A New Reliable Method for Detecting Specific IgE Antibodies in the Patients with Immediate Type Wheat Allergy due to Hydrolyzed Wheat Protein: Correlation of Its Titer and Clinical Severity

被引:13
作者
Nakamura, Masashi [1 ,2 ]
Yagami, Akiko [1 ]
Hara, Kazuhiro [2 ]
Sano, Akiyo [1 ]
Kobayashi, Tsukane [1 ]
Aihara, Michiko [3 ]
Hide, Michihiro [4 ]
Chinuki, Yuko [5 ]
Morita, Eishin [5 ]
Teshima, Reiko [6 ]
Matsunaga, Kayoko [1 ]
机构
[1] Fujita Hlth Univ, Sch Med, Dept Dermatol, Toyoake, Aichi 4701192, Japan
[2] Hoyu Co Ltd, Gen Res & Dev Inst, Aichi, Japan
[3] Yokohama City Univ, Grad Sch Med, Dept Environm Immunodermatol, Kanagawa, Japan
[4] Hiroshima Univ, Inst Biomed & Hlth Sci, Dept Dermatol, Hiroshima, Japan
[5] Shimane Univ, Fac Med, Dept Dermatol, Matsue, Shimane, Japan
[6] Natl Inst Hlth Sci, Tokyo, Japan
关键词
enzyme-linked immunosorbent assay; Glupearl; 19S; hydrolyzed wheat protein; immediate-type wheat allergy; test method; COSMETICS;
D O I
10.2332/allergolint.13-OA-0618
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: Immediate-type wheat allergy caused by a specific hydrolyzed wheat protein (HWP-IWA), Glupearl 19S (GP19S), typically develops food-dependent exercise-induced anaphylaxis (FDEIA), but is different from conventional FDEIA, or simple wheat allergy in many aspects. The skin prick test (SPT) is considered to be the most effective method for diagnosis of HWP-IWA. As SPT is a relatively qualitative method, we developed quantitative and high-throughput test method for HWP-IWA. Methods: An enzyme-linked immunosorbent assay (ELISA)-based GP19S-specific IgE assay was tested using sera from 14 HWP-IWA and five conventional wheat-dependent exercise-induced anaphylaxis (CO-WDEIA) patients, as well as five healthy subjects. Then a validation study at five different institutions was carried out using sera from 10 HWP-IWA and five CO-WDEIA patients, as well as five healthy subjects different from the previous studies. Results: The mean unit values converted from measured absorbance of ELISA were 68.3, 1.3 and 1.1 respectively. Furthermore, the validation study revealed reproducible results across all five institutions, with the standard deviation (SD) being 0.3-0.4 for the healthy group, 0.2-0.6 for the CO-WDEIA group, and 3.8-9.6 for HWP-IWA group except for one case. One case of HWP-IWA was excluded from analysis due to the high SD of 53.3 units, indicating that samples with a unit value > 100.0 will affect inter-laboratory reproducibility. Conclusions: Our findings suggest that the ELISA-based GP19S-specific IgE assay can be used to test HWP-IWA using venous blood samples, except for those with a unit value > 100.0.
引用
收藏
页码:243 / 249
页数:7
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