Research & Development, Nestlé Purina Research, St Louis, MO, USA.
J Feline Med Surg. 2019 Oct;21(10):875-881. doi: 10.1177/1098612X19861218. Epub 2019 Jul 16.
Fel d1 is the major cat allergen, causing IgE reactions in up to 90% of cat-allergic adults. Fel d1 secreted in saliva is spread to the haircoat during grooming. Current management includes attempts to reduce or eliminate exposure to Fel d1. A novel approach to reducing immunologically active Fel d1 (aFel d1) exposure, which involves binding the Fel d1 with an anti-Fel d1-specific polyclonal egg IgY antibody (sIgY), was evaluated. The hypothesis was that saliva from cats fed diets containing this sIgY would show a significant reduction in aFel d1.
Two trials in cats were completed. In trial 1, saliva was collected 0, 1, 3 and 5 h post-feeding during a 2 week baseline and subsequent 6 week treatment period. Trial 2 included a control and treatment group, and saliva was collected once daily. Trial 2 cats were fed the control diet during a 1 week baseline period, and then fed either control or sIgY diet during the 4 week treatment period. Fel d1-specific ELISA was used to measure salivary aFel d1. Data were analysed using repeated-measures ANOVA and a linear mixed-model analysis.
Salivary aFel d1 decreased post-treatment in both trials. There were no differences in aFel d1 based on time of collection relative to feeding in trial 1. In trial 2, 82% of treatment group cats showed a decrease in aFel d1 of at least 20% from baseline vs just 38% of control cats. Only one (9%) treatment cat showed an increase in aFel d1 vs 63% of control cats.
Feeding sIgY significantly reduced aFel d1 in the saliva of cats within 3 weeks. Although additional research is needed, these findings show promise for an alternative approach to the management of allergies to cats.
Fel d1 是主要的猫过敏原,导致高达 90%的成年猫过敏患者发生 IgE 反应。Fel d1 在唾液中分泌,在梳理过程中散布到被毛上。目前的管理方法包括尝试减少或消除对 Fel d1 的接触。一种新的减少免疫活性 Fel d1(aFel d1)暴露的方法涉及用抗 Fel d1 特异性多克隆卵 IgY 抗体(sIgY)结合 Fel d1,对此方法进行了评估。该假设是,喂食含有这种 sIgY 的饮食的猫的唾液中 aFel d1 会显著减少。
完成了两项猫试验。在试验 1 中,在 2 周基线和随后的 6 周治疗期间,在喂食后 0、1、3 和 5 小时收集唾液。试验 2 包括对照组和治疗组,每天收集一次唾液。在 1 周基线期间,试验 2 的猫喂食对照饮食,然后在 4 周治疗期间喂食对照或 sIgY 饮食。使用 Fel d1 特异性 ELISA 测量唾液中的 aFel d1。使用重复测量方差分析和线性混合模型分析对数据进行分析。
两次试验中,治疗后唾液中的 aFel d1 均减少。在试验 1 中,基于相对于喂食的收集时间,aFel d1 没有差异。在试验 2 中,82%的治疗组猫的 aFel d1 从基线下降至少 20%,而对照组猫仅为 38%。只有 1 只(9%)治疗猫的 aFel d1 增加,而对照组猫为 63%。
在 3 周内,喂食 sIgY 可显著减少猫唾液中的 aFel d1。尽管需要进一步研究,但这些发现为管理猫过敏的替代方法提供了希望。