Evidence map›Paper›PMID 40443661›Full record

ArticleFrontiers in immunology2025

Single cell atlas of canine natural killer cells identifies distinct circulating and tissue resident gene profiles.

Aryana M Razmara, Marshall Lammers, Sean J Judge, William J Murphy, Cameron E Gaskill, William T N Culp, Alicia A Gingrich, Zachary S Morris, Robert B Rebhun, C Titus Brown and 3 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
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

11 citing papers in PubMed.

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  5. Safety and Feasibility of InfusingbioRxiv : the preprint server for biology · 2026
    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

13 authors.

Aryana M RazmaraDivision of Surgical Oncology, Department of Surgery, University of California Davis School of Medicine, Sacramento, CA, United States.
Marshall LammersDivision of Surgical Oncology, Department of Surgery, University of California Davis School of Medicine, Sacramento, CA, United States.
Sean J JudgeDivision of Surgical Oncology, Department of Surgery, University of California Davis School of Medicine, Sacramento, CA, United States.
William J MurphyDepartment of Dermatology, University of California Davis School of Medicine, Sacramento, CA, United States.
Cameron E GaskillDivision of Surgical Oncology, Department of Surgery, University of California Davis School of Medicine, Sacramento, CA, United States.
William T N CulpDepartment of Surgical and Radiological Sciences, University of California Davis School of Veterinary Medicine, Davis, CA, United States.
Alicia A GingrichDivision of Surgical Oncology, Department of Surgery, University of California Davis School of Medicine, Sacramento, CA, United States.
Zachary S MorrisDepartment of Human Oncology, University of Wisconsin School of Medicine and Public Health, Madison, WI, United States.
Robert B RebhunDepartment of Surgical and Radiological Sciences, University of California Davis School of Veterinary Medicine, Davis, CA, United States.
C Titus BrownDepartment Population Health and Reproduction, University of California Davis School of Veterinary Medicine, Davis, CA, United States.
David M VailDepartment of Medical Sciences, University of Wisconsin School of Veterinary Medicine, Madison, WI, United States.
Michael S KentDepartment of Surgical and Radiological Sciences, University of California Davis School of Veterinary Medicine, Davis, CA, United States.
Robert J CanterDivision of Surgical Oncology, Department of Surgery, University of California Davis School of Medicine, Sacramento, CA, United States.

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
Staff InvestigatorsP30CA093373 · NCI · UNIVERSITY OF CALIFORNIA DAVIS · PI KC KENT LLOYD · 2002 to 2026
$84.9M
Immunomodulation of the Tumor Microenvironment with Molecular Targeted Radiotherapy to Facilitate an Adaptive Anti-Tumor Immune Response to Combined Modality ImmunotherapiesU01CA233102 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI MORRIS, ZACHARY SCOTT, WEICHERT, JAMEY P · 2018 to 2022
$4.0M
Gene Expression Analysis of Dog Natural Killer Cells Following Immunotherapy with Molecularly Targeted Radionuclide therapy or Inhaled IL-15U01CA224166 · NCI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI CANTER, ROBERT J., REBHUN, ROBERT B · 2017 to 2021
$3.0M
UC Davis Comparative Oncology Training ProgramT32CA251007 · NCI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI Robert J. Canter, Xinbin Chen · 2020 to 2026
$1.8M
Shared LSRII Cytometer Equipment Application - UC Davis Stem Cell ProgramS10RR026825 · NCRR · UNIVERSITY OF CALIFORNIA AT DAVIS · PI NOLTA, JAN A. · 2010 to 2010
$500k
Acquisition of Covaris E220 and Sciclone G3 systems for high throughput sequencinS10OD010786 · OD · UNIVERSITY OF CALIFORNIA AT DAVIS · PI COMAI, LUCA · 2012 to 2012
$311k
Gene Expression Analysis of Dog Natural Killer Cells as Immunotherapy TargetR03CA252793 · NCI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI CANTER, ROBERT J. · 2021 to 2022
$157k
Targeting Lung Tissue Resident NK Cells with Inhaled IL-15 and TIGIT Blockade in OsteosarcomaR03CA270854 · NCI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI CANTER, ROBERT J. · 2022 to 2023
$151k
Combining Radiation, Allogeneic Natural Killer Immunotherapy, and PD-L1 blockade in Dogs with Naturally-Occurring MelanomaF30CA275317 · NCI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI RAZMARA, ARYANA · 2023 to 2025
$136k
NCI NIH HHS F30 CA275317NCI NIH HHS P30 CA008748NCI NIH HHS P30 CA093373NCI NIH HHS R03 CA252793NCI NIH HHS R03 CA270854NCI NIH HHS T32 CA251007NCI NIH HHS U01 CA224166NCI NIH HHS U01 CA233102NCRR NIH HHS S10 RR026825NIH HHS S10 OD010786
6 · The paper itself

Abstract

Introduction: Natural killer (NK) cells in mice and humans are key effectors of the innate immune system with complex immunoregulatory functions, and diverse subsets have been identified with distinct characteristics and roles. Companion dogs with spontaneous cancer have been validated as models of human disease, including cancer immunology and immunotherapy, and greater understanding of NK cell heterogeneity in dogs can inform NK biology across species and optimize NK immunotherapy for both dogs and people. Methods: Here, we assessed canine NK cell populations by single-cell RNA sequencing (scRNAseq) across blood, lung, liver, spleen, and placenta with comparison to human NK cells from blood and the same tissues to better characterize the differential gene expression of canine and human NK cells regarding ontogeny, heterogeneity, patterns of activation, inhibition, and tissue residence. Results: Overall, we observed tissue-specific NK cell signatures consistent with immature NK cells in the placenta, mature and activated NK cells in the lung, and NK cells with a mixed activated and inhibited signature in the liver with significant cross-species homology. Discussion: Together, our results point to heterogeneous canine NK populations highly comparable to human NK cells, and we provide a comprehensive atlas of canine NK cells across organs which will inform future cross-species NK studies and further substantiate the spontaneous canine model to optimize NK immunotherapy across species.

Indexed as

Killer Cells, NaturalSingle-Cell AnalysisTranscriptomeAnimalsDogsFemaleGene Expression ProfilingHumansOrgan SpecificityPregnancycanine (dog)comparativeNK cellsingle cell RNA sequencing (scRNAseq)tissue residenttranscriptomics

Identifiers

PMID40443661
PMCPMC12119461

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Registered trials

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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.