Evidence map›Paper›PMID 31455682›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2019

Interleukin-15 Enhances Anti-GD2 Antibody-Mediated Cytotoxicity in an Orthotopic PDX Model of Neuroblastoma.

Rosa Nguyen, Ardiana Moustaki, Jacqueline L Norrie, Shantel Brown, Walter J Akers, Abbas Shirinifard, Michael A Dyer

Open access · bronzeAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
3.8field-weighted citation impact, top 6% 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

26 citing papers in PubMed, 1 synthesis or guideline pooled it, 39 citations in OpenAlex.

  1. Pooled it
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  14. Anti-GD2 Antibodies Conjugated to IL15 and IL21 Mediate Potent Antitumor Cytotoxicity against Neuroblastoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2022
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  17. Oncoimmunology · 2022
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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

7 authors at 1 institution in 1 country.

Rosa NguyenDepartment of Oncology, St. Jude Children's Research Hospital, Memphis, Tennessee.
Ardiana MoustakiDepartment of Immunology, St. Jude Children's Research Hospital, Memphis, Tennessee.
Jacqueline L NorrieDevelopmental Neurobiology, St. Jude Children's Research Hospital, Memphis, Tennessee.ORCID 0000-0002-1021-0306
Shantel BrownCenter for In Vivo Imaging and Therapeutics (CIVIT), St. Jude Children's Research Hospital, Memphis, Tennessee.
Walter J AkersCenter for In Vivo Imaging and Therapeutics (CIVIT), St. Jude Children's Research Hospital, Memphis, Tennessee.ORCID 0000-0002-9697-7654
Abbas ShirinifardDevelopmental Neurobiology, St. Jude Children's Research Hospital, Memphis, Tennessee.
Michael A DyerDevelopmental Neurobiology, St. Jude Children's Research Hospital, Memphis, Tennessee. michael.dyer@stjude.org.
St. Jude Children's Research Hospital · US

Funding

Viral Vector Technology (VVTSR)P30CA021765 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI CHARLES ROBERTS · 1985 to 2026
$166.9M
Proliferation Control in the Retina: The Rb FamilyR01EY014867 · NEI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI DYER, MICHAEL A · 2003 to 2012
$4.5M
Proliferation and Differentiation of Retinal Stem CellsR01EY018599 · NEI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI DYER, MICHAEL A · 2008 to 2011
$2.5M
Molecular Targeted Therapy for RetinoblastomaR01CA168875 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI DYER, MICHAEL A · 2012 to 2016
$1.8M
MULTIMODAL PRECLINICAL CANCER IMAGING AND THERAPY RESEARCH SPECIALISTR50CA211481 · NCI · WASHINGTON UNIVERSITY · PI AKERS, WALTER JOHN · 2016 to 2020
$841k
Howard Hughes Medical InstituteNCI NIH HHS P30 CA021765NCI NIH HHS R01 CA168875NCI NIH HHS R50 CA211481NEI NIH HHS R01 EY014867NEI NIH HHS R01 EY018599
6 · The paper itself

Abstract

purposeImmunotherapy with IL2, GM-CSF, and an anti-disialoganglioside (GD2) antibody significantly increases event-free survival in children with high-risk neuroblastoma. However, therapy failure in one third of these patients and IL2-related toxicities pose a major challenge. We compared the immunoadjuvant effects of IL15 with those of IL2 for enhancing antibody-dependent cell-mediated cytotoxicity (ADCC) in neuroblastoma. EXPERIMENTAL

designWe tested ADCC against neuroblastoma patient-derived xenografts (PDX)

resultsIn cell culture, IL15-activated NK cells induced higher ADCC against two GD

conclusionsThe substitution of IL15 for IL2 leads to significant tumor regression

Indexed as

AnimalsAntibodies, MonoclonalAntibody-Dependent Cell CytotoxicityChildFemaleGangliosidesGranulocyte-Macrophage Colony-Stimulating FactorHumansImmunotherapyInterleukin-15Interleukin-2Killer Cells, NaturalNeuroblastomaXenograft Model Antitumor AssaysAntibodies, MonoclonalCSF2 protein, humanganglioside, GD2GangliosidesGranulocyte-Macrophage Colony-Stimulating FactorIL15 protein, humanIL2 protein, humanInterleukin-15Interleukin-2

Identifiers

PMID31455682
PMCPMC6911623
OpenAlexW2970146908

What OpenQuestion holds

Textmetadata
LicenceTDM
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.