Harley R, Helps C R, Harbour D A, Gruffydd-Jones T J, Day M J
Department of Clinical Veterinary Science, University of Bristol, Langford, Bristol BS40 5DU, United Kingdom.
Clin Diagn Lab Immunol. 1999 Jul;6(4):471-8. doi: 10.1128/CDLI.6.4.471-478.1999.
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.
已开发出半定量逆转录聚合酶链反应(RT-PCR)检测方法,用于测量猫口腔黏膜活检组织中猫白细胞介素-2(IL-2)、IL-4、IL-5、IL-6、IL-10和IL-12(p35和p40);γ干扰素(IFN-γ);以及甘油醛-3-磷酸脱氢酶mRNA的浓度。在30只患有慢性龈口炎(患病)的猫接受四种治疗之一之前,采集其活检组织。在23例病例中,在治疗开始3个月后采集重复活检组织。还对11只无临床疾病(未患病)的猫的活检组织进行了分析。在大多数未患病的活检组织中检测到IL-2、IL-10、IL-12(p35和p40)和IFN-γ的表达,而少数检测到IL-6的表达,IL-4和IL-5均未检测到。与未患病的猫相比,患病群体中IL-2、IL-4、IL-6、IL-10、IL-12(p35和p40)和IFN-γ的相对mRNA表达显著增加。相比之下,IL-5 mRNA表达未改变,仅在1例中检测到。在治疗期间,特定细胞因子mRNA相对表达的变化与局部黏膜病变临床严重程度的变化之间未显示出显著关系。结果表明,正常猫口腔黏膜倾向于主要为细胞因子表达的1型(Th)模式,并且在猫慢性龈口炎中所见病变的发展过程中,细胞因子模式从1型转变为1型和2型混合反应。