Kolopp-Sarda M N, Moneret-Vautrin D A, Gobert B, Kanny G, Brodschii M, Bene M C, Faure G C
Laboratoire d'Immunologie, Faculté de Médecine & CHU de Nancy, Vandoeuvre-les-Nancy, France.
Clin Exp Allergy. 1997 Nov;27(11):1285-91.
Hypersensitivity to sesame seeds is becoming increasingly frequent, probably owing to the larger use of this compound in international food.
This study investigated serum responses of 12 sesame sensitized patients (seven with food allergy, five with food sensitization), to a sesame protein extract, and attempted at identifying sesame major antigens.
Sesame protein extracts were prepared from black, white and brown sesame seeds. Electrophoretic analysis showed similar protein patterns in the three extracts, and proper preservation of the proteins integrity. The brown sesame extract was used to set-up an ELISA assay and measure serum levels of antisesame IgG, IgA, IgM and IgE in 12 samples from sesame-sensitized individuals and six controls. It also allowed to perform western blot analyses in order to investigate the molecular weight of sesame proteins recognized by IgG, IgA and IgE.
Nineteen protein bands were observed upon polyacrylamide gel electrophoresis of the sesame protein extracts. Using this whole extract in ELISA, significant antisesame IgG, IgA and IgE-responses were observed in the serum of sensitized individuals, different from the lower signals obtained with control samples. Western blot analysis demonstrated highly polymorphic IgG and IgA responses and a more restricted IgE response pattern, suggesting that two proteins, respectively, 14 kDa and 25 kDa are mostly involved in sesame IgE-dependent hypersensitivity, the 25 kDa band presenting several characteristics of a major allergen.
This study reports novel information on the possible involvement of a 25 kDa sesame protein in IgE-dependent hypersensitivity to sesame seeds.
对芝麻籽的过敏反应越来越常见,这可能是由于该成分在国际食品中的使用量增加。
本研究调查了12名芝麻过敏患者(7名食物过敏患者,5名食物敏感患者)对芝麻蛋白提取物的血清反应,并试图鉴定芝麻的主要抗原。
从黑芝麻、白芝麻和棕芝麻中制备芝麻蛋白提取物。电泳分析表明,三种提取物中的蛋白质模式相似,且蛋白质完整性得到妥善保存。使用棕芝麻提取物建立酶联免疫吸附测定(ELISA),并检测12份芝麻过敏个体样本和6份对照样本中的抗芝麻IgG、IgA、IgM和IgE的血清水平。同时,还进行了蛋白质印迹分析,以研究IgG、IgA和IgE识别的芝麻蛋白的分子量。
芝麻蛋白提取物经聚丙烯酰胺凝胶电泳后观察到19条蛋白带。在ELISA中使用这种全提取物时,在过敏个体的血清中观察到显著的抗芝麻IgG、IgA和IgE反应,与对照样本获得的较低信号不同。蛋白质印迹分析显示IgG和IgA反应具有高度多态性,而IgE反应模式更为局限,这表明分别为14 kDa和25 kDa的两种蛋白质主要参与芝麻IgE依赖性过敏反应,25 kDa条带具有主要过敏原的几个特征。
本研究报告了关于一种25 kDa芝麻蛋白可能参与芝麻籽IgE依赖性过敏反应的新信息。