Evidence map›Paper›PMID 27856424›Full record

ArticleCancer immunology research2016

Eradication of Canine Diffuse Large B-Cell Lymphoma in a Murine Xenograft Model with CD47 Blockade and Anti-CD20.

Kipp Weiskopf, Katie L Anderson, Daisuke Ito, Peter J Schnorr, Hirotaka Tomiyasu, Aaron M Ring, Kristin Bloink, Jem Efe, Sarah Rue, David Lowery and 8 more

Open access · greenAbstract read
In one paragraph

Article in Cancer immunology research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

29 citing papers in PubMed, 57 citations in OpenAlex.

  1. Review
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  4. Article
  5. Article
  6. Review
  7. Review
  8. Racing CARs to veterinary immuno-oncology.Frontiers in veterinary science · 2023
    Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Review
  15. Review
  16. Current Advances inFrontiers in pharmacology · 2021
    Review
  17. Article
  18. Article
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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

18 authors at 5 institutions in 2 countries.

Kipp WeiskopfInstitute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, California. modiano@umn.edu kweiskopf@bwh.harvard.edu.
Katie L AndersonDepartment of Veterinary Clinical Sciences, University of Minnesota, St. Paul, Minnesota.
Daisuke ItoDepartment of Veterinary Clinical Sciences, University of Minnesota, St. Paul, Minnesota.
Peter J SchnorrInstitute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, California.
Hirotaka TomiyasuDepartment of Veterinary Clinical Sciences, University of Minnesota, St. Paul, Minnesota.
Aaron M RingInstitute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, California.
Kristin BloinkElanco Animal Health US, Inc., Greenfield, Indiana.
Jem EfeGenomics Institute of the Novartis Research Foundation, San Diego, California.
Sarah RueGenomics Institute of the Novartis Research Foundation, San Diego, California.
David LoweryElanco Animal Health US, Inc., Greensboro, North Carolina.
Amira BarkalInstitute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, California.
Susan ProhaskaInstitute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, California.
Kelly M McKennaInstitute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, California.
Ingrid CornaxMasonic Cancer Center, University of Minnesota, Minneapolis, Minnesota.
Timothy D O'BrienMasonic Cancer Center, University of Minnesota, Minneapolis, Minnesota.
M Gerard O'SullivanMasonic Cancer Center, University of Minnesota, Minneapolis, Minnesota.
Irving L WeissmanInstitute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, California.
Jaime F ModianoDepartment of Veterinary Clinical Sciences, University of Minnesota, St. Paul, Minnesota. modiano@umn.edu kweiskopf@bwh.harvard.edu.
California Institute for Regenerative Medicine · USUniversity of Minnesota · USGenomics Institute of the Novartis Research Foundation · USUnited Animal Health (United States) · USUniversity of North Carolina at Greensboro · US

Funding

Women's CancerP30CA077598 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI Jeffrey S. Miller · 1998 to 2026
$100.4M
MEDICAL SCIENTIST TRAINING PROGRAMT32GM007365 · NIGMS · STANFORD UNIVERSITY · PI CHUA, KATRIN F · 1985 to 2021
$33.8M
therapeutic Targeting of CD47 on Human Leukemia and Other Cancer Stem CellsP01CA139490 · NCI · STANFORD UNIVERSITY · PI CLARKE, MICHAEL · 2009 to 2013
$8.7M
Sensitization to CD47 Blockade to Enhance Anti-Tumor ImmunityF30CA195973 · NCI · UNIVERSITY OF MINNESOTA · PI ANDERSON, KATIE LYNNE · 2015 to 2018
$177k
EVOLVING HIGH AFFINITY SIRPa MUTANTS TO STIMULATE PHAGOCYTOSIS OF TUMOR CELLSF30CA168059 · NCI · STANFORD UNIVERSITY · PI WEISKOPF, KIPP A · 2012 to 2014
$142k
NCI NIH HHS F30 CA168059NCI NIH HHS F30 CA195973NCI NIH HHS P01 CA139490NCI NIH HHS P30 CA077598NIGMS NIH HHS T32 GM007365
6 · The paper itself

Abstract

Cancer immunotherapies hold much promise, but their potential in veterinary settings has not yet been fully appreciated. Canine lymphomas are among the most common tumors of dogs and bear remarkable similarity to human disease. In this study, we examined the combination of CD47 blockade with anti-CD20 passive immunotherapy for canine lymphoma. The CD47/SIRPα axis is an immune checkpoint that regulates macrophage activation. In humans, CD47 is expressed on cancer cells and enables evasion from phagocytosis. CD47-blocking therapies are now under investigation in clinical trials for a variety of human cancers. We found the canine CD47/SIRPα axis to be conserved biochemically and functionally. We identified high-affinity SIRPα variants that antagonize canine CD47 and stimulate phagocytosis of canine cancer cells in vitro When tested as Fc fusion proteins, these therapeutic agents exhibited single-agent efficacy in a mouse xenograft model of canine lymphoma. As robust synergy between CD47 blockade and tumor-specific antibodies has been demonstrated for human cancer, we evaluated the combination of CD47 blockade with 1E4-cIgGB, a canine-specific antibody to CD20. 1E4-cIgGB could elicit a therapeutic response against canine lymphoma in vivo as a single agent. However, augmented responses were observed when combined with CD47-blocking therapies, resulting in synergy in vitro and in vivo and eliciting cures in 100% of mice bearing canine lymphoma. Our findings support further testing of CD47-blocking therapies alone and in combination with CD20 antibodies in the veterinary setting. Cancer Immunol Res; 4(12); 1072-87. ©2016 AACR.

Indexed as

ImmunotherapyAnimalsAntigens, CD20CD47 AntigenCell Line, TumorDogsFemaleImmunoglobulin GLymphoma, Large B-Cell, DiffuseMacrophagesMaleMicePhagocytosisXenograft Model Antitumor AssaysAntigens, CD20CD47 AntigenImmunoglobulin G

Identifiers

PMID27856424
PMCPMC5454476
OpenAlexW2554951495

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.