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肌肉松弛剂过敏反应:通过放射免疫测定法与皮内试验对34例病例的交叉敏感性进行研究。

Anaphylaxis to muscle relaxants: cross-sensitivity studied by radioimmunoassays compared to intradermal tests in 34 cases.

作者信息

Moneret-Vautrin D A, Guéant J L, Kamel L, Laxenaire M C, el Kholty S, Nicolas J P

机构信息

Service d'Immuno-Allergologie, Faculté de Médecine, Nancy, France.

出版信息

J Allergy Clin Immunol. 1988 Nov;82(5 Pt 1):745-52. doi: 10.1016/0091-6749(88)90074-7.

Abstract

Thirty-four patients (31 female and three male patients) with a previous anaphylactoid shock to muscle relaxants were investigated. The seric antimyorelaxant IgE was detected by radioimmunoassay (RIA), and the results were compared to intradermal test (IDR) reactions to dilutions of the commercial drugs. The RIA was carried out with a Sepharose-myorelaxant solid phase and anti-IgE 125I-labeled IgG. The results corresponded to the percentage of labeled anti-IgE bound on the solid phase. The RIA with Sepharose-alcuronium and Sepharose-choline was estimated positive from determination with normal sera (n = 12) when bound IgE was greater than 1.0% and 1.5%, respectively. The RIA and IDR were positive in 43.5% and 75%, respectively, of the cases, with a concordance of 66%. One test at least was positive in 79.4% of the cases. No correlation was found between IgE seric levels and the RIA nor between the cutaneous sensitivity and the RIA. Cross-reactivity with Sepharose-choline and Sepharose-alcuronium was observed in 50%, and it was demonstrated by IDR in only 34.2%. The RIA demonstrated the specificity of IgE to quaternary ammonium compounds as myorelaxant drugs. The positive IDR revealed the bridging of mast cell-bound specific IgE, depending on structural conditions, such as the flexibility of the molecules or the variable specificity of the antibodies, restricted to quaternary ammonium ions or enlarged to a broader part of the incriminated molecules.

摘要

对34例曾对肌肉松弛剂发生类过敏反应的患者(31例女性和3例男性患者)进行了研究。通过放射免疫测定法(RIA)检测血清抗肌肉松弛剂IgE,并将结果与对市售药物稀释液的皮内试验(IDR)反应进行比较。使用琼脂糖 - 肌肉松弛剂固相和抗IgE 125I标记的IgG进行RIA。结果对应于固相上结合的标记抗IgE的百分比。当结合的IgE分别大于1.0%和1.5%时,用正常血清(n = 12)测定,琼脂糖 - 阿库氯铵和琼脂糖 - 胆碱的RIA估计为阳性。RIA和IDR分别在43.5%和75%的病例中呈阳性,一致性为66%。79.4%的病例中至少有一项试验呈阳性。未发现IgE血清水平与RIA之间以及皮肤敏感性与RIA之间存在相关性。50%的病例观察到与琼脂糖 - 胆碱和琼脂糖 - 阿库氯铵的交叉反应性,而皮内试验仅在34.2%的病例中证实了这种交叉反应性。RIA证明了IgE对作为肌肉松弛剂药物的季铵化合物的特异性。阳性皮内试验揭示了肥大细胞结合的特异性IgE的桥接,这取决于结构条件,如分子的柔韧性或抗体的可变特异性,限于季铵离子或扩大到涉案分子的更广泛部分。

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