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欧洲过敏与临床免疫学会变应原特异性免疫治疗剂量-反应关系工作组报告

European Academy of Allergy and Clinical Immunology task force report on 'dose-response relationship in allergen-specific immunotherapy'.

机构信息

National Heart and Lung Institute, Imperial College London, UK.

出版信息

Allergy. 2011 Oct;66(10):1345-59. doi: 10.1111/j.1398-9995.2011.02669.x. Epub 2011 Jun 28.

Abstract

BACKGROUND

For a century, allergen-specific immunotherapy (SIT) has proven to be an effective treatment for allergic rhinitis, asthma, and insect sting allergy. However, as allergen doses are frequently adapted to the individual patient, there are few data on dose-response relationship in SIT. Allergen products for SIT are being increasingly required to conform to regulatory requirements for human medicines, which include the need to demonstrate dose-dependent effects.

METHODS

This report, produced by a Task Force of the EAACI Immunotherapy Interest Group, evaluates the currently available data on dose-response relationships in SIT and aims to provide recommendations for the design of future studies.

RESULTS

Fifteen dose-ranging studies fulfilled the inclusion criteria and twelve reported a dose-response relationship for clinical efficacy. Several studies also reported a dose-response relationship for immunological and safety endpoints. Due to the use of different reference materials and methodologies for the determination of allergen content, variations in study design, and choice of endpoints, no comparisons could be made between studies and, as a consequence, no general dosing recommendations can be made.

CONCLUSION

Despite recently introduced guidelines on the standardization of allergen preparations and study design, the Task Force identified a need for universally accepted standards for the measurement of allergen content in SIT preparations, dosing protocols, and selection of clinical endpoints to enable dose-response effects to be compared across studies.

摘要

背景

一个世纪以来,过敏原特异性免疫治疗(SIT)已被证明是治疗过敏性鼻炎、哮喘和昆虫叮咬过敏的有效方法。然而,由于过敏原剂量经常根据个体患者进行调整,因此关于 SIT 中剂量-反应关系的数据很少。用于 SIT 的过敏原产品越来越需要符合人类药物的监管要求,其中包括需要证明剂量依赖性效应。

方法

本报告由 EAACI 免疫治疗兴趣小组的一个工作组编写,评估了 SIT 中目前可获得的剂量-反应关系数据,并旨在为未来研究的设计提供建议。

结果

符合纳入标准的有 15 项剂量范围研究,并报告了 12 项临床疗效的剂量-反应关系。一些研究还报告了免疫学和安全性终点的剂量-反应关系。由于过敏原含量测定的参考物质和方法不同、研究设计和终点选择的差异,因此无法对研究进行比较,因此无法提出一般的剂量建议。

结论

尽管最近出台了过敏原制剂和研究设计标准化指南,但工作组仍发现需要普遍接受的 SIT 制剂过敏原含量、剂量方案和临床终点选择的测量标准,以能够比较研究之间的剂量反应效应。

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