Vervloet D, Arnaud A, Senft M, Dor P, Bongrand P, Charpin J, Alazia M
J Allergy Clin Immunol. 1985 Mar;75(3):338-42. doi: 10.1016/0091-6749(85)90069-7.
In an earlier study we confirmed the usefulness of intradermal skin tests and histamine release in diagnosis of patients reactive to muscle relaxants, and we suggested an IgE-mediated reaction rather than an idiosyncratic mechanism. In a later study, we studied the relationship between (Formula: see text) that is one of the muscle relaxants producing the most frequent adverse reactions under anesthesia. Histamine release was measured in five patients with increasing concentrations of suxamethonium in the presence or absence of human serum albumin in Tris buffer. Suxamethonium by itself without any carrier in the buffer could, in vitro, act as a true allergen on target leukocytes in the sensitized patients' group. Acetylcholine (20 and 200 micrograms/ml) did not induce significant histamine release in five patients with positive histamine release in the presence of suxamethonium. Preincubation of leukocytes from 11 patients for 30 min with 20 and 200 micrograms of acetylcholine in Tris albumin CA++ Mg++ buffer decreased the histamine release induced by suxamethonium (10 micrograms/ml); mean maximal histamine release of 46% +/- 4.2 was reduced to 31.4 +/- 5.8 and 7% +/- 4 (p less than 0.001), respectively. However, in eight control subjects similar concentrations of acetylcholine did not change the maximal histamine release induced by anti-IgE (0.2 micrograms/ml). In the same way acetylcholine did not modify histamine release induced by Dermatophagoides pteronyssinus extract (1/10,000 w/v) in six patients allergic to this allergen. This study suggests that suxamethonium acts as a true allergen and that acetylcholine or one of its metabolites may act as a hapten inhibitor in the model of histamine release induced by suxamethonium.(ABSTRACT TRUNCATED AT 250 WORDS)
在一项早期研究中,我们证实了皮内皮肤试验和组胺释放对于诊断对肌肉松弛剂有反应的患者的有用性,并且我们提出这是一种由IgE介导的反应而非特异反应机制。在随后的一项研究中,我们研究了琥珀胆碱(在麻醉状态下引起最常见不良反应的肌肉松弛剂之一)与……之间的关系。在Tris缓冲液中,对5名患者在有或无人类血清白蛋白存在的情况下,随着琥珀胆碱浓度增加测量组胺释放。在缓冲液中无任何载体的琥珀胆碱自身,在体外可对致敏患者组的靶白细胞起到真正过敏原的作用。在琥珀胆碱存在时组胺释放呈阳性的5名患者中,乙酰胆碱(20和200微克/毫升)未诱导出显著的组胺释放。在Tris白蛋白Ca++Mg++缓冲液中,将11名患者的白细胞与20和200微克乙酰胆碱预孵育30分钟,可降低琥珀胆碱(10微克/毫升)诱导的组胺释放;平均最大组胺释放量从46%±4.2分别降至31.4±5.8和7%±4(p<0.001)。然而,在8名对照受试者中,类似浓度的乙酰胆碱并未改变抗IgE(0.2微克/毫升)诱导的最大组胺释放。同样,乙酰胆碱也未改变6名对该变应原过敏的患者中由屋尘螨提取物(1/10,000重量/体积)诱导的组胺释放。这项研究表明,琥珀胆碱起到真正过敏原的作用,并且乙酰胆碱或其代谢产物之一可能在琥珀胆碱诱导的组胺释放模型中作为半抗原抑制剂。(摘要截短至250字)