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昆虫过敏诊断评估的新方向。

New directions in diagnostic evaluation of insect allergy.

作者信息

Golden David B K

机构信息

Johns Hopkins University, Baltimore, Maryland, USA.

出版信息

Curr Opin Allergy Clin Immunol. 2014 Aug;14(4):334-9. doi: 10.1097/ACI.0000000000000072.

Abstract

PURPOSE OF REVIEW

Diagnosis of insect sting allergy and prediction of risk of sting anaphylaxis are often difficult because tests for venom-specific IgE antibodies have a limited positive predictive value and do not reliably predict the severity of sting reactions.

RECENT FINDINGS

Component-resolved diagnosis using recombinant venom allergens has shown promise in improving the specificity of diagnostic testing for insect sting allergy. Basophil activation tests have been explored as more sensitive assays for identification of patients with insect allergy and for prediction of clinical outcomes. Measurement of mast cell mediators reflects the underlying risk for more severe reactions and limited clinical response to treatment.

SUMMARY

Measurement of IgE to recombinant venom allergens can distinguish cross-sensitization from dual sensitization to honeybee and vespid venoms, thus helping to limit venom immunotherapy to a single venom instead of multiple venoms in many patients. Basophil activation tests can detect venom allergy in patients who show no detectable venom-specific IgE in standard diagnostic tests and can predict increased risk of systemic reactions to venom immunotherapy, and to stings during and after stopping venom immunotherapy. The risk of severe or fatal anaphylaxis to stings can also be predicted by measurement of baseline serum tryptase or other mast cell mediators.

摘要

综述目的

昆虫叮咬过敏的诊断以及叮咬过敏反应风险的预测往往存在困难,因为针对毒液特异性IgE抗体的检测阳性预测值有限,且无法可靠地预测叮咬反应的严重程度。

最新发现

使用重组毒液变应原进行组分解析诊断在提高昆虫叮咬过敏诊断检测的特异性方面显示出前景。嗜碱性粒细胞活化试验已被探索作为一种更敏感的检测方法,用于识别昆虫过敏患者以及预测临床结果。肥大细胞介质的测量反映了更严重反应和治疗临床反应有限的潜在风险。

总结

检测针对重组毒液变应原的IgE可以区分对蜜蜂和黄蜂毒液的交叉致敏与双重致敏,从而有助于在许多患者中将毒液免疫疗法限制于单一毒液而非多种毒液。嗜碱性粒细胞活化试验可以在标准诊断检测中未检测到毒液特异性IgE的患者中检测到毒液过敏,并可以预测毒液免疫疗法期间以及停止毒液免疫疗法期间及之后叮咬引起的全身反应风险增加。通过测量基线血清类胰蛋白酶或其他肥大细胞介质也可以预测叮咬导致严重或致命过敏反应的风险。

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