Evidence map›Paper›PMID 28925793›Full record

ArticleHuman vaccines & immunotherapeutics2018

Sequential administration of MVA-based vaccines and PD-1/PD-L1-blocking antibodies confers measurable benefits on tumor growth and survival: Preclinical studies with MVA-βGal and MVA-MUC1 (TG4010) in a murine tumor model.

Christelle Remy-Ziller, Christine Thioudellet, Julie Hortelano, Murielle Gantzer, Virginie Nourtier, Marie-Christine Claudepierre, Benoit Sansas, Xavier Préville, Kaïdre Bendjama, Eric Quemeneur and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Human vaccines & immunotherapeutics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed, 33 citations in OpenAlex.

  1. Therapeutic vaccines for NSCLC: From mechanisms to clinical translation.Chinese medical journal pulmonary and critical care medicine · 2026
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  12. Evodiamine suppresses non-small cell lung cancer by elevating CD8Journal of experimental & clinical cancer research : CR · 2020
    Article
  13. Comprehensive analysis of the mechanism and treatment significance of Mucins in lung cancer.Journal of experimental & clinical cancer research : CR · 2020
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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

11 authors at 1 institution in 1 country.

Christelle Remy-Zillera Department of Oncoimmunology , Transgene S.A. , Parc d'Innovation, Illkirch-Graffenstaden , Cedex , France.
Christine Thioudelleta Department of Oncoimmunology , Transgene S.A. , Parc d'Innovation, Illkirch-Graffenstaden , Cedex , France.
Julie Hortelanoa Department of Oncoimmunology , Transgene S.A. , Parc d'Innovation, Illkirch-Graffenstaden , Cedex , France.
Murielle Gantzera Department of Oncoimmunology , Transgene S.A. , Parc d'Innovation, Illkirch-Graffenstaden , Cedex , France.
Virginie Nourtiera Department of Oncoimmunology , Transgene S.A. , Parc d'Innovation, Illkirch-Graffenstaden , Cedex , France.
Marie-Christine Claudepierrea Department of Oncoimmunology , Transgene S.A. , Parc d'Innovation, Illkirch-Graffenstaden , Cedex , France.
Benoit Sansasa Department of Oncoimmunology , Transgene S.A. , Parc d'Innovation, Illkirch-Graffenstaden , Cedex , France.
Xavier Prévillea Department of Oncoimmunology , Transgene S.A. , Parc d'Innovation, Illkirch-Graffenstaden , Cedex , France.
Kaïdre Bendjamaa Department of Oncoimmunology , Transgene S.A. , Parc d'Innovation, Illkirch-Graffenstaden , Cedex , France.ORCID 0000-0003-2185-9116
Eric Quemeneura Department of Oncoimmunology , Transgene S.A. , Parc d'Innovation, Illkirch-Graffenstaden , Cedex , France.
Karola Rittnera Department of Oncoimmunology , Transgene S.A. , Parc d'Innovation, Illkirch-Graffenstaden , Cedex , France.
Transgene (France) · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

TG4010, a Modified Vaccinia virus Ankara (MVA) expressing human mucin1 (MUC1) has demonstrated clinical benefit for patients suffering from advanced non-small cell lung cancer (NSCLC) in combination with chemotherapy. To support its development, preclinical experiments were performed with either TG4010 or β-galactosidase-encoding MVA vector (MVA-βgal) in mice presenting tumors in the lung. Tumor growth was obtained after intravenous injection of CT26 murine colon cancer cells, engineered to express either MUC1 or βgal. Mice showed increased survival rates after repeated intravenous injections of TG4010 or MVA-βgal, compared to an empty MVA control vector. Treatment with MVA vectors led to the accumulation of CD3

Indexed as

AnimalsAntineoplastic Agents, ImmunologicalB7-H1 AntigenCancer VaccinesCarcinoma, Non-Small-Cell LungCell Line, TumorCombined Modality TherapyImmunotherapyInjections, IntravenousMembrane GlycoproteinsMiceMice, Inbred BALB CMucin-1NivolumabProgrammed Cell Death 1 ReceptorTreatment OutcomeAntineoplastic Agents, ImmunologicalB7-H1 AntigenCancer VaccinesMembrane GlycoproteinsMUC1 protein, humanMucin-1NivolumabProgrammed Cell Death 1 ReceptorTG4010immune checkpoint blockadelung cancerModified Vaccinia virus AnkaraPD-1PD-L1TG4010

Identifiers

PMID28925793
PMCPMC5791558
OpenAlexW2755252181

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.