Duchateau J, Michils A, Lambert J, Gossart B, Casimir G
Immunology Department, Centre Hospitalier Universitaire Brugmann-HUDERF, Université Libre de Bruxelles, Brussels, Belgium.
Clin Exp Allergy. 1998 Jul;28(7):824-33. doi: 10.1046/j.1365-2222.1998.00314.x.
We demonstrated recently that mite-allergic patients differed from healthy controls in the specificity of their IgG antibodies towards mite antigens.
The present study investigates whether these discriminatory IgG responses could be associated with the expression and the evolution of clinical manifestations in allergy to cow's milk proteins.
Antibody specificity was evaluated by comparing IgG-binding to native bovine beta-lactoglobulin (nBLG) and its products of pepsin hydrolysis (dBLG) using a solid-phase enzyme-linked immunosorbent assay (ELISA). Antibody specificity was further investigated in competitive ELISA using streptavidin-biotin technology with purified IgG fractions from selected subjects and specific mouse monoclonals raised against BLG.
IgG antibodies from CM-intolerant or allergic sera (n=222) showed a higher degree of binding to nBLG than to dBLG, while control sera showed similar levels to both nBLG and dBLG (n=99 children/65 adults). Sera from symptomatic patients, wether or not they contained IgE antibodies, demonstrated group-segregating capacities to compete with pooled purified IgG from each clinical class, and with selected murine anti-nBLG monoclonal antibodies for binding to n- and dBLG. Furthermore, this inhibitory capacity shifted dramatically in a small subset (n=14) of children as they developed CM-tolerance.
The IgG responses to BLG of CM-intolerant or allergic patients are very different from those of healthy controls, being characterized not only by increased titres but also similar patterns of modified specificity, including a marked preference for conformational epitopes. Cross-competition experiments confirmed that the restricted specificity was clinically associated, appearing as an immunological signature, which allowed almost complete discrimination between patient groups. This phenomenon is a particularly promising diagnostic feature in this category of young patients where conventional tests usually only document the status of sensitization.
我们最近证明,螨过敏患者与健康对照者对螨抗原的IgG抗体特异性不同。
本研究调查这些有区别的IgG反应是否与牛奶蛋白过敏临床表现的表达及演变相关。
通过使用固相酶联免疫吸附测定(ELISA)比较IgG与天然牛β-乳球蛋白(nBLG)及其胃蛋白酶水解产物(dBLG)的结合,评估抗体特异性。使用链霉亲和素-生物素技术,从选定受试者的纯化IgG组分和针对BLG产生的特异性小鼠单克隆抗体,在竞争性ELISA中进一步研究抗体特异性。
不耐受或过敏血清(n = 222)中的IgG抗体与nBLG的结合程度高于与dBLG的结合程度,而对照血清与nBLG和dBLG的水平相似(n = 99名儿童/65名成人)。有症状患者的血清,无论是否含有IgE抗体,都表现出与每个临床类别中汇集的纯化IgG以及选定的鼠抗nBLG单克隆抗体竞争结合nBLG和dBLG的分组区分能力。此外,在一小部分(n = 14)儿童发展为牛奶耐受时,这种抑制能力发生了显著变化。
不耐受或过敏患者对BLG的IgG反应与健康对照者非常不同,不仅表现为滴度增加,还表现出类似的特异性改变模式,包括对构象表位的明显偏好。交叉竞争实验证实,受限的特异性在临床上具有相关性,表现为一种免疫特征,几乎可以完全区分患者组。在这类年轻患者中,这种现象是一个特别有前景的诊断特征,因为传统检测通常只能记录致敏状态。