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在严重迟发性免疫介导的抗生素药物不良反应中体内和体外诊断工具的作用。

The Role of In Vivo and Ex Vivo Diagnostic Tools in Severe Delayed Immune-Mediated Adverse Antibiotic Drug Reactions.

机构信息

Centre for Antibiotic Allergy and Research, Department of Infectious Diseases, Austin Health, Heidelberg, VIC, Australia; Clinical Immunology and Allergy, McGill University Health Center, Montréal, QC, Canada.

Centre for Antibiotic Allergy and Research, Department of Infectious Diseases, Austin Health, Heidelberg, VIC, Australia.

出版信息

J Allergy Clin Immunol Pract. 2021 May;9(5):2010-2015.e4. doi: 10.1016/j.jaip.2020.12.052. Epub 2021 Jan 13.

Abstract

BACKGROUND

The use of in vivo and ex vivo diagnostic tools for delayed immune-mediated adverse drug reactions is currently ill defined.

OBJECTIVE

To determine whether the combination of skin testing and/or IFN-γ enzyme-linked immunoSpot assay (ELISpot) can aid diagnosis of these allergy phenotypes.

METHODS

Patients with antibiotic-associated severe delayed immune-mediated adverse drug reaction hypersensitivity, including Stevens-Johnson syndrome and toxic epidermal necrolysis, drug reaction with eosinophilia and systemic symptoms (DRESS), acute generalized exanthematous pustulosis, generalized bullous fixed drug eruption, and severe maculopapular exanthema, were prospectively recruited. In vivo testing was completed to the implicated drug(s), and ex vivo testing was performed with the patient's PBMCs stimulated with the relevant antibiotic concentrations for IFN-γ release ELISpot measurement.

RESULTS

Eighty-one patients met the inclusion criteria, with DRESS (42; 51.9%) accounting for most cases. Among the 63 (78%) who had an ELISpot assay performed, 34 (54%) were positive to at least 1 implicated antibiotic (median spot-forming units/million cells, 99.5; interquartile range, 68-187), with glycopeptide being a strong predictor of positivity (adjusted odds ratio, 6.11; 95% CI, 1.74-21.42). In combination (in vivo and ex vivo), 51 (63%) of those tested were positive to an implicated antibiotic. For DRESS and severe maculopapular exanthema associated with penicillins and cephalosporins, this combination confirmed the culprit agent in 11 of the 12 cases and in 6 of 7 for DRESS associated with glycopeptides.

CONCLUSIONS

This study demonstrates that using in vivo in combination with ex vivo testing can enhance the diagnostic approach in these severe phenotypes by assisting with the identification of possible culprit antibiotics.

摘要

背景

目前,用于诊断迟发性免疫介导的药物不良反应的体内和体外诊断工具的使用尚未明确。

目的

确定皮肤试验和/或干扰素-γ酶联免疫斑点(ELISpot)检测是否有助于诊断这些过敏表型。

方法

前瞻性招募了抗生素相关性严重迟发性免疫介导的药物不良反应过敏反应患者,包括史蒂文斯-约翰逊综合征和中毒性表皮坏死松解症、药物反应伴嗜酸性粒细胞增多和全身症状(DRESS)、急性泛发性发疹性脓疱病、全身性大疱性固定性药疹和严重斑丘疹性发疹。对可疑药物进行了体内检测,并使用患者的 PBMC 与相关抗生素浓度刺激进行了体外检测,以进行干扰素-γ释放 ELISpot 测量。

结果

符合纳入标准的 81 例患者中,DRESS(42 例;51.9%)占大多数。在进行 ELISpot 检测的 63 例(78%)患者中,至少有 1 种可疑抗生素阳性(中位斑点形成单位/百万细胞,99.5;四分位间距,68-187),糖肽是阳性的强烈预测因素(调整优势比,6.11;95%CI,1.74-21.42)。在联合(体内和体外)检测中,51 例(63%)测试患者对可疑抗生素呈阳性。对于与青霉素和头孢菌素相关的 DRESS 和严重斑丘疹性发疹,该组合在 12 例中的 11 例和与糖肽相关的 DRESS 的 7 例中的 6 例中确认了罪魁祸首药物。

结论

这项研究表明,在这些严重表型中,结合体内和体外检测可以增强诊断方法,有助于确定可能的罪魁祸首抗生素。

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