Evidence map›Paper›PMID 15696196›Full record

Trial reportThe Journal of clinical investigation2005

Rapid and strong human CD8+ T cell responses to vaccination with peptide, IFA, and CpG oligodeoxynucleotide 7909.

Daniel E Speiser, Danielle Liénard, Nathalie Rufer, Verena Rubio-Godoy, Donata Rimoldi, Ferdy Lejeune, Arthur M Krieg, Jean-Charles Cerottini, Pedro Romero

Registry-linked trialOpen access · bronzeAbstract readClinical TrialClinical Trial, Phase I
In one paragraph

Trial report in The Journal of clinical investigation, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00112229 (Immunotherapy of HLA-A2 Positive Stage III/IV Melanoma Patients With CpG7909, Tumor Antigenic Peptides and Montanide), which is not on this map. Cited by 236 papers.

0numbers the graph read from it
0cells of the map it votes in
236citing papers in PubMed
21.4field-weighted citation impact, top 1% 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.

NCT00112229 phase1completednot on this map

Immunotherapy of HLA-A2 Positive Stage III/IV Melanoma Patients With CpG7909, Tumor Antigenic Peptides and Montanide

TypeinterventionalSponsorCentre Hospitalier Universitaire VaudoisRan2003 to 2012Enrolled29ConditionsMelanomaArmsgroup 1, group 2, group 3, group 4
3 · Its place in the literature

Who cites it

236 citing papers in PubMed, 621 citations in OpenAlex.

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  16. Stimuli-responsive STING nanovaccine for systemic therapy of HPV-induced cancers.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  17. Review
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  20. Toll-like receptor agonists as cancer vaccine adjuvants.Human vaccines & immunotherapeutics · 2024
    Review

176 more citing papers are in PubMed but not listed here.

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

9 authors at 4 institutions in 3 countries.

Daniel E SpeiserDivision of Clinical Onco-Immunology, Ludwig Institute for Cancer Research, Multidisciplinary Oncology Center, Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland. daniel.speiser@hospvd.ch.
Danielle Liénard
Nathalie Rufer
Verena Rubio-Godoy
Donata Rimoldi
Ferdy Lejeune
Arthur M Krieg
Jean-Charles Cerottini
Pedro Romero
Ludwig Cancer Research · BELudwig Cancer Research · CHUniversity Hospital of Lausanne · CHWellesley College · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The induction of potent CD8+ T cell responses by vaccines to fight microbes or tumors remains a major challenge, as many candidates for human vaccines have proved to be poorly immunogenic. Deoxycytidyl-deoxyguanosin oligodeoxynucleotides (CpG ODNs) trigger Toll-like receptor 9, resulting in dendritic cell maturation that can enhance immunogenicity of peptide-based vaccines in mice. We tested whether a synthetic ODN, CpG 7909, could improve human tumor antigen-specific CD8+ T cell responses. Eight HLA-A2+ melanoma patients received 4 monthly vaccinations of low-dose CpG 7909 mixed with melanoma antigen A (Melan-A; identical to MART-1) analog peptide and incomplete Freund's adjuvant. All patients exhibited rapid and strong antigen-specific T cell responses: the frequency of Melan-A-specific T cells reached over 3% of circulating CD8+ T cells. This was one order of magnitude higher than the frequency seen in 8 control patients treated similarly but without CpG and 1-3 orders of magnitude higher than that seen in previous studies with synthetic vaccines. The enhanced T cell populations consisted primarily of effector memory cells, which in part secreted IFN- and expressed granzyme B and perforin ex vivo. In vitro, T cell clones recognized and killed melanoma cells in an antigen-specific manner. Thus, CpG 7909 is an efficient vaccine adjuvant that promotes strong antigen-specific CD8+ T cell responses in humans.

Indexed as

Lymphocyte ActivationVaccinationAnimalsAntigens, NeoplasmCancer VaccinesCD8-Positive T-LymphocytesFreund's AdjuvantHLA-A2 AntigenHumansInterferon-gammaLipidsMART-1 AntigenMelanomaNeoplasm ProteinsOligodeoxyribonucleotidesQuality ControlAntigens, NeoplasmCancer VaccinesFreund's AdjuvantHLA-A2 Antigenincomplete Freund's adjuvantInterferon-gammaLipidsMART-1 AntigenMLANA protein, humanMlana protein, mouseNeoplasm ProteinsOligodeoxyribonucleotidesProMune

Identifiers

PMID15696196
PMCPMC546459
OpenAlexW2095224835

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.