Evidence map›Paper›PMID 37852175›Full record

ArticleCell reports. Medicine2023

Unedited allogeneic iNKT cells show extended persistence in MHC-mismatched canine recipients.

Antonia Rotolo, Eoin C Whelan, Matthew J Atherton, Irina Kulikovskaya, Danuta Jarocha, Joseph A Fraietta, Michele M Kim, Eric S Diffenderfer, Keith A Cengel, Martina Piviani and 3 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports. Medicine, 2023. 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
3.1field-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

18 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Facts and Hopes of Chimeric Antigen Receptor-Redirected NK T Cells.Clinical cancer research : an official journal of the American Association for Cancer Research · 2025
    Review
  6. Article
  7. Article
  8. Review
  9. Review
  10. Review
  11. Review
  12. Article
  13. Article
  14. Translational History and Hope of Immunotherapy of Canine Tumors.Clinical cancer research : an official journal of the American Association for Cancer Research · 2024
    Review
  15. Human CD4Immunology · 2024
    Article
  16. Article
  17. Applications and Opportunities for Immune Cell CAR Engineering in Comparative Oncology.Clinical cancer research : an official journal of the American Association for Cancer Research · 2024
    Review
  18. 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

13 authors at 1 institution in 1 country.

Antonia RotoloDepartment of Pathobiology, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA. Electronic address: antonia.rotolo@pennmedicine.upenn.edu.
Eoin C WhelanDepartment of Biomedical Sciences, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Matthew J AthertonDepartment of Biomedical Sciences, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA; Department of Clinical Sciences and Advanced Medicine, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Irina KulikovskayaCenter for Cellular Immunotherapies, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Danuta JarochaCenter for Cellular Immunotherapies, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Joseph A FraiettaCenter for Cellular Immunotherapies, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Michele M KimDepartment of Radiation Oncology, University of Pennsylvania, Philadelphia, PA 19104, USA.
Eric S DiffenderferDepartment of Radiation Oncology, University of Pennsylvania, Philadelphia, PA 19104, USA.
Keith A CengelDepartment of Radiation Oncology, University of Pennsylvania, Philadelphia, PA 19104, USA.
Martina PivianiDepartment of Pathobiology, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Enrico RadaelliDepartment of Pathobiology, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Raimon Duran-StruuckDepartment of Pathobiology, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Nicola J MasonDepartment of Pathobiology, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA; Center for Cellular Immunotherapies, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA. Electronic address: nmason@vet.upenn.edu.
University of Pennsylvania · US

Funding

Stem Cell and Transplantation BiologyU54DK106829 · NIDDK · FRED HUTCHINSON CANCER RESEARCH CENTER · PI DEREK L STIREWALT · 2015 to 2026
$9.1M
Referral Ctr-Animal models of human genetic diseaseP40OD010939 · OD · UNIVERSITY OF PENNSYLVANIA · PI CASAL, MARGRET L · 2012 to 2023
$7.9M
Coordinating Center for Canine Immunotherapy Trials and Correlative StudiesU24CA224122 · NCI · UNIVERSITY OF PENNSYLVANIA · PI LONG, QI, MASON, NICOLA J · 2017 to 2021
$3.6M
Advancing allogeneic CAR-iNKT for the treatment of solid tumors through comparative oncologyU01CA272270 · NCI · UNIVERSITY OF PENNSYLVANIA · PI MASON, NICOLA J · 2022 to 2025
$2.1M
Prognostic and Therapeutic Implications of IFNAR1 Signaling on CAR T Cell Therapy for CancerK08CA252619 · NCI · UNIVERSITY OF PENNSYLVANIA · PI ATHERTON, MATTHEW JOHN · 2021 to 2025
$768k
NCI NIH HHS K08 CA252619NCI NIH HHS U01 CA272270NCI NIH HHS U24 CA224122NIDDK NIH HHS U54 DK106829NIH HHS P40 OD010939
6 · The paper itself

Abstract

Allogeneic invariant natural killer T cells (allo-iNKTs) induce clinical remission in patients with otherwise incurable cancers and COVID-19-related acute respiratory failure. However, their functionality is inconsistent among individuals, and they become rapidly undetectable after infusion, raising concerns over rejection and limited therapeutic potential. We validate a strategy to promote allo-iNKT persistence in dogs, an established large-animal model for novel cellular therapies. We identify donor-specific iNKT biomarkers of survival and sustained functionality, conserved in dogs and humans and retained upon chimeric antigen receptor engineering. We reason that infusing optimal allo-iNKTs enriched in these biomarkers will prolong their persistence without requiring MHC ablation, high-intensity chemotherapy, or cytokine supplementation. Optimal allo-iNKTs transferred into MHC-mismatched dogs remain detectable for at least 78 days, exhibiting sustained immunomodulatory effects. Our canine model will accelerate biomarker discovery of optimal allo-iNKT products, furthering application of MHC-unedited allo-iNKTs as a readily accessible universal platform to treat incurable conditions worldwide.

Indexed as

COVID-19Hematopoietic Stem Cell TransplantationNatural Killer T-CellsAnimalsBiomarkersDogsHumansTransplantation, HomologousBiomarkersallogeneic invariant natural killer Tbiomarkerscanine modeldonor-recipient MHC mismatchdonor selectionoff-the-shelf adoptive cell therapy

Identifiers

PMID37852175
PMCPMC10591065
OpenAlexW4387709202

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.