Evidence map›Paper›PMID 26676223›Full record

Trial reportJournal of veterinary pharmacology and therapeutics2016

Effects of oral cyclosporine on canine T-cell expression of IL-2 and IFN-gamma across a 12-h dosing interval.

C L Fellman, T M Archer, J V Stokes, R W Wills, K V Lunsford, A J Mackin

Open access · greenAbstract readClinical Trial
In one paragraph

Trial report in Journal of veterinary pharmacology and therapeutics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

14 citing papers in PubMed, 25 citations in OpenAlex.

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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

6 authors at 1 institution in 1 country.

C L FellmanDepartment of Clinical Sciences, College of Veterinary Medicine, Mississippi State University, Mississippi State, MS, USA.
T M ArcherDepartment of Clinical Sciences, College of Veterinary Medicine, Mississippi State University, Mississippi State, MS, USA.
J V StokesDepartment of Basic Sciences, College of Veterinary Medicine, Mississippi State University, Mississippi State, MS, USA.
R W WillsDepartment of Pathobiology and Population Medicine, College of Veterinary Medicine, Mississippi State University, Mississippi State, MS, USA.
K V LunsfordDepartment of Clinical Sciences, College of Veterinary Medicine, Mississippi State University, Mississippi State, MS, USA.
A J MackinDepartment of Clinical Sciences, College of Veterinary Medicine, Mississippi State University, Mississippi State, MS, USA.
Mississippi State University · US

Funding

Summer Research Experience for Veterinary StudentsT35OD010432 · OD · MISSISSIPPI STATE UNIVERSITY · PI Barbara Lee-Faubert Kaplan, Temesgen Samuel · 2012 to 2026
$1.3M
NIH HHS T35 OD010432
6 · The paper itself

Abstract

The duration of immunosuppressive effects following oral cyclosporine in dogs is unknown. This study used flow cytometry and quantitative reverse transcription-polymerase chain reaction (qRT-PCR) to evaluate the effects of high-dose oral cyclosporine across a 12-h dosing interval. Expression of interleukin-2 (IL-2) and interferon-gamma (IFN-γ) was compared before and after 8 days of cyclosporine at 10 mg/kg every 12 h in six healthy dogs. Samples were collected at 0, 2, 4, and 8 h postdosing for analysis of unactivated and activated T-cell and whole blood cytokine expression using flow cytometry and qRT-PCR, respectively, and at 0, 2, 4, 6, 8, and 10 h postdosing for measurement of cyclosporine concentrations. Flow cytometry and qRT-PCR both demonstrated significant marked reductions in IL-2 and IFN-γ levels at 0, 2, 4, and 8 h after dosing compared to pretreatment levels (P < 0.05) for activated samples, with less consistent effects observed for unactivated samples. Both flow cytometry and qRT-PCR are viable techniques for measuring cyclosporine pharmacodynamics in dogs, yielding comparable results with activated samples. Two hours postdrug administration is the preferred time for concurrent assessment of peak drug concentration and cytokine expression, and T-cell activation is needed for optimal results.

Indexed as

DogsAdministration, OralAnimalsCyclosporineDrug Administration ScheduleFlow CytometryGene Expression RegulationImmunosuppressive AgentsInterferon-gammaInterleukin-2Lymphocyte ActivationReal-Time Polymerase Chain ReactionTetradecanoylphorbol AcetateT-LymphocytesCyclosporineImmunosuppressive AgentsInterferon-gammaInterleukin-2Tetradecanoylphorbol Acetate

Identifiers

PMID26676223
PMCPMC4834224
OpenAlexW2255538883

What OpenQuestion holds

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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.