Component-resolved diagnosis of pollen allergy based on skin testing with profilin, polcalcin and lipid transfer protein pan-allergens

被引:94
作者
Barber, D. [1 ]
de la Torre, F. [2 ]
Lombardero, M. [1 ]
Antepara, I. [3 ]
Colas, C. [4 ]
Davila, I. [5 ]
Tabar, A. I. [6 ]
Vidal, C. [7 ]
Villalba, M. [8 ]
Salcedo, G. [9 ]
Rodriguez, R. [8 ]
机构
[1] ALK Abello, Dept I D, E-28037 Madrid, Spain
[2] ALK Abello, Med Mkt, Madrid, Spain
[3] Hosp Basurto, Serv Alergia, Vizcaya, Spain
[4] Hosp Clin, Serv Alergia, Zaragoza, Spain
[5] Univ Hosp, Serv Alergia, Salamanca, Spain
[6] Hosp Virgen de Camino, Serv Alergia, Pamplona, Spain
[7] Hosp Conxo, Serv Alergia, Coruna, Spain
[8] Univ Complutense, Fac Ciencias Quim, Dept Bioquim & Biol Mol, E-28040 Madrid, Spain
[9] Univ Politecn Madrid, ETS Ingenieros Agronomos, Dept Biotecnol, Unidad Bioquim, Madrid, Spain
关键词
component-resolved diagnosis; lipid-transfer protein; pan-allergen; polcalcin; profilin; HOUSE-DUST MITE; RELEVANT ALLERGENS; CROSS-REACTIVITY; MAJOR ALLERGEN; FOLLOW-UP; IMMUNOTHERAPY; SENSITIZATION; PURIFICATION; EXPRESSION; MARKER;
D O I
10.1111/j.1365-2222.2009.03351.x
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background Allergy diagnosis needs to be improved in patients suffering from pollen polysensitization due to the existence of possible confounding factors in this type of patients. Objective To evaluate new diagnostic strategies by comparing skin responses to pan-allergens and conventional allergenic extracts with specific IgE (sIgE) to purified allergen molecules. Methods One thousand three hundred and twenty-nine pollen-allergic patients were diagnosed by a combination of an in vitro method with a panel of 13 purified allergens, including major allergens and pan-allergens, using a high-capacity screening technology (ADVIA-Centaur (R)) and skin prick test (SPT) to pan-allergens and conventional extracts. Results There was a high concordance (kappa index) between in vitro (sIgE to major allergens) and in vivo (SPT to conventional extracts) methods in patients who were not sensitized to pan-allergens, but SPT with conventional extracts failed to diagnose patients with sensitization to pan-allergens. In patients who were simultaneously sensitized to polcalcins and profilins, there was a duplication both in the number of sensitizations to major allergens and in the years of disease evolution. There was a statistical association between sensitization to profilins and/or lipid transfer proteins and food allergy (P < 0.0001). Conclusion The novel diagnostic strategy has proven to be a valuable tool in daily clinical practice. Introduction of routine SPT to pan-allergens is a simple and feasible way of improving diagnostic efficacy. Patients sensitized to pan-allergens should be tested by an adequate panel of allergenic molecules in order to identify the allergens that are responsible for the allergic disease.
引用
收藏
页码:1764 / 1773
页数:10
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