The skin prick test response after allergen immunotherapy in different levels of tIgE children with mite sensitive Asthma/Rhinitis in South China. Issue 10 (3rd October 2018)

• Record Type: Journal Article
• Authors: Sun, Wangming; Pan, Lingzhi; Yu, Qiying; Sun, Yan; Zeng, Xiangyan; Bai, Xiaoli; Li, Mengrong
• Is Part Of: Human vaccines & immunotherapeutics. Volume 14:Issue 10(2018)
• Page Start: 2510
• Page End: 2515
• Publication Date: 2018-10-03
• Subjects: Asthma -- Allergen immunotherapy -- Efficacy -- Skin prick test -- Total IgE; Vaccines -- Periodicals; 615.372
• DOI: 10.1080/21645515.2018.1482171
• Languages: English
• ISSNs: 2164-5515

Abstract

ABSTRACT: Background: At present, the biomarkers which can predict the clinical efficacy of allergen immunotherapy (AIT) are still much debated. IgE levels are often related to allergic severity. Therefore, this study aimed at relating total IgE (tIgE) levels with the efficacy of AIT assessed by symptoms and drug score and skin prick test (SPT) response. Methods: We evaluated 81 allergic children who had received house-dust mite (HDM) subcutaneous immunotherapy for three years. According to the tIgE levels before treatment, all children were divided into high value, medium value and low value group. Each group according to sIgE/tIgE ratio was divided into subgroups. The efficacy of AIT is assessed by symptoms and drug score. By comparing changes in the grade of SPT in each group, the response of AIT are evaluated. Results: The SPT grade changes to determine efficacy had a high degree of consistency with symptoms and drug score judgment (sensitivity 89.7%, specificity 78.3%, Kappa = 0.670, P < 0.001). Compared to ineffective cases, the effective cases had lower tIgE ( P < 0.001) and higher ratio of sIgE/tIgE ( P < 0.001). The grades of SPT declined the most in the low value group (low value group vs. medium value group, P < 0.05; low value group vs. high value group, P < 0.001; medium value group vs. high value group, P < 0.05). Conclusions: The SPT grade change can be used for efficacy evaluation. Children with lower level of tIgE and higher ratio of sIgE/tIgE that obtain a more satisfactory effect.