Intérêt d’un nouveau protocole de cytomètrie en flux appliqué au diagnostic et à la prévention des accidents peranesthésiques aux curares

J. Sainte-Laudy , I. Orsel
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引用次数: 3

Abstract

Aim of the study

We tested here a new cytometric method based on the use of two activation markers (CD63 and IgE) and result's expression in activation index (AI).

Material and methods

Twenty-six allergic patients and 23 controls having received a neuromuscular blocker (NMB) have been selected on the basis of clinical history, skin tests and specific IgEs. NMB were tested mixed (n = 26) or alone (injectable form, (n = 30) and allergens commercialized for flow cytometry (n = 9)). Concentrations used were the same than for IDR according to the recommandations of the French Society of Anaesthesia and Resuscitation (SFAR). The cytometric protocol used was the IgE/CD63 protocol, results being expressed in percentage CD63 and in AI calculated by a specific algorithm involving the mean fluorescence intensity (MFI) of the IgE+ and the CD63+ and − populations.

Results

In the technical described here NMB exhibited no toxicity even for concentretions 10 times higher than concentrations used for diagnosis. With the injectable form, the respective sensitivities observed for CD63 alone and the AI were 68 and 100% for the mixture of NMB and, 67 and 100% for the isolated NMB. With the NMB commercialized for flow cytometry, sensitivities were 47 and 100%. Specificities were 100% for CD63 alone and 98% for the AI. The link (Chi2) between skin tests and flow cytometry was significant for the two markers and the two allergen types. Correlation between AI and specific IgEs was not significant.

Conclusion

The new flow cytometric protocol described here has the necessary characteristics of a biological test which could be included in the pre-anaesthetic check up.

一种新的流式细胞术方案应用于curares麻醉期事故的诊断和预防的兴趣
研究目的:利用CD63和IgE两种激活标记物及其在激活指数(AI)中的表达,研究了一种新的细胞检测方法。材料与方法根据临床病史、皮肤试验和特异性IgEs,选择26例接受神经肌肉阻滞剂(NMB)治疗的过敏患者和23例对照组。NMB混合(n = 26)或单独(注射形式,n = 30)和商业化用于流式细胞术的过敏原(n = 9)进行测试。根据法国麻醉与复苏学会(SFAR)的建议,使用的浓度与IDR相同。使用的细胞分析方案是IgE/CD63方案,结果以CD63百分比表示,并通过涉及IgE+和CD63+和-群体的平均荧光强度(MFI)的特定算法计算AI。结果在本技术中,即使NMB的浓度比诊断浓度高10倍,也没有毒性。在注射形式下,单独CD63和AI对NMB混合物的敏感性分别为68%和100%,对分离NMB的敏感性分别为67%和100%。随着NMB商业化用于流式细胞术,灵敏度分别为47%和100%。CD63特异性为100%,AI特异性为98%。对于两种标记物和两种过敏原类型,皮肤试验和流式细胞术之间的联系(Chi2)是显著的。AI与特异性IgEs的相关性不显著。结论新的流式细胞术方案具有生物学检查的必要特征,可纳入麻醉前检查。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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