[复发性气道阻塞(RAO)的遗传学]。

V Gerber, J E Swinburne, S C Blott, P Nussbaumer, A Ramseyer, J Klukowska-Rötzler, G Dolf, E Marti, D Burger, T Leeb
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引用次数: 0

摘要

复发性气道阻塞(RAO)是一种多因素、多基因的疾病。受影响的马通常为7岁或以上,表现为运动不耐受,呼吸困难,咳嗽,气道中性粒细胞增多,粘液积聚和高反应性以及胆碱能支气管痉挛。环境因素主要是干草粉尘中的过敏原和刺激物,但RAO的免疫学机制尚不清楚。一些研究已经证明了RAO的易感性,现在已经证明该疾病具有遗传基础。在后代中,当父母一方受到影响时,患RAO的风险增加3倍,当父母双方都患有RAO时,患RAO的风险增加近5倍。对两个高流行家族的分离分析表明,遗传力高,具有多主基因的复杂遗传。整个基因组可以显示出7个染色体区域与RAO的全染色体显著连锁。在位于特应性候选基因附近的微卫星中,位于13号染色体含有IL4R基因区域的微卫星与一只受RAO影响的种马后代的RAO表型密切相关。此外,马的IgE水平受遗传因素的影响,我们有证据表明,同一种马的rao影响的后代对霉菌过敏原的特异性IgE水平增加。遗传标记的鉴定和最终的责任基因不仅可以改善预防,即早期识别易感个体和避免高风险交配,而且还可以提高我们寻找新的治疗靶点和优化现有治疗方法的能力。
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[Genetics of recurrent airway obstruction (RAO)].

Recurrent airway obstruction (RAO) is a multifactorial and polygenic disease. Affected horses are typically 7 years of age or older and show exercise intolerance, increased breathing effort, coughing, airway neutrophilia, mucus accumulation and hyperreactivity as well as cholinergic bronchospasm. The environmental factors responsible are predominantly allergens and irritants in haydust, but the immunological mechanisms underlying RAO are still unclear. Several studies have demonstrated a familiar predisposition for RAO and it is now proven that the disease has a genetic basis. In offspring, the risk of developing RAO is 3-fold increased when one parent is affected and increases to almost 5-fold when both parents have RAO. Segregation analysis in two high-prevalence families demonstrated a high heritability and a complex inheritance with several major genes. A whole genomescan showed chromosome-wide significant linkage of seven chromosomal regions with RAO. Of the microsatellites, which were located near atopy candidate genes, those in a region of chromosome 13 harboring the IL4R gene were strongly associated with the RAO phenotype in the offspring of one RAO-affected stallion. Furthermore, IgE-levels are influenced by hereditary factors in the horse, and we have evidence that RAO-affected offspring of the same stallion have increased levels of specific IgE against moldspore allergens. The identification of genetic markers and ultimately of the responsible genes will not only allow for an improved prophylaxis, i.e. early identification of susceptible individuals and avoidance of high-risk matings, but also improve our ability to find new therapeutic targets and to optimize existing treatments.

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