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Carrier-bound Alt a 1 peptides without allergenic activity for vaccination against Alternaria alternata allergy

机译:无过敏原的携带载体的Alt a 1肽可用于疫苗接种链格孢变应原

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Background The mould Alternaria alternata is a major elicitor of allergic asthma. Diagnosis and specific immunotherapy (SIT) of Alternaria allergy are often limited by the insufficient quality of natural mould extracts.Objective To investigate whether recombinant Alt a 1 can be used for reliable diagnosis of Alternaria alternata allergy and to develop a safe, non-allergenic vaccine for SIT of Alternaria allergy.Methods The qualitative sensitization profile of 80 Alternaria-allergic patients from Austria and Italy was investigated using an allergen micro-array and the amount of Alter-naria-specific IgE directed to rAlt a 1 was quantified by ImmunoCAP measurements. Peptides spanning regions of predicted high surface accessibility of Alt a 1 were synthesized and tested for IgE reactivity and allergenic activity, using sera and basophils from allergic patients. Carrier-bound peptides were studied for their ability to induce IgG antibodies in rabbits which recognize Alt a 1 and inhibit allergic patients' IgE reactivity to Alt a 1.Results rAlt a 1 allowed diagnosis of Alternaria allergy in all tested patients, bound the vast majority (i.e. >95%) of Alternaria-specific IgE and elicited basophil activation already at a concentration of 0.1 ng/mL. Four non-allergenic peptides were synthesized which, after coupling to the carrier protein keyhole limpet hemocyanin, induced Alt a 1-specific IgG and inhibited allergic patients' IgE binding to Alt a 1.Conclusions and clinical relevance rAlt a 1 is a highly allergenic molecule allowing sensitive diagnosis of Alternaria allergy. Carrier-bound non-allergenic Alt a 1 peptides are candidates for safe SIT of Alternaria allergy.
机译:背景霉菌链格孢菌是过敏性哮喘的主要诱因。天然霉菌提取物的质量不足常常限制了交链孢霉变种的诊断和特异性免疫疗法(SIT)。目的探讨重组Alt a 1是否可用于可靠诊断交链孢霉变种,并开发一种安全的,非致敏疫苗方法使用变应原微阵列研究了来自奥地利和意大利的80例过敏性链球菌过敏患者的定性致敏特征,并通过ImmunoCAP测量定量了针对rAlt a 1的过敏性链球菌特异性IgE的量。使用来自过敏患者的血清和嗜碱性粒细胞,合成了跨越预测为Alt a 1的高表面可及性区域的肽,并测试了IgE反应性和过敏原活性。研究了与载体结合的肽在兔中识别ALT 1并抑制变应性患者对Alt 1的IgE反应性的诱导IgG抗体的能力。结果rAlt 1可在所有接受测试的患者中诊断出Alternaria变态反应,占绝大多数(即> 95%)的链格孢菌特异性IgE,并已经以0.1 ng / mL的浓度引起嗜碱性粒细胞活化。合成了四种非变应原性肽,这些肽与载体蛋白匙孔戚血蓝蛋白偶联后,诱导了Alt a 1特异性IgG并抑制了过敏患者与Alt a 1的IgE结合。结论和临床意义rAlt a 1是一种高度致敏分子。可以敏感地诊断出Alternaria过敏。携带者绑定的非变应原性Alt a 1肽是安全治疗链格孢变应原的候选药物。

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