Division of Allergy and Clinical Immunology, Department of Medicine, University of Colorado Denver, Aurora, CO 80045, USA.
J Immunol Methods. 2011 Sep 30;372(1-2):65-70. doi: 10.1016/j.jim.2011.06.031. Epub 2011 Jul 18.
It is important to know the contribution of specific allergens to a complex allergenic extract and to have a dependable method to assess the effector activity of an extract specifically depleted of that allergen. We have previously shown that removal of the major peanut allergen, Ara h 2, from a crude peanut extract (CPE) minimally altered the effector activity of the extract. Here we describe in detail the methodology used to generate specific rabbit anti-peptide antibodies to remove a related peanut allergen, Ara h 6, from CPE and describe an improvement in the RBL SX-38 cell assay used to assess the effector activity of treated extracts. Our results show that although Ara h 2 and Ara h 6 can be selectively removed from a CPE, removal of each alone from a CPE had no significant effect on the effector activity. However, removal of Ara h 2 and Ara h 6 together significantly reduced the effector activity of CPE.
了解特定过敏原对复杂过敏原提取物的贡献,并拥有一种可靠的方法来评估特定去除该过敏原的提取物的效应物活性非常重要。我们之前已经表明,从粗花生提取物 (CPE) 中去除主要的花生过敏原 Ara h 2 最小化了提取物的效应物活性。在这里,我们详细描述了生成特异性兔抗肽抗体的方法,以从 CPE 中去除相关的花生过敏原 Ara h 6,并描述了用于评估处理后的提取物效应物活性的 RBL SX-38 细胞测定的改进。我们的结果表明,尽管 Ara h 2 和 Ara h 6 可以从 CPE 中选择性地去除,但单独从 CPE 中去除每种过敏原对效应物活性没有显著影响。然而,Ara h 2 和 Ara h 6 一起去除显著降低了 CPE 的效应物活性。