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Clinical and Diagnostic Laboratory Immunology, July 1999, p. 471-478, Vol. 6, No. 4
1071-412X/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.

Cytokine mRNA Expression in Lesions in Cats with Chronic Gingivostomatitis

R. Harley,1,* C. R. Helps,1 D. A. Harbour,1 T. J. Gruffydd-Jones,1 and M. J. Day2

Department of Clinical Veterinary Science1 and Department of Pathology and Microbiology,2 University of Bristol, Langford, Bristol BS40 5DU, United Kingdom

Received 28 August 1998/Returned for modification 13 January 1999/Accepted 15 March 1999

Semiquantitative reverse transcription-PCR assays were developed to measure feline interleukin-2 (IL-2), IL-4, IL-5, IL-6, IL-10, and IL-12 (p35 & p40); gamma interferon (IFN-gamma ); and glyceraldehyde-3-phosphate dehydrogenase mRNA concentrations in biopsies of feline oral mucosa. Biopsies were collected from 30 cats with chronic gingivostomatitis (diseased) prior to each cat receiving one of four treatments. In 23 cases replicate biopsies were collected 3 months after treatment commenced. Biopsies were also analyzed from 11 cats without clinical disease (nondiseased). Expression of IL-2, IL-10, IL-12 (p35 and p40), and IFN-gamma was detected in most nondiseased biopsies, while IL-6 was detected in a minority, and IL-4 and IL-5 were both undetectable. Compared to nondiseased cats, the diseased population showed a significant increase in the relative mRNA expression of IL-2, IL-4, IL-6, IL-10, IL-12 (p35 and p40), and IFN-gamma . In contrast, IL-5 mRNA expression was unchanged and was only detected in one case. No significant relationship was demonstrable between the change in relative expression of specific cytokine mRNA and the change in clinical severity of the local mucosal lesions over the treatment period. The results demonstrate that the normal feline oral mucosa is biased towards a predominantly (Th) type 1 profile of cytokine expression and that during the development of lesions seen in feline chronic gingivostomatitis there is a shift in the cytokine profile from a type 1 to a mixed type 1 and type 2 response.


* Corresponding author. Mailing address: Department of Clinical Veterinary Science, Division of Companion Animals, University of Bristol, Langford House, Langford, Bristol BS40 5DU, United Kingdom. Phone: 44 (0) 117-928-9280. Fax: 44 (0) 117-928-9505. E-mail: R.Harley{at}bris.ac.uk.


Clinical and Diagnostic Laboratory Immunology, July 1999, p. 471-478, Vol. 6, No. 4
1071-412X/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.