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一项关于林克尔免疫疗法治疗豚草花粉性枯草热有效性的对照研究。

A controlled study of the effectiveness of the Rinkel method of immunotherapy for ragweed pollen hay fever.

作者信息

Van Metre T E, Adkinson N F, Lichtenstein L M, Mardiney M R, Norman P S, Rosenberg G L, Sobotka A K, Valentine M D

出版信息

J Allergy Clin Immunol. 1980 Apr;65(4):288-97. doi: 10.1016/0091-6749(80)90158-x.

Abstract

In a double-blind study, we compared the effects of the Rinkel method of immunotherapy with ragweed pollen extract and placebo on symptoms of ragweed hay fever and immunologic parameters in 24 ragweed-sensitive patients. Each had a skin-test end point by Rinkel serial dilution titration to ragweed pollen extract at 1:312,500 w/v or greater dilution, a 2 + skin test to ragweed AgE at 0.1 microgram /ml or greater dilution, and in vitro leukocyte histamine release by ragweed pollen extract. None had had immunotherapy for at least 7 yr. Patients matched on the basis of leukocyte histamine release by ragweed were assigned to two treatment groups (12 patients in each group). One group received ragweed pollen extract, and the other, placebo, both administered by the Rinkel method between June and October, 1978. Treatment doses were derived from skin-test end points. The median maintenance ("optimal dose") for patients receiving ragweed pollen extract was 0.53 ml of 1:312,500 w/v and the mean cumulative dose of ragweed pollen extract given during the study contained 0.094 micrograms of ragweed AgE. Symptom-medication scores of all patients rose and fell with ragweed pollen counts. No significant differences were observed in mean daily symptom-medication scores, antiragweed IgG or IgE levels, leukocyte histamine release by ragweed, total IgE levels, or skin-test end-point dilutions with ragweed pollen extract between the group receiving ragweed pollen extract and the group receiving placebo. Despite the absence of specific effect on symptom-medication scores and measured immunologic variates, 10 3f the 12 ragweed-treated patients and 10 of the 12 placebo-treated patients were of the opinion that their hay fever symptoms during the ragweed pollen season were less severe in 1978 than in 1977 and that they had been helped by Rinkel method immunotherapy. Under the conditions of the study, Rinkel method immunotherapy with ragweed pollen extract was no more effective than placebo given in an imitation of the Rinkel method.

摘要

在一项双盲研究中,我们比较了用豚草花粉提取物及安慰剂的林克尔免疫疗法对24例豚草敏感患者的豚草花粉热症状及免疫参数的影响。每位患者通过对豚草花粉提取物进行林克尔系列稀释滴定,在1:312,500 w/v或更高稀释度时达到皮肤试验终点,对0.1微克/毫升或更高稀释度的豚草变应原E进行2+皮肤试验,以及对豚草花粉提取物进行体外白细胞组胺释放试验。至少7年未进行过免疫疗法。根据豚草引起的白细胞组胺释放情况匹配的患者被分为两个治疗组(每组12例患者)。一组接受豚草花粉提取物,另一组接受安慰剂,二者均在1978年6月至10月期间采用林克尔方法给药。治疗剂量根据皮肤试验终点确定。接受豚草花粉提取物的患者的中位维持量(“最佳剂量”)为1:312,500 w/v的0.53毫升,研究期间给予的豚草花粉提取物的平均累积剂量含有0.094微克豚草变应原E。所有患者的症状-用药评分随豚草花粉计数而升降。在接受豚草花粉提取物的组和接受安慰剂的组之间,平均每日症状-用药评分、抗豚草IgG或IgE水平、豚草引起的白细胞组胺释放、总IgE水平或豚草花粉提取物的皮肤试验终点稀释度均未观察到显著差异。尽管对症状-用药评分和所测免疫变量没有特异性影响,但接受豚草治疗的12例患者中有10例,接受安慰剂治疗的12例患者中有10例认为他们在1978年豚草花粉季节的花粉热症状比1977年轻,并且林克尔方法免疫疗法对他们有帮助。在该研究条件下,用豚草花粉提取物进行林克尔方法免疫疗法并不比模仿林克尔方法给予的安慰剂更有效。

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