Division of Immunopathology, Department of Pathophysiology and Allergy Research, Center for Pathophysiology, Infectiology and Immunology, Medical University of Vienna, Vienna General Hospital, Währinger Gürtel 18-20, Vienna, Austria.
Allergy. 2011 Sep;66(9):1174-82. doi: 10.1111/j.1398-9995.2011.02592.x. Epub 2011 Apr 11.
Subcutaneous injection immunotherapy (SCIT) is considered as antigen-specific and disease-modifying treatment with long-lasting effect.
We used a panel of recombinant grass pollen allergens for analyzing allergen-specific IgE, IgG(1) -IgG(4) , IgM, IgA, and light-chain (kappa, lambda) responses in grass pollen-allergic patients who had received one course of injection immunotherapy (SCIT) with an aluminum hydroxide-adsorbed grass pollen extract or only anti-inflammatory treatment. Serum samples were analyzed before and after 5 months of treatment as well as after 5 years.
After 5 months of SCIT but not of anti-inflammatory treatment, IgG(1) > IgG(4) > IgG(2) > IgA antibody responses using both kappa and lambda light chains specific for major grass pollen allergens (Phl p 1, Phl p 5, Phl p 6, Phl p 2) increased significantly, whereas specific IgM or IgG(3) levels were unaltered. Allergen-dependent basophil degranulation was only inhibited with SCIT sera containing therapy-induced allergen-specific IgG antibodies. Likewise, decreases in Phl p 1- and Phl p 5-specific IgE levels and significant (P<0.001) reduction in symptom and medication scores were found only in the SCIT group but not in the group of patients receiving anti-inflammatory treatment. After 5 years, allergen-specific IgG antibody levels in the SCIT group had returned to baseline levels and there was no significant difference regarding symptoms between the SCIT and non-SCIT groups.
The results from our observational study demonstrate that only SCIT but not anti-inflammatory treatment induces allergen-specific IgG and reduces boosts of allergen-specific IgE production but that one SCIT course was not sufficient to achieve long-term immunological and clinical effects.
皮下注射免疫疗法(SCIT)被认为是一种具有抗原特异性和疾病修饰作用的治疗方法,具有持久的效果。
我们使用一组重组草花粉过敏原来分析接受过一疗程注射免疫疗法(SCIT)的草花粉过敏患者的过敏原特异性 IgE、IgG(1)-IgG(4)、IgM、IgA 和轻链(kappa、lambda)反应,该 SCIT 采用氢氧化铝吸附的草花粉提取物或仅抗炎治疗。在治疗 5 个月前后以及 5 年后分析血清样本。
在接受 SCIT 治疗 5 个月后,但在接受抗炎治疗 5 个月后,针对主要草花粉过敏原(Phl p 1、Phl p 5、Phl p 6、Phl p 2)的特异性 IgG(1)>IgG(4)>IgG(2)>IgA 抗体反应均显著增加,而特异性 IgM 或 IgG(3)水平则保持不变。只有含有治疗诱导的过敏原特异性 IgG 抗体的 SCIT 血清才能抑制过敏原依赖性嗜碱性粒细胞脱颗粒。同样,仅在 SCIT 组中发现 Phl p 1 和 Phl p 5 特异性 IgE 水平下降,症状和药物评分显著(P<0.001)降低,而在接受抗炎治疗的患者组中则没有发现。5 年后,SCIT 组中的过敏原特异性 IgG 抗体水平已恢复到基线水平,并且 SCIT 组和非 SCIT 组之间的症状没有显著差异。
我们的观察性研究结果表明,只有 SCIT 而不是抗炎治疗会诱导过敏原特异性 IgG 并减少过敏原特异性 IgE 产生的增强,但一疗程的 SCIT 不足以实现长期的免疫和临床效果。