Clark A T, Islam S, King Y, Deighton J, Anagnostou K, Ewan P W
Department of Allergy, Cambridge University Hospitals NHS Foundation Trust, Box 40, Addenbrooke's Hospital, Hills Roads, Cambridge CB2 2QQ, UK.
Allergy. 2009 Aug;64(8):1218-20. doi: 10.1111/j.1398-9995.2009.01982.x. Epub 2009 Feb 17.
Peanut allergy is common, potentially severe and rarely resolves causing impaired quality of life. No disease-modifying treatment exists and there is therefore a need to develop a therapeutic intervention.
The aim of this study was to investigate whether peanut oral immunotherapy (OIT) can induce clinical tolerance to peanut protein.
Four peanut-allergic children underwent OIT. Preintervention oral challenges were performed to confirm clinical allergy and define the amount of protein required to cause a reaction (dose thresholds). OIT was then administered as daily doses of peanut flour increasing from 5 to 800 mg of protein with 2-weekly dose increases. After 6 further weeks of treatment, the oral challenge was repeated to define change in dose threshold and subjects continued daily treatment.
Preintervention challenges confirmed peanut allergy and revealed dose thresholds of 5-50 mg (1/40-1/4 of a whole peanut); one subject had anaphylaxis during challenge and required adrenaline injection. All subjects tolerated immunotherapy updosing to 800 mg protein and i.m. adrenaline was not required. Each subject tolerated at least 10 whole peanuts (approximately 2.38 g protein) in postintervention challenges, an increase in dose threshold of at least 48-, 49-, 55- and 478-fold for the four subjects.
We demonstrated a substantial increase in dose threshold after OIT in all subjects, including the subject with proven anaphylaxis. OIT was well tolerated and conferred protection against at least 10 peanuts, more than is likely to be encountered during accidental ingestion.
花生过敏很常见,可能很严重,且很少缓解,会导致生活质量受损。目前尚无改善病情的治疗方法,因此需要开发一种治疗性干预措施。
本研究的目的是调查花生口服免疫疗法(OIT)是否能诱导对花生蛋白的临床耐受性。
四名花生过敏儿童接受了OIT。在干预前进行口服激发试验以确认临床过敏并确定引发反应所需的蛋白量(剂量阈值)。然后给予OIT,每日剂量为花生粉,从5毫克蛋白增加到800毫克蛋白,每两周增加一次剂量。在进一步治疗6周后,重复口服激发试验以确定剂量阈值的变化,受试者继续每日治疗。
干预前的激发试验证实了花生过敏,并揭示了5-50毫克(1/40-1/4颗完整花生)的剂量阈值;一名受试者在激发试验期间发生过敏反应,需要注射肾上腺素。所有受试者都耐受了高达800毫克蛋白的免疫疗法递增剂量,无需注射肾上腺素。在干预后的激发试验中,每个受试者至少耐受10颗完整花生(约2.38克蛋白),四名受试者的剂量阈值分别增加了至少48倍、49倍、55倍和478倍。
我们证明,在所有受试者中,包括已证实发生过敏反应的受试者,OIT后剂量阈值大幅提高。OIT耐受性良好,可提供针对至少10颗花生的保护,超过意外摄入时可能遇到的量。