Koebrich Stefanie, Nett-Mettler Claudia, Wilhelm Sylvia, Favrot Claude
Kleintierpraxis Dr Koebrich and Partner, Neulussheim, Germany.
Vet Dermatol. 2012 Jun;23(3):192-e39. doi: 10.1111/j.1365-3164.2012.01041.x. Epub 2012 Mar 20.
Intradermal testing (IDT) is widely used in veterinary medicine to select allergens for immunotherapy. The recommended concentration for mites is 250 protein nitrogen units (PNU)/mL. It is not known whether healthy dogs responding to this concentration have asymptomatic sensitization or irritation. Furthermore, interbatch and intersupplier variability of allergens has not been fully addressed.
HYPOTHESIS/OBJECTIVES: The incidence of positive IDTs in healthy beagles was recorded and the value of combining these results with serology to differentiate between asymptomatic sensitization and irritancy evaluated. Additionally, the interbatch and intersupplier variability of allergens was assessed.
Seventeen healthy laboratory beagles with no history or clinical signs of canine atopic dermatitis were used.
Intradermal tests were performed with four mite allergens from two suppliers (varying batches). An initial IDT at 250 PNU/mL was used to determine whether decreasing or increasing test concentrations were used in the subsequent titration IDTs. Additionally, two IgE ELISA tests from different manufacturers were performed.
Seven of 17 dogs showed IDT reactions at 250 PNU/mL. There were highly significant allergen interbatch and significant intersupplier correlations and agreement. The associations between the IDT reactions and the IgE serologies statistically identified two groups of dogs: one with positive serology and IDT reactions at 250 PNU/mL; and another with negative serology and IDT reactions.
Our results suggest that dogs that have IDT reactions and positive serology are asymptomatically sensitized, while dogs that react at higher allergen concentrations, but have negative serology, do so as a result of irritant reactions.
皮内试验(IDT)在兽医学中广泛用于选择免疫治疗的过敏原。螨的推荐浓度为250蛋白氮单位(PNU)/mL。尚不清楚对该浓度有反应的健康犬是否存在无症状致敏或刺激反应。此外,过敏原的批次间和供应商间变异性尚未得到充分研究。
假设/目的:记录健康比格犬皮内试验阳性的发生率,并评估将这些结果与血清学相结合以区分无症状致敏和刺激反应的价值。此外,评估过敏原的批次间和供应商间变异性。
使用17只无犬特应性皮炎病史或临床症状的健康实验比格犬。
用来自两个供应商(不同批次)的四种螨过敏原进行皮内试验。最初使用250 PNU/mL的皮内试验来确定在随后的滴定皮内试验中是降低还是增加试验浓度。此外,进行了来自不同制造商的两种IgE ELISA试验。
17只犬中有7只在250 PNU/mL时出现皮内试验反应。过敏原批次间存在高度显著相关性,供应商间存在显著相关性和一致性。皮内试验反应与IgE血清学之间的关联在统计学上确定了两组犬:一组血清学阳性且在250 PNU/mL时出现皮内试验反应;另一组血清学阴性且出现皮内试验反应。
我们的结果表明,皮内试验反应和血清学阳性的犬为无症状致敏,而在较高过敏原浓度下有反应但血清学阴性的犬是由刺激反应引起的。