Evidence map›Paper›PMID 29308327›Full record

ArticleOncoimmunology

Enhancement of antibody-dependent cellular cytotoxicity of cetuximab by a chimeric protein encompassing interleukin-15.

Maria Carmen Ochoa, Luna Minute, Ascensión López, Elisabeth Pérez-Ruiz, Celia Gomar, Marcos Vasquez, Susana Inoges, Iñaki Etxeberria, Inmaculada Rodriguez, Saray Garasa and 4 more

Open access · goldAbstract read
In one paragraph

Article in Oncoimmunology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

16 citing papers in PubMed, 28 citations in OpenAlex.

  1. Review
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  4. PES1 reduces CD8Journal of biomedical science · 2023
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  15. Cytokines in clinical cancer immunotherapy.British journal of cancer · 2019
    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

14 authors at 2 institutions in 1 country.

Maria Carmen OchoaProgram of Immunology and Immunotherapy, Center for Applied Medical Research (CIMA), Pamplona, Spain.
Luna MinuteProgram of Immunology and Immunotherapy, Center for Applied Medical Research (CIMA), Pamplona, Spain.
Ascensión LópezServicio de Inmunología e Inmunoterapia, Clínica Universidad de Navarra, Pamplona, Spain.
Elisabeth Pérez-RuizProgram of Immunology and Immunotherapy, Center for Applied Medical Research (CIMA), Pamplona, Spain.
Celia GomarProgram of Immunology and Immunotherapy, Center for Applied Medical Research (CIMA), Pamplona, Spain.
Marcos VasquezProgram of Immunology and Immunotherapy, Center for Applied Medical Research (CIMA), Pamplona, Spain.
Susana InogesServicio de Inmunología e Inmunoterapia, Clínica Universidad de Navarra, Pamplona, Spain.
Iñaki EtxeberriaProgram of Immunology and Immunotherapy, Center for Applied Medical Research (CIMA), Pamplona, Spain.
Inmaculada RodriguezProgram of Immunology and Immunotherapy, Center for Applied Medical Research (CIMA), Pamplona, Spain.
Saray GarasaProgram of Immunology and Immunotherapy, Center for Applied Medical Research (CIMA), Pamplona, Spain.
Jan-Peter Andreas MayerU3 Pharma GmbH, Planegg, Germany.
Peter WirtzU3 Pharma GmbH, Planegg, Germany.
Ignacio MeleroProgram of Immunology and Immunotherapy, Center for Applied Medical Research (CIMA), Pamplona, Spain.
Pedro BerraondoProgram of Immunology and Immunotherapy, Center for Applied Medical Research (CIMA), Pamplona, Spain.
Navarre Institute of Health Research · ESClinica Universidad de Navarra · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Enhancement of antibody-dependent cellular cytotoxicity (ADCC) may potentiate the antitumor efficacy of tumor-targeted monoclonal antibodies. Increasing the numbers and antitumor activity of NK cells is a promising strategy to maximize the ADCC of standard-of-care tumor-targeted antibodies. For this purpose, we have preclinically tested a recombinant chimeric protein encompassing the sushi domain of the IL15Rα, IL-15, and apolipoprotein A-I (Sushi-IL15-Apo) as produced in CHO cells. The size-exclusion purified monomeric fraction of this chimeric protein was stable and retained the IL-15 and the sushi domain bioactivity as measured by CTLL-2 and Mo-7e cell proliferation and STAT5 phosphorylation in freshly isolated human NK and CD8

Indexed as

antibody-dependent cellular cytotoxicityapolipoprotein A-Icetuximabinterleukin 15NK cellscavenger receptor class B type I

Identifiers

PMID29308327
PMCPMC5749662
OpenAlexW2766223535

What OpenQuestion holds

Textmetadata
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.