Rodríguez-Perez R, Fernández-Rivas M, González-Mancebo E, Sánchez-Monge R, Díaz-Perales A, Salcedo G
Unidad de Alergia, Fundación Hospital Alcorcon, Madrid, Spain; Unidad de Bioquímica, Departamento de Biotecnología, E.T.S. Ingenieros Agrónomos, Madrid, Spain.
Allergy. 2003 Jul;58(7):635-40. doi: 10.1034/j.1398-9995.2003.00198.x.
Peach is among the main foods causing allergic reactions in the Mediterranean adult population. Only a single peach allergen, named Pru p 3, has been characterized. However, a potential role of profilin has also been suggested in grass pollen-associated allergy to peach.
Complementary DNA clones for two different peach profilin isoforms were obtained by reverse transcriptase polymerase chain reaction using non-degenerated primers. Expression of recombinant peach profilin was performed in Escherichia coli, and confirmed using rabbit polyclonal antibodies to sunflower pollen profilin. Twenty-nine individual sera from patients with peach allergy proved by double-blind, placebo-controlled food challenges (DBPCFC), either with (n = 15) or without (n = 14) specific IgE to Bet v 2, were used in immunodetection assays to test recombinant peach profilin reactivity.
Each peach profilin cDNA included an open reading frame coding for a 131 amino acid protein. The peach profilin isoforms, designated Pru p 4.01 and Pru p 4.02, showed 80% of amino acid sequence identity, and were very similar (>70% identity) to allergenic profilins from plant foods and pollens. Recombinant Pru p 4.01 was expressed in E. coli as a nonfusion protein, displaying the expected molecular size and reacting with anti-profilin antibodies. rPru p 4.01 was recognized by all sera (15 of 15) with specific IgE to Bet v 2, whereas no sera (zero of 14) without IgE to this birch allergen reacted with rPru p 4.01.
Peach profilin Pru p 4 is very closed to other allergenic profilins from plant foods and pollens. A complete correlation between reactivity to rPru p 4 and rBet v 2 has been found in sera from peach allergic patients.
桃子是导致地中海成年人群过敏反应的主要食物之一。目前仅鉴定出一种名为Pru p 3的桃子过敏原。然而,肌动蛋白在与草花粉相关的桃子过敏中也被认为具有潜在作用。
使用非简并引物通过逆转录聚合酶链反应获得两种不同桃子肌动蛋白同工型的互补DNA克隆。重组桃子肌动蛋白在大肠杆菌中表达,并用针对向日葵花粉肌动蛋白的兔多克隆抗体进行确认。通过双盲、安慰剂对照食物激发试验(DBPCFC)确诊的29例桃子过敏患者的个体血清,其中15例对Bet v 2有特异性IgE,14例对Bet v 2无特异性IgE,用于免疫检测试验以测试重组桃子肌动蛋白的反应性。
每个桃子肌动蛋白cDNA包含一个编码131个氨基酸蛋白质的开放阅读框。命名为Pru p 4.01和Pru p 4.02的桃子肌动蛋白同工型显示出80%的氨基酸序列同一性,并且与来自植物性食物和花粉的致敏性肌动蛋白非常相似(>70%同一性)。重组Pru p 4.01在大肠杆菌中作为非融合蛋白表达,显示出预期的分子大小并与抗肌动蛋白抗体反应。所有对Bet v 2有特异性IgE的血清(15/15)均能识别rPru p 4.01,而对这种桦树过敏原无IgE的血清(14/0)均不与rPru p 4.01反应。
桃子肌动蛋白Pru p 4与来自植物性食物和花粉的其他致敏性肌动蛋白非常相似。在桃子过敏患者的血清中发现了对rPru p 4和rBet v 2反应性之间的完全相关性。