Evidence map›Paper›PMID 30482760›Full record

ArticleBlood advances2018

IL-15/IL-15Rα/CD80-expressing AML cell vaccines eradicate minimal residual disease in leukemic mice.

Yimin Shi, Lillia Dincheva-Vogel, Charles E Ayemoba, Jeffrey P Fung, Cristina Bergamaschi, George N Pavlakis, Farzin Farzaneh, Karin M L Gaensler

Open access · goldAbstract read
In one paragraph

Article in Blood advances, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.6field-weighted citation impact, top 34% 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

13 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. Review
  10. Review
  11. Review
  12. Review
  13. Review
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

8 authors at 3 institutions in 2 countries.

Yimin ShiDepartment of Medicine, University of California San Francisco School of Medicine, San Francisco, CA.
Lillia Dincheva-VogelDepartment of Medicine, University of California San Francisco School of Medicine, San Francisco, CA.
Charles E AyemobaDepartment of Medicine, University of California San Francisco School of Medicine, San Francisco, CA.
Jeffrey P FungDepartment of Medicine, University of California San Francisco School of Medicine, San Francisco, CA.
Cristina BergamaschiHuman Retrovirus Section, Vaccine Branch, National Cancer Institute, National Institutes of Health, Frederick, MD; and.
George N PavlakisHuman Retrovirus Section, Vaccine Branch, National Cancer Institute, National Institutes of Health, Frederick, MD; and.
Farzin FarzanehDepartment of Haematological Medicine, Rayne Institute, King's College London, London, United Kingdom.
Karin M L GaenslerDepartment of Medicine, University of California San Francisco School of Medicine, San Francisco, CA.
University of California, San Francisco · USNational Cancer Institute · USKing's College London · GB

Funding

Heterodimeric IL-15 in Cancer ImmunotherapyZIABC010750 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI PAVLAKIS, GEORGE N. · 2009 to 2022
$15.6M
Efficacy and safety of novel CD80 IL15 IL15Ra expressing autologous AML vaccinesR21CA177284 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI GAENSLER, KARIN L · 2013 to 2014
$370k
Biotechnology and Biological Sciences Research Council BB/D014301/1NCI NIH HHS R21 CA177284
6 · The paper itself

Abstract

Engineered autologous acute myeloid leukemia (AML) cells present multiple leukemia-associated and patient-specific antigens and as such hold promise as immunotherapeutic vaccines. However, prior vaccines have not reliably induced effective antileukemic immunity, in part because AML blasts have immune inhibitory effects and lack expression of the critical costimulatory molecule CD80. To enhance induction of leukemia-specific cytolytic activity, 32Dp210 murine AML cells were engineered to express either CD80 alone, or the immunostimulatory cytokine interleukin-15 (IL-15) with its receptor α (IL-15Rα), or heterodimeric IL-15/IL-15Rα together with CD80 and tested as irradiated cell vaccines. IL-15 is a γc-chain cytokine, with unique properties suited to stimulating antitumor immunity, including stimulation of both natural killer and CD8

Indexed as

AnimalsB7-1 AntigenCancer VaccinesCell Line, TumorCell ProliferationDisease Models, AnimalFemaleGenetic VectorsInterleukin-15Interleukin-15 Receptor alpha SubunitLeukemia, Myeloid, AcuteMiceMice, Inbred C3HNeoplasm, ResidualSurvival RateT-LymphocytesB7-1 AntigenCancer VaccinesInterleukin-15Interleukin-15 Receptor alpha Subunit

Identifiers

PMID30482760
PMCPMC6258921
OpenAlexW2903517456

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.