Evidence map›Paper›PMID 26582907›Full record

ArticleStem cells translational medicine2016

Therapeutic Efficacy of Fresh, Autologous Mesenchymal Stem Cells for Severe Refractory Gingivostomatitis in Cats.

Boaz Arzi, Emily Mills-Ko, Frank J M Verstraete, Amir Kol, Naomi J Walker, Megan R Badgley, Nasim Fazel, William J Murphy, Natalia Vapniarsky, Dori L Borjesson

Open access · goldAbstract read
In one paragraph

Article in Stem cells translational medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 78 papers.

0numbers the graph read from it
0cells of the map it votes in
78citing papers in PubMed
10.0field-weighted citation impact, top 1% 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

78 citing papers in PubMed, 134 citations in OpenAlex.

  1. Trial
  2. Review
  3. The Biodistribution ofVeterinary sciences · 2026
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  13. The prevalence of reasons for tooth extraction in cats.Frontiers in veterinary science · 2025
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18 more citing papers are in PubMed but not listed here.

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

10 authors at 2 institutions in 1 country.

Boaz ArziDepartment of Surgical and Radiological Sciences, University of California, Davis, Davis, California, USA barzi@ucdavis.edu.
Emily Mills-KoDepartment of Pathology, Microbiology and Immunology, School of Veterinary Medicine, University of California, Davis, Davis, California, USA.
Frank J M VerstraeteDepartment of Surgical and Radiological Sciences, University of California, Davis, Davis, California, USA.
Amir KolDepartment of Pathology, Microbiology and Immunology, School of Veterinary Medicine, University of California, Davis, Davis, California, USA.
Naomi J WalkerDepartment of Pathology, Microbiology and Immunology, School of Veterinary Medicine, University of California, Davis, Davis, California, USA.
Megan R BadgleyWilliam R. Pritchard Veterinary Medical Teaching Hospital, University of California, Davis, Davis, California, USA.
Nasim FazelDepartment of Dermatology, School of Medicine, University of California, Davis, Davis, California, USA.
William J MurphyDepartment of Dermatology, School of Medicine, University of California, Davis, Davis, California, USA.
Natalia VapniarskyDepartment of Biomedical Engineering, University of California, Davis, Davis, California, USA.
Dori L BorjessonDepartment of Pathology, Microbiology and Immunology, School of Veterinary Medicine, University of California, Davis, Davis, California, USA.
University of California, Davis · USVeterinary Medical Teaching Hospital · US

Funding

Comparative Medical Science Training ProgramT32OD011147 · OD · UNIVERSITY OF CALIFORNIA AT DAVIS · PI JEROEN SAEIJ, Sara Michelle Thomasy · 2012 to 2026
$5.5M
An Animal Model of Chronic Oral Inflammation for Stem Cell-Based TherapyR21DE024711 · NIDCR · UNIVERSITY OF CALIFORNIA AT DAVIS · PI BORJESSON, DORI L. · 2014 to 2015
$312k
NIDCR NIH HHS 1R21DE024711-01NIDCR NIH HHS R21 DE024711NIH HHS T32 OD011147
6 · The paper itself

Abstract

unlabelledMesenchymal stem cells (MSCs) are a promising therapy for immune-mediated and inflammatory disorders, because of their potent immunomodulatory properties. In this study, we investigated the use of fresh, autologous, adipose-derived MSCs (ASCs) for feline chronic gingivostomatitis (FCGS), a chronic, debilitating, idiopathic, oral mucosal inflammatory disease. Nine cats with refractory FCGS were enrolled in this pilot study. Each cat received 2 intravenous injections of 20 million autologous ASCs, 1 month apart. Oral biopsies were taken before and at 6 months after the first ASC injection. Blood immune cell subsets, serum protein, and cytokine levels were measured at 0, 1, 3, and 6 months after treatment to assess immunomodulatory effects. Seven of the 9 cats completed the study. Five cats responded to treatment by either complete clinical remission (n=3) or substantial clinical improvement (n=2). Two cats were nonresponders. Cats that responded to treatment also exhibited systemic immunomodulation demonstrated by decreased numbers of circulating CD8+ T cells, a normalization of the CD4/CD8 ratio, decreased neutrophil counts, and interferon-γ and interleukin (IL)-1β concentration, and a temporary increase in serum IL-6 and tumor necrosis factor-α concentration. No clinical recurrence has occurred following complete clinical remission (follow-up of 6-24 months). In this study, cats with <15% cytotoxic CD8 T cells with low expression of CD8 (CD8lo) cells were 100% responsive to ASC therapy, whereas cats with >15% CD8lo cells were nonresponders. The relative absence of CD8lo cells may be a biomarker to predict response to ASC therapy, and may shed light on pathogenesis of FCGS and mechanisms by which ASCs decrease oral inflammation and affect T-cell phenotype. SIGNIFICANCE: This study is the first to demonstrate the safety and efficacy of fresh, autologous, adipose-derived stem cell systemic therapy for a naturally occurring, chronic inflammatory disease in cats. The findings demonstrate that this therapy resulted in complete clinical and histological resolution or reduction in clinical disease severity and immune modulation in most cats. This study also identified a potentially useful biomarker that could dictate patient enrollment and shed light on immune modulation mechanism. As a naturally occurring animal model, FCGS also provides a strategic platform for potentially translatable therapy for the treatment of human oral inflammatory disease.

Indexed as

Mesenchymal Stem Cell TransplantationStomatitisAnimalsAutograftsCat DiseasesCatsFemaleHumansMaleMesenchymal Stem CellsAdipose-derived stem cellsAutologousCatsFreshGingivostomatitisImmunomodulationOral mucosa

Identifiers

PMID26582907
PMCPMC4704876
OpenAlexW2208981157

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.