Birkner T, Rumpold H, Jarolim E, Ebner H, Breitenbach M, Skvaril F, Scheiner O, Kraft D
Institute of General and Experimental Pathology, University of Vienna, Austria.
Allergy. 1990 Aug;45(6):418-26. doi: 10.1111/j.1398-9995.1990.tb01092.x.
Sera from 27 birch pollen-allergic patients who had undergone hyposensitization treatment for 22-41 months were studied by immunoblotting before and after therapy, whereby the levels of IgE, IgG and IgG1-4 antibodies directed against the major allergen Bet v I and minor allergens of birch pollen were monitored. The clinical benefit of immunotherapy (IT) was evaluated using a symptom specific questionnaire. In patients with good clinical response (responders, n = 18), as defined by improvement of symptoms, anti-Bet v I IgE antibodies were found to decrease in 10/18 patients (55.5%), whereas in 6/18 (33.3%) no change and in two cases (11.2%) an increase of specific IgE was observed. In the group of patients with unsatisfactory clinical outcome (non-responders, n = 9), 3/9 patients (33.3%) showed a decrease, 3/9 (33.3%) no change and 3/9 (33.3%) an increase in levels of IgE antibodies directed against Bet v I. In the case of minor allergens, 5/18 responders (27.7%) and 8/9 non-responders (88.8%) showed specific IgE before IT. In the responder group, no increase of specific IgE could be observed after IT. In non-responders, however, an increase of IgE directed against minor allergens was seen in 3/9 patients (33.3%). In all patients, regardless of therapeutical success, IT-induced elevated levels of specific IgG, IgG1 and in particular IgG4 directed against Bet v I were found. Regarding minor allergens, a heterogeneous pattern of IgG responses without significant correlation to clinical benefit was observed. Our results indicate that changes in IgG reactivity patterns against Bet v I and minor allergens, as shown by the immunoblot technique, did not correlate with good or bad clinical outcome.
对27名接受过22至41个月减敏治疗的桦树花粉过敏患者的血清,在治疗前后通过免疫印迹法进行研究,监测针对主要过敏原Bet v I和桦树花粉次要过敏原的IgE、IgG及IgG1 - 4抗体水平。使用症状特异性问卷评估免疫疗法(IT)的临床疗效。在症状改善所定义的临床反应良好的患者(反应者,n = 18)中,发现10/18名患者(55.5%)的抗Bet v I IgE抗体减少,而6/18名患者(33.3%)无变化,2例患者(11.2%)的特异性IgE增加。在临床结果不理想的患者组(无反应者,n = 9)中,3/9名患者(33.3%)的抗Bet v I IgE抗体水平下降,3/9名患者(33.3%)无变化,3/9名患者(33.3%)增加。对于次要过敏原,5/18名反应者(27.7%)和8/9名无反应者(88.8%)在免疫疗法前显示有特异性IgE。在反应者组中,免疫疗法后未观察到特异性IgE增加。然而,在无反应者中,3/9名患者(33.3%)出现针对次要过敏原的IgE增加。在所有患者中,无论治疗是否成功,均发现免疫疗法诱导针对Bet v I的特异性IgG、IgG1尤其是IgG4水平升高。对于次要过敏原,观察到IgG反应模式各异,与临床疗效无显著相关性。我们的结果表明,免疫印迹技术显示的针对Bet v I和次要过敏原的IgG反应模式变化与临床结果的好坏无关。