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分子诊断与免疫疗法。

Molecular diagnosis and immunotherapy.

作者信息

Sastre Joaquín, Sastre-Ibañez Marina

机构信息

aAllergy Department Fundación Jiménez Díaz and CIBER de Enfermedades Respiratorias (CIBERES, Institute Carlos III, Ministry of Economy and Competitiveness) bHospital Clínico San Carlos, Madrid, Spain.

出版信息

Curr Opin Allergy Clin Immunol. 2016 Dec;16(6):565-570. doi: 10.1097/ACI.0000000000000318.

Abstract

PURPOSE OF REVIEW

To describe recent insights into how molecular diagnosis can improve indication and selection of suitable allergens for specific immunotherapy and increase the safety of this therapy.

RECENT FINDINGS

As specific allergen immunotherapy targets specific allergens, identification of the disease-eliciting allergen is a prerequisite for accurate prescription of treatment. In areas of complex sensitization to aeroallergens or in cases of hymenoptera venom allergy, the use of molecular diagnosis has demonstrated that it may lead to a change in indication and selection of allergens for immunotherapy in a large proportion of patients when compared with diagnosis based on skin prick testing and/or specific IgE determination with commercial extracts. These changes in immunotherapy prescription aided by molecular diagnosis have been demonstrated to be cost-effective in some scenarios. Certain patterns of sensitization to grass or olive pollen and bee allergens may identify patients with higher risk of adverse reaction during immunotherapy.

SUMMARY

Molecular diagnosis, when used with other tools and patients' clinical records, can help clinicians better to select the most appropriate patients and allergens for specific immunotherapy and, in some cases, predict the risk of adverse reactions. The pattern of sensitization to allergens could potentially predict the efficacy of allergen immunotherapy provided that these immunotherapy products contain a sufficient amount of these allergens. Nevertheless, multiplex assay remains a third-level approach, not to be used as screening method in current practice.

摘要

综述目的

描述近期关于分子诊断如何改善特异性免疫治疗中合适变应原的适应症及选择并提高该治疗安全性的见解。

近期发现

由于特异性变应原免疫治疗针对特定变应原,确定引发疾病的变应原是准确开具治疗处方的前提。在对气传变应原复杂致敏的区域或膜翅目毒液过敏的病例中,与基于皮肤点刺试验和/或使用商业提取物测定特异性IgE的诊断相比,分子诊断已证明在很大一部分患者中可能会导致免疫治疗变应原的适应症和选择发生变化。在某些情况下,分子诊断辅助的免疫治疗处方变化已被证明具有成本效益。对草或橄榄花粉以及蜜蜂变应原的某些致敏模式可能识别出免疫治疗期间发生不良反应风险较高的患者。

总结

分子诊断与其他工具和患者临床记录一起使用时,可帮助临床医生更好地为特异性免疫治疗选择最合适的患者和变应原,并且在某些情况下预测不良反应风险。如果这些免疫治疗产品含有足够量的变应原,变应原致敏模式可能潜在地预测变应原免疫治疗的疗效。然而,多重检测仍然是一种三级方法,在当前实践中不作为筛查方法使用。

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