Passalacqua Giovanni, Guerra Laura, Compalati Enrico, Canonica Giorgio Walter
Allergy and Respiratory Diseases, Department of Internal Medicine, University of Genoa, Genoa, Italy.
Curr Drug Saf. 2007 May;2(2):117-23. doi: 10.2174/157488607780598340.
Sublingual immunotherapy (SLIT) was proposed for clinical practice about 20 years ago with the main aim of improving the safety and of avoiding the side effects. More than 30 randomized controlled trials have been published so far, in addition to several post marketing surveys. Thus, the literature provides a solid documentation of the safety profile of this treatment. Concerning the randomized controlled trials, the more frequently reported side effect of SLIT is the oral itching or swelling, followed by gastrointestinal complaints. These side effects are invariantly described as mild and easily managed by temporarily adjusting the dose. Systemic relevant adverse events (asthma, urticaria, angioedema) occur sporadically, with their rate not being different from the placebo groups. Moreover, the safety profile seems not to differ in adults and children. More interestingly, the post marketing surveys consistently showed that the occurrence of all side effects is less than 20% of patients and less than 1 per 1,000 doses, thus being quite insignificant compared to subcutaneous immunotherapy. The most recent surveys showed that the rate of adverse events does not increase in children below the age of 5 years, being traditionally considered as a prudential limit for injection IT. Finally, it seems that the occurrence of some adverse events, at variance with injection route, does not depend strictly on the dose of allergen administered.
大约20年前,舌下免疫疗法(SLIT)被应用于临床实践,其主要目的是提高安全性并避免副作用。到目前为止,除了几项上市后调查外,已经发表了30多项随机对照试验。因此,文献为该治疗方法的安全性提供了确凿的记录。关于随机对照试验,SLIT最常报告的副作用是口腔瘙痒或肿胀,其次是胃肠道不适。这些副作用无一例外地被描述为轻微的,通过暂时调整剂量很容易控制。全身性相关不良事件(哮喘、荨麻疹、血管性水肿)偶尔发生,其发生率与安慰剂组没有差异。此外,成人和儿童的安全性似乎没有差异。更有趣的是,上市后调查一致显示,所有副作用的发生率在患者中不到20%,每1000剂中不到1例,因此与皮下免疫疗法相比相当微不足道。最近的调查显示,5岁以下儿童的不良事件发生率并未增加,传统上认为这是注射免疫疗法的谨慎界限。最后,与注射途径不同,一些不良事件的发生似乎并不严格取决于所给予的变应原剂量。