Monoclonal antibodies against the major allergen of Plantago lanceolata pollen, Pla 1 1:: affinity chromatography purification of the allergen and development of an ELISA method for Pla 1 1 measurement

被引:17
|
作者
Calabozo, B [1 ]
Duffort, O [1 ]
Carpizo, JA [1 ]
Barber, D [1 ]
Polo, F [1 ]
机构
[1] ALK Abello, Dept Invest & Desarrollo, Dept Res & Dev, E-28037 Madrid, Spain
关键词
cross-reactivity; immunoassay; monoclonal antibody; Pla; 1; Plantago lanceolata; plantain; pollinosis;
D O I
10.1034/j.1398-9995.2001.056005429.x
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: Plantngo lanceolata (English plantain) pollen is a relevant cause of pollinosis in temperate regions. The major allergen of this pollen, Pla 1 1, is recognized by the specific IgE from more than 80% of plantain-sensitive patients. It displays significant sequence homology with the major olive-pollen allergen Ole e 1. The objective was to develop a monoclonal antibody-based ELISA to quantify Pla 1 1, and to assess the correlation of Pla 1 1 content with the biologic activity of plantain pollen extracts. We also aimed to establish the specificity of the monoclonal antibodies against the potentially cross-reactive allergen Ole e 1, and to investigate the presence of Pla 1 1-like proteins in psyllium and melon that have been reported to cross-react with P. lanceolata pollen. Methods: After fusion of myeloma cells with spleen cells from a BALB/c mouse, two Pla 1 1-specific monoclonal antibodies secreting hybridomas were selected, and the antibodies characterized. One of them (2A10) was used as the capture antibody in an ELISA for Pla 1 1 quantitation. An anti-P. lanceolata rabbit serum was used as the second antibody. Pla 1 1 was purified by immunoaffinity chromatography and used as the standard in the assay. Results: The ELISA developed was highly reproducible and sensitive, with a detection limit of 0.1 ng/ml, and a practical working range of 0.4-12 ng/ml. The specificity was demonstrated against a large battery of allergens, including Ole e i. The concentration of Pla 1 1 was measured in 19 extracts of P. lanceolata pollen, and a good correlation was observed between the Pla 1 1 content and the allergenic activity of the extracts. Pla 1 1 was not detected in psyllium or melon extracts. Conclusions: The results prove the usefulness of the Pla 1 1-ELISA for the standardization of extracts of P. lanceolata pollen intended for clinical use.
引用
收藏
页码:429 / 435
页数:7
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