Adamek-Guzik T
II Katedry Chorób Wewnetrznych, Collegium Medicum Uniwersytetu, Jagiellońskiego, Krakowie.
Przegl Lek. 1994;51(4):161-6.
Clinical study was conducted on 77 adult patients with hypersensitivity to honey bee venom (HBV) to determine clinical characteristics and pathogenesis of hypersensitivity to HBV as well as the effect of specific immunotherapy(ITS) with HBV on several clinical and immunological parameters. The patients studied (43 women and 34 men of age ranging between 18-61 years with a mean age at 30 years) were divided into two groups: Group 1-44 patients with a history of anaphylactic shock following honey bee sting, who received specific immunotherapy with HBV. Group 2-33 patients hypersensitive to HBV(9 people reacted with severe anaphylactic systemic reaction, while others had skin reactions) who were not treated by ITS method. In all patients skin tests with HBV allergen were conducted before and at various stages of immunotherapy. Specific IgE (I1), s-IgG4 (I1), total IgE, IgG, IgA, IgM, C3c, C4 were estimated in sera samples obtained at the beginning, during the course and at the end of ITS. Dynamics of changes of these parameters were studied during a 3-year period of ITS. The challenge tests were conducted at the end of the treatment. 86.9% of treated patients reacted with IgE-mediated reactions. They showed elevated levels of s-IgE before immunotherapy, and significant decrease in s-IgE and increase in s-IgG4 titers after ITS. 10.4% of patients showed clinical symptoms of anaphylaxis, but non-IgE mediated. IgE titer in these patients was < or = 0.2 IU/ml and has not significantly changed during immunotherapy. s-IgG, levels were in these patients below 2 micrograms/ml.(ABSTRACT TRUNCATED AT 250 WORDS)
对77例对蜂毒(HBV)过敏的成年患者进行了临床研究,以确定HBV过敏的临床特征、发病机制以及HBV特异性免疫疗法(ITS)对若干临床和免疫参数的影响。所研究的患者(43名女性和34名男性,年龄在18至61岁之间,平均年龄30岁)分为两组:第1组-44例有蜂蛰后过敏性休克病史的患者,接受HBV特异性免疫疗法;第2组-33例对HBV过敏的患者(9人有严重的全身性过敏反应,其他人有皮肤反应),未采用ITS方法治疗。在所有患者中,在免疫疗法之前和各个阶段都进行了HBV过敏原皮肤试验。在ITS开始时、过程中及结束时采集的血清样本中检测特异性IgE(I1)、s-IgG4(I1)、总IgE、IgG、IgA、IgM、C3c、C4。在ITS的3年期间研究了这些参数的变化动态。在治疗结束时进行激发试验。86.9%的接受治疗的患者出现IgE介导的反应。他们在免疫疗法前s-IgE水平升高,ITS后s-IgE显著降低,s-IgG4滴度升高。10.4%的患者出现过敏反应的临床症状,但非IgE介导。这些患者的IgE滴度≤0.2 IU/ml,在免疫疗法期间没有显著变化。这些患者的s-IgG水平低于2微克/毫升。(摘要截短于250字)