerase peptides. Moreover, they show the advantage of multi-peptide over single peptide stimulation, providing a clear support to their combined administration in vaccination protocols. However, the data pose a warning against peptide administration as a mixture due to possible interference phenomena during antigen presentation processes.

Indexed as

AdultCancer VaccinesCell Line, TumorFemaleGenes, MHC Class IHLA-A2 AntigenHumansMaleMiddle AgedPeptidesTelomeraseCancer VaccinesHLA-A2 AntigenPeptidesTelomerasecancer vaccinesCIS, cytokine intracellular stainingCTL, cytotoxic T lymphocytescytokine intracellular stainingelispotFITC, fluorescein isothiocynateGX301IFNγ, interferon-gammaimmunogenicitymAb, monoclonal antibodyPBMC, peripheral blood mononuclear cellsPBS, phosphate buffered salinetelomerase

Identifiers

PMID25714118
PMCPMC4514186
OpenAlexW1485620077

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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.