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草花粉过敏患者舌下免疫疗法与注射免疫疗法的双盲(双模拟)研究

Sublingual versus injective immunotherapy in grass pollen allergic patients: a double blind (double dummy) study.

作者信息

Quirino T, Iemoli E, Siciliani E, Parmiani S, Milazzo F

机构信息

Servizio di Allergologia Ospedale L. Sacco, Milan, Italy.

出版信息

Clin Exp Allergy. 1996 Nov;26(11):1253-61.

PMID:8955574
Abstract

BACKGROUND

Injective immunotherapy is a well-known and recognized treatment for allergic diseases, but its safety has been questioned during recent years. Alternative administration routes have been proposed and there is a growing interest and experience in sublingual therapy. The safety of alternative routes is nonetheless a real advantage, so long as it is not counterbalanced by a loss of clinical benefit.

OBJECTIVE

We have compared the efficacy of the same biologically standardized grass pollen extract administered through the injective or the sublingual route, in a group of 20 patients followed for two pollen seasons.

METHODS

Both therapies were administered for 12 months according to a double-blind (double-dummy) plan; at the end of the trial the cumulative dosage of the sublingual therapy was 2.4 times higher than that of the injective therapy. Data about skin reactivity, symptoms and drugs scores during the pollen season, as well as total specific IgG and specific IgG4, during and after the trial, were obtained.

RESULTS

Our data show that sublingual and injective therapy are equally effective according to subjective clinical parameters, with a statistically highly significant reduction of symptoms and drugs (P = 0.002 for symptoms and drugs in SLIT-treated patients; P = 0.002 for symptoms and P = 0.0039 for drugs in patients given injections). On the other hand, objective parameters (total specific IgG, specific IgG4, skin reactivity) changed only in patients treated with active injective therapy, with P < 0.001, P < 0.001 and P = 0.021, respectively.

CONCLUSIONS

The discrepancies observed could be interpreted as a consequence of different mechanisms of actin of the two therapies or to the lack of close relationships between the clinical and the objective parameters which were considered here.

摘要

背景

注射免疫疗法是一种治疗过敏性疾病的知名且公认的方法,但近年来其安全性受到质疑。已提出替代给药途径,舌下疗法的关注度和经验也在不断增加。只要不会因临床疗效降低而抵消其优势,替代途径的安全性就是一项实实在在的优势。

目的

我们比较了通过注射或舌下途径给予同一生物标准化草花粉提取物的疗效,对20名患者进行了两个花粉季节的随访。

方法

两种疗法均按照双盲(双模拟)方案给药12个月;试验结束时,舌下疗法的累积剂量比注射疗法高2.4倍。获取了花粉季节期间的皮肤反应性、症状和药物评分数据,以及试验期间和试验后的总特异性IgG和特异性IgG4数据。

结果

我们的数据表明,根据主观临床参数,舌下疗法和注射疗法同样有效,症状和药物使用量均有统计学上的显著降低(舌下免疫疗法治疗的患者症状和药物使用量P = 0.002;注射治疗的患者症状P = 0.002,药物使用量P = 0.0039)。另一方面,客观参数(总特异性IgG、特异性IgG4、皮肤反应性)仅在接受活性注射疗法的患者中发生变化,P值分别<0.001、<0.001和 = 0.021。

结论

观察到的差异可以解释为两种疗法作用机制不同的结果,或者是此处所考虑的临床参数与客观参数之间缺乏紧密关联的结果。

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