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人类过敏性哮喘中节段性变应原激发试验的安全性

Safety of segmental allergen challenge in human allergic asthma.

作者信息

Julius Peter, Lommatzsch Marek, Kuepper Michael, Bratke Kai, Faehndrich Sebastian, Luttmann Werner, Virchow Johann Christian

机构信息

Department of Pneumology, University of Rostock, Rostock, Germany.

出版信息

J Allergy Clin Immunol. 2008 Mar;121(3):712-7. doi: 10.1016/j.jaci.2007.08.058. Epub 2007 Oct 29.

Abstract

BACKGROUND

Segmental allergen challenge is widely used to study mechanisms of human allergic asthma. Despite the relatively large dissemination, limited information is available about the safety of this method.

OBJECTIVE

Observational, retrospective study to report the adverse events of segmental allergen challenge in a large group of volunteers with asthma.

METHODS

In total, 78 cases from several studies performed between 1994 and 2007 were pooled for this analysis. Volunteers underwent allergen challenge using either a fixed dose of allergen (7 cases) or an individually standardized allergen dose defined by an inhaled allergen test before the challenge (71 cases). A subgroup of 13 volunteers underwent repeated challenges, with more than 6 months between the challenges.

RESULTS

With a fixed dose instilled during bronchoscopy, 43% of the participants developed wheezing and coughing, requiring 2-6 puffs of a ss(2)-agonist after segmental allergen challenge. In volunteers with individually standardized doses, a ss(2)-agonist was required in only 19% of the cases. No severe adverse events occurred in all cases studied. Volunteers who underwent repeated challenges did not develop more adverse events than those who underwent 1 challenge.

CONCLUSIONS

Segmental allergen challenge is a safe tool to study the mechanisms of human allergic asthma, even when repeated challenges are performed in the same patient. It is associated with only a few, tolerable adverse events, especially when the dose of allergen is standardized individually.

摘要

背景

节段性变应原激发试验广泛用于研究人类过敏性哮喘的机制。尽管该方法应用较为广泛,但关于其安全性的信息有限。

目的

进行观察性回顾性研究,报告一大组哮喘志愿者节段性变应原激发试验的不良事件。

方法

汇总了1994年至2007年间几项研究中的78例病例进行分析。志愿者采用固定剂量变应原(7例)或在激发试验前通过吸入变应原试验确定的个体标准化变应原剂量进行变应原激发试验(71例)。13名志愿者的亚组进行了重复激发试验,两次激发试验间隔超过6个月。

结果

在支气管镜检查期间注入固定剂量变应原时,43%的参与者出现喘息和咳嗽,节段性变应原激发试验后需要吸入2 - 6喷短效β₂激动剂。在使用个体标准化剂量的志愿者中,仅19%的病例需要吸入短效β₂激动剂。所有研究病例均未发生严重不良事件。进行重复激发试验的志愿者与进行1次激发试验的志愿者相比,并未出现更多不良事件。

结论

节段性变应原激发试验是研究人类过敏性哮喘机制的安全工具,即使在同一患者中进行重复激发试验也是如此。它仅伴有少数可耐受的不良事件,尤其是当变应原剂量进行个体标准化时。

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