Settipane R A, Stevenson D D
Scripps Clinic and Research Foundation, La Jolla, Calif. 92037.
J Allergy Clin Immunol. 1989 Jul;84(1):26-33. doi: 10.1016/0091-6749(89)90174-7.
Drugs inhibiting cyclooxygenase regularly cross-react with aspirin (ASA). Although some experiments suggest that acetaminophen (ACETM) is a weak inhibitor of cyclooxygenase in certain tissues, it has not been studied in human lung tissue, and controversy exists whether or not true cross-reactivity occurs between ASA and ACETM. Three ASA-sensitive subjects with asthma, who gave a history of reactions to ACETM, underwent double-blind, placebo-controlled challenges and reacted to 1000 mg of ACETM with a greater than 20% fall in FEV1. Two patients were desensitized to ASA and then were rechallenged with 1000 mg of ACETM without reaction. Two patients were desensitized to increasing doses of ACETM, achieving refractoriness to 1500 mg, but not 2000 mg. Thus, cross sensitivity between ASA and ACETM was documented when large challenge doses (1000 mg) of ACETM were used. Furthermore, cross desensitization suggests that in ASA-sensitive subjects with asthma, similar mechanisms are likely to be responsible for reactions to ASA, nonsteroidal anti-inflammatory drugs, and ACETM.
抑制环氧化酶的药物经常与阿司匹林(ASA)发生交叉反应。尽管一些实验表明对乙酰氨基酚(ACETM)在某些组织中是环氧化酶的弱抑制剂,但尚未在人肺组织中进行研究,并且关于ASA和ACETM之间是否真的发生交叉反应存在争议。三名有哮喘且对ACETM有反应史的ASA敏感受试者接受了双盲、安慰剂对照激发试验,对1000mg的ACETM产生反应,FEV1下降超过20%。两名患者对ASA进行了脱敏,然后用1000mg的ACETM再次激发试验,未出现反应。两名患者对递增剂量的ACETM进行了脱敏,对1500mg产生耐受,但对2000mg不耐受。因此,当使用大剂量(1000mg)的ACETM进行激发试验时,记录到了ASA和ACETM之间的交叉敏感性。此外,交叉脱敏表明,在有哮喘的ASA敏感受试者中,对ASA、非甾体抗炎药和ACETM的反应可能由相似的机制引起。