Allergy Asthma Proc. 2022 Jul 1;43(4):254-259. doi: 10.2500/aap.2022.43.220030.
There are currently no biomarkers that can accurately predict clinical outcomes and segregate responders from nonresponders in allergen immunotherapy (AIT). Therefore, identifying a reliable predictive biomarker is essential to enable clinicians to tailor personalized therapy. New developments in AIT biomarkers are currently being explored, and it would be important to identify key areas of development and their feasibility for use in the clinic. Biomarkers can be categorized broadly into seven domains: (i) Immunoglobulin E (IgE), (ii) IgG and IgA responses, (iii) IgE -facilitated allergen binding/blocking factor, (iv) basophil activation, (v) cytokines and chemokines, (vi) cellular markers, and (vii) in vivo biomarkers. Despite their potential, most biomarkers remain infeasible to be translated to the clinical setting due to requirements of complex instruments such as flow cytometry. The identification of suitable biomarkers remains key in predicting outcomes of AIT and requires more research. Additional exploration into integrative biomarkers may be required.
目前尚无生物标志物可准确预测变应原免疫治疗(AIT)的临床结局,并将应答者与无应答者区分开来。因此,确定可靠的预测性生物标志物对于使临床医生能够进行个性化治疗至关重要。目前正在探索 AIT 生物标志物的新进展,确定关键的发展领域及其在临床中的可行性非常重要。生物标志物可大致分为七个领域:(i)免疫球蛋白 E(IgE),(ii)IgG 和 IgA 反应,(iii)IgE 介导的过敏原结合/阻断因子,(iv)嗜碱性粒细胞活化,(v)细胞因子和趋化因子,(vi)细胞标志物和(vii)体内生物标志物。尽管具有潜在的可能性,但由于需要流式细胞仪等复杂仪器,大多数生物标志物仍难以转化为临床环境。确定合适的生物标志物仍然是预测 AIT 结局的关键,需要进一步研究。可能需要进一步探索综合生物标志物。