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黄蜂毒液的聚集免疫疗法。时间间隔对体内和体外参数影响的评估。

Clustered immunotherapy with Yellow Jacket venom. Evaluation of the influence of time interval on in vivo and in vitro parameters.

作者信息

Malling H J, Djurup R, Søndergaard I, Weeke B

出版信息

Allergy. 1985 Jul;40(5):373-83. doi: 10.1111/j.1398-9995.1985.tb00250.x.

DOI:10.1111/j.1398-9995.1985.tb00250.x
PMID:4037258
Abstract

To evaluate difference in clinical efficacy, side effects, in vivo and in vitro parameters, 25 patients allergic to Yellow Jacket were treated with clustered immunotherapy using either 7 or 14 days interval between clusters. Twenty-one patients completed the 6 months' treatment period and four were withdrawn due to adverse reactions (2 cases of anaphylactic shock). Sixteen patients were challenged by in-hospital sting and the clinical efficacy was complete. Local side effects were observed in the majority of patients, but only rarely limited the course of immunotherapy. Skin sensitivity estimated as the venom concentration eliciting a wheal equal to histamine HCl 0.1 mg/ml using intradermal test was significantly reduced after 6 months of treatment. Specific IgE showed an initial increase, thereafter declining to pretreatment levels. IgG subclasses were determined by a triple antibody assay. Only subclasses 1 and 4 showed response. Subclass 4 showed a steady increase contrary to subclass 1 which decreased after reaching maintenance dose. No unambiguous relation between either the absolute value or the change of IgG1 and IgG4 at the time of challenge was observed in the patients who tolerated a sting. Furthermore, the IgG response was not correlated to the cumulative dose of venom administered. No simple regulatory function of IgG subclasses in the skin and IgE response was found, and the occurrence of local side effects did not seem to be determined by IgG antibodies. We conclude that clustered immunotherapy with Yellow Jacket venom is highly effective and that the frequency of side effects is acceptable.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

为评估临床疗效、副作用、体内和体外参数的差异,对25例对黄蜂过敏的患者采用分组免疫疗法进行治疗,每组之间的间隔为7天或14天。21例患者完成了6个月的治疗期,4例因不良反应(2例过敏性休克)退出。16例患者在医院内接受蜇刺激发试验,临床疗效良好。大多数患者观察到局部副作用,但很少限制免疫治疗的进程。通过皮内试验,以引起风团的毒液浓度估计皮肤敏感性,相当于0.1mg/ml盐酸组胺,治疗6个月后显著降低。特异性IgE最初升高,此后降至治疗前水平。通过三抗体测定法测定IgG亚类。仅亚类1和4显示有反应。亚类4呈稳定升高,与亚类1相反,亚类1在达到维持剂量后下降。在耐受蜇刺的患者中,未观察到激发时IgG1和IgG4的绝对值或变化之间存在明确关系。此外,IgG反应与给予的毒液累积剂量无关。未发现IgG亚类在皮肤和IgE反应中有简单的调节功能,局部副作用的发生似乎也不由IgG抗体决定。我们得出结论,黄蜂毒液分组免疫疗法非常有效,副作用发生率可以接受。(摘要截断于250字)

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