Evidence map›Paper›PMID 29600445›Full record

ReviewCancer immunology, immunotherapy : CII2018

Tumor lysate-based vaccines: on the road to immunotherapy for gallbladder cancer.

Daniel Rojas-Sepúlveda, Andrés Tittarelli, María Alejandra Gleisner, Ignacio Ávalos, Cristián Pereda, Iván Gallegos, Fermín Eduardo González, Mercedes Natalia López, Jean Michel Butte, Juan Carlos Roa and 2 more

Open access · hybridAbstract readReview
In one paragraph

Review in Cancer immunology, immunotherapy : CII, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
1.7field-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.

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

31 citing papers in PubMed, 58 citations in OpenAlex.

  1. Review
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  7. Oncology letters · 2024
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  15. Immunology and immunotherapy of cholangiocarcinoma.Nature reviews. Gastroenterology & hepatology · 2023
    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

12 authors at 6 institutions in 1 country.

Daniel Rojas-SepúlvedaDisciplinary Program of Immunology, Institute of Biomedical Sciences, Faculty of Medicine, Universidad de Chile, Independencia 1027, building H, Third floor, 8380453, Santiago, Chile.
Andrés TittarelliDisciplinary Program of Immunology, Institute of Biomedical Sciences, Faculty of Medicine, Universidad de Chile, Independencia 1027, building H, Third floor, 8380453, Santiago, Chile.ORCID http://orcid.org/0000-0003-4129-9734
María Alejandra GleisnerDisciplinary Program of Immunology, Institute of Biomedical Sciences, Faculty of Medicine, Universidad de Chile, Independencia 1027, building H, Third floor, 8380453, Santiago, Chile.
Ignacio ÁvalosDisciplinary Program of Immunology, Institute of Biomedical Sciences, Faculty of Medicine, Universidad de Chile, Independencia 1027, building H, Third floor, 8380453, Santiago, Chile.
Cristián PeredaDisciplinary Program of Immunology, Institute of Biomedical Sciences, Faculty of Medicine, Universidad de Chile, Independencia 1027, building H, Third floor, 8380453, Santiago, Chile.
Iván GallegosPathological Anatomy Service, Clinic Hospital, Universidad de Chile, 8380456, Santiago, Chile.
Fermín Eduardo GonzálezMillennium Institute on Immunology and Immunotherapy, Universidad de Chile, 8380453, Santiago, Chile.
Mercedes Natalia LópezDisciplinary Program of Immunology, Institute of Biomedical Sciences, Faculty of Medicine, Universidad de Chile, Independencia 1027, building H, Third floor, 8380453, Santiago, Chile.
Jean Michel ButteDepartment of Surgery, Fundación Arturo López Pérez, Institute of Oncology, 7500921, Santiago, Chile.
Juan Carlos RoaDepartment of Pathology, School of Medicine, Pontificia Universidad Católica de Chile, 8330023, Santiago, Chile.
Paula FluxáDisciplinary Program of Immunology, Institute of Biomedical Sciences, Faculty of Medicine, Universidad de Chile, Independencia 1027, building H, Third floor, 8380453, Santiago, Chile.
Flavio Salazar-OnfrayDisciplinary Program of Immunology, Institute of Biomedical Sciences, Faculty of Medicine, Universidad de Chile, Independencia 1027, building H, Third floor, 8380453, Santiago, Chile. fsalazar@u.uchile.cl.ORCID http://orcid.org/0000-0002-1848-5697
Millennium Institute on Immunology and Immunotherapy · CLFundación Arturo López Pérez · CLHospital Clínico de la Universidad de Chile · CLPontificia Universidad Católica de Chile · CLSan Sebastián University · CLUniversidad de Santiago de Chile · CL

Funding

CONICYT-PAI/TESIS DOCTORADO SECTOR PRODUCTIVO 7815110008CONICYT-PCHA/Doctorado Nacional 21130465Fondecyt 11160380Fondecyt 1171213FONDECYT POSTDOCTORADO 3170917Fondo de Fomento al Desarrollo Científico y Tecnológico ID16i10148Fondo de Fomento al Desarrollo Científico y Tecnológico MIII P09/016-F
6 · The paper itself

Abstract

Immunotherapy based on checkpoint blockers has proven survival benefits in patients with melanoma and other malignancies. Nevertheless, a significant proportion of treated patients remains refractory, suggesting that in combination with active immunizations, such as cancer vaccines, they could be helpful to improve response rates. During the last decade, we have used dendritic cell (DC) based vaccines where DCs loaded with an allogeneic heat-conditioned melanoma cell lysate were tested in a series of clinical trials. In these studies, 60% of stage IV melanoma DC-treated patients showed immunological responses correlating with improved survival. Further studies showed that an essential part of the clinical efficacy was associated with the use of conditioned lysates. Gallbladder cancer (GBC) is a high-incidence malignancy in South America. Here, we evaluated the feasibility of producing effective DCs using heat-conditioned cell lysates derived from gallbladder cancer cell lines (GBCCL). By characterizing nine different GBCCLs and several fresh tumor tissues, we found that they expressed some tumor-associated antigens such as CEA, MUC-1, CA19-9, Erb2, Survivin, and several carcinoembryonic antigens. Moreover, heat-shock treatment of GBCCLs induced calreticulin translocation and release of HMGB1 and ATP, both known to act as danger signals. Monocytes stimulated with combinations of conditioned lysates exhibited a potent increase of DC-maturation markers. Furthermore, conditioned lysate-matured DCs were capable of strongly inducing CD4

Indexed as

AnimalsAntigens, NeoplasmBiomarkersCancer VaccinesCell Line, TumorDendritic CellsGallbladder NeoplasmsGene Expression RegulationHeat-Shock ResponseHumansImmunotherapyLymphocyte ActivationMacrophagesMonocytesT-LymphocytesAntigens, NeoplasmBiomarkersCancer VaccinesCITIM 2017Dendritic cellsGallbladder cancerImmunotherapyMelanomaTumor lysates

Identifiers

PMID29600445
PMCPMC6244977
OpenAlexW2795611717

What OpenQuestion holds

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LicenceCC BY
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.