Evidence map›Paper›PMID 16034561›Full record

Trial reportCancer immunology, immunotherapy : CII2006

Induction of cellular immune responses against carcinoembryonic antigen in patients with metastatic tumors after vaccination with altered peptide ligand-loaded dendritic cells.

Jana Babatz, Christoph Röllig, Bärbel Löbel, Gunnar Folprecht, Michael Haack, Heinrich Günther, Claus-Henning Köhne, Gerhard Ehninger, Marc Schmitz, Martin Bornhäuser

5 registry-linked trialsOpen access · greenAbstract readClinical Trial, Phase IClinical Trial, Phase II
In one paragraph

Trial report in Cancer immunology, immunotherapy : CII, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 5 registered trials, which are not on this map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 16% 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.

NCT02632006 phase1 / phase2unknown statusnot on this mapstarted 2015, after this paper: background citation

A Clinical Study of Adoptive Cellular Immunotherapy Using Pluripotent Killer T Cells Expressing Antibodies for Programmed Death 1 (PD-1) in Treating Patients With Advanced Hepatocellular Carcinoma

TypeinterventionalSponsorSecond Military Medical UniversityRan2015 to 2017Enrolled40ConditionsAdvanced Hepatocellular CarcinomaArmsPIK-PD-1 cells, DC-PMAT
NCT02632019 phase1 / phase2unknown statusnot on this mapstarted 2015, after this paper: background citation

A Clinical Study of Adoptive Cellular Immunotherapy Using Precision T Cells Specific to Personalized Neo-antigen in Treating Patients With Advanced Malignant Tumor of Biliary Tract

TypeinterventionalSponsorSecond Military Medical UniversityRan2015 to 2017Enrolled40ConditionsAdvanced Biliary Tract Malignant TumorArmsGemcitabine, Dendritic cell-precision T cell for neo-antigen combined with gemcitabine treatment
NCT02632188 phase1 / phase2unknown statusnot on this mapstarted 2015, after this paper: background citation

A Controlled Clinic Trial to Survey the Outcome of Immunotherapy Using Precision T Cells Specific to Multiple Common Tumor-Associated Antigen in Treating Patients Underwent Radical Surgery for Hepatocellular Carcinoma

TypeinterventionalSponsorSecond Military Medical UniversityRan2015 to 2017Enrolled60ConditionsLiver CancerArmsPostoperative routine treatment, DC-PMAT treatment
NCT02632201 phase1 / phase2unknown statusnot on this mapstarted 2015, after this paper: background citation

A Clinical Study of Adoptive Cellular Immunotherapy Using Pluripotent Killer T Cells Expressing Antibodies for Human Epidermal Growth Factor Receptor-2 (HER2) in Treating Patients With HER2-Positive Advanced Gastric Cancer With Liver Metastasis

TypeinterventionalSponsorSecond Military Medical UniversityRan2015 to 2017Enrolled40ConditionsLiver Metastasis, Gastric CancerArmsPIK-HER2, DC-PMAT
NCT02638857 phase1 / phase2unknown statusnot on this mapstarted 2015, after this paper: background citation

A Controlled Clinic Trial of Immunotherapy Using Precision T Cells Specific to Multiple Common Tumor-Associated Antigen in Combination With Transcatheter Arterial Chemoembolization in Treating Patients With Advanced Hepatocellular Carcinoma

TypeinterventionalSponsorSecond Military Medical UniversityRan2015 to 2017Enrolled60ConditionsRecurrence Hepatocellular Carcinoma, Advanced Hepatocellular CarcinomaArmsTACE, Dendritic Cell, lipiodol, Mitomycin (MMC), Epirubicin(EADM)
3 · Its place in the literature

Who cites it

30 citing papers in PubMed, 1 synthesis or guideline pooled it, 69 citations in OpenAlex.

  1. Pooled it
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  17. Therapeutic vaccines for gastrointestinal cancers.Gastroenterology & hepatology · 2011
    Article
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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

10 authors at 2 institutions in 1 country.

Jana BabatzMedizinische Klinik und Poliklinik I, Universitätsklinikum Dresden, Fetscherstr. 74, 01307, Dresden, Germany.
Christoph Röllig
Bärbel Löbel
Gunnar Folprecht
Michael Haack
Heinrich Günther
Claus-Henning Köhne
Gerhard Ehninger
Marc Schmitz
Martin Bornhäuser
Klinik und Poliklinik für Psychotherapie und Psychosomatik · DETU Dresden · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeDendritic cells (DCs) are characterized by their extraordinary capacity to induce T-cell responses, providing the opportunity of DC-based cancer vaccination protocols. In the present study, we conducted a phase I/II clinical trial to determine the capability of DCs differentiated from immunomagnetically isolated CD14+ monocytes and pulsed with a carcinoembryonic antigen-derived altered peptide (CEAalt) to induce specific CD8+ T cells in cancer patients. EXPERIMENTAL

designNine patients with CEA-positive colorectal cancer (n=7) or lung cancer (n=2) were enrolled in this study. Autologous CD14+ monocytes were isolated by large-scale immunomagnetic separation and differentiated to mature DCs in sufficient numbers and at high purity. After incubation with the CEAalt peptide and keyhole limpet hemocyanin, DCs were administered to patients intravenously at dose levels of 1 x 10(7) and 5 x 10(7) cells. Patients received four immunizations every second week.

resultsELISPOT analysis revealed a vaccine-induced increase in the number of CEAalt peptide-specific Interferon (IFN)-gamma producing CD8+ T cells in five of nine patients and of CD8+ T lymphocytes recognizing the native CEA peptide in three of nine patients. In addition, CD8+ T lymphocytes derived from one patient exhibiting an immunological response after vaccination efficiently lysed peptide-loaded T2 cells and tumor cells. Immunization was well tolerated by all patients without severe signs of toxicity.

conclusionVaccination with CEAalt-pulsed DCs derived from immunomagnetically isolated CD14+ monocytes efficiently expand peptide-specific CD8+ T lymphocytes in vivo and may be a promising alternative for cancer immunotherapy.

Indexed as

AdultCancer VaccinesCarcinoembryonic AntigenCD8-Positive T-LymphocytesCell DifferentiationColorectal NeoplasmsDendritic CellsFemaleFlow CytometryHumansImmunity, CellularImmunomagnetic SeparationInterferon-gammaLigandsLipopolysaccharide ReceptorsLung NeoplasmsCancer VaccinesCarcinoembryonic AntigenInterferon-gammaLigandsLipopolysaccharide ReceptorsPeptides

Identifiers

PMID16034561
PMCPMC11031026
OpenAlexW2010120404

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.