Thomas Wayne R
University of Western Australia, Telethon Kids Institute, Western Australia, Australia.
Allergol Int. 2015 Oct;64(4):304-11. doi: 10.1016/j.alit.2015.05.004. Epub 2015 Jun 13.
The allergenic load of house dust mite allergy is largely constituted by a few proteins with a hierarchical pattern of allergenicity. The serodominant specificities are the group 1&2 and the group 23 faecal allergens. The collective IgE binding to the group 1&2 allergens can measure unequivocal HDM sensitisation better than HDM extracts although discrepancies have been found in regions with complex acarofauna suggesting a need to investigate the specificity with allergen components. The group 4, 5, 7&21 allergens that each induce responses in about 40% of subjects are mid-tier allergens accounting for most of the remaining IgE binding. Their titres are proportional to the concomitant responses to Der p1&2. Group 2 allergen variants have different antibody binding. Body proteins only occasionally induce sensitisation although a higher prevalence of binding by atopic dermatitis patients provides a new avenue of research. A broad spectrum of IgE binding has been associated with diverse symptoms but not with the severity of asthma which is associated with low IgG antibody. Some allergens such as the group 14 large lipid binding proteins and the recently described proteins Der f 24-33, need further investigation but with the cognoscence that other denominated allergens have been found to be minor sensitisers by comparative quantitative analyses. Scabies is a confounder for diagnosis with extracts, inducing cross-reactive antibodies with Der p 4&20 as is seafood allergy with cross reactivity to Der p 10 a minor HDM allergen. The HDM genome sequence can now be used to verify allelic and paralogous variations.
屋尘螨过敏的变应原负荷主要由少数具有分级变应原性模式的蛋白质构成。血清学上主要的特异性是1类和2类以及23类粪便变应原。与1类和2类变应原的总IgE结合比屋尘螨提取物能更好地明确检测屋尘螨致敏情况,尽管在螨类群落复杂的地区发现了差异,这表明需要用变应原成分研究特异性。4类、5类、7类和21类变应原,每类在约40%的受试者中诱导反应,是中等水平变应原,占其余大部分IgE结合。它们的滴度与对Der p1和2的伴随反应成比例。2类变应原变体有不同的抗体结合。身体蛋白质仅偶尔诱导致敏,尽管特应性皮炎患者的结合率较高提供了一条新的研究途径。广泛的IgE结合与多种症状相关,但与哮喘严重程度无关,哮喘严重程度与低IgG抗体相关。一些变应原,如14类大脂质结合蛋白和最近描述的Der f 24 - 33蛋白,需要进一步研究,但要认识到通过比较定量分析发现其他命名的变应原是次要致敏原。疥疮是提取物诊断的干扰因素,可诱导与Der p 4和20交叉反应的抗体,海鲜过敏也是如此,与Der p 10(一种次要的屋尘螨变应原)有交叉反应。现在可以使用屋尘螨基因组序列来验证等位基因和旁系同源变异。