Detection of specific antibodies to pigeon serum and bloom antigens by enzyme linked immunosorbent assay in pigeon breeder's disease

Citation
Mj. Rodrigo et al., Detection of specific antibodies to pigeon serum and bloom antigens by enzyme linked immunosorbent assay in pigeon breeder's disease, OCC ENVIR M, 57(3), 2000, pp. 159-164
Citations number
27
Categorie Soggetti
Envirnomentale Medicine & Public Health","Pharmacology & Toxicology
Journal title
OCCUPATIONAL AND ENVIRONMENTAL MEDICINE
ISSN journal
13510711 → ACNP
Volume
57
Issue
3
Year of publication
2000
Pages
159 - 164
Database
ISI
SICI code
1351-0711(200003)57:3<159:DOSATP>2.0.ZU;2-O
Abstract
Background-Pigeon breeder's disease is an extrinsic allergic alveolitis in the lungs of sensitised people, caused by hypersensitivity reactions to inh aled pigeon antigens. Antigens from different sources of the animal are use d for diagnostic purposes, with serum being the most widely used. Bloom is rarely used; very little is known of its antigenicity and diagnostic perfor mance, particularly when used with the enzyme linked immunosorbent assay (E LISA) method, which is the most popular test as it permits measurement of t he antibody response. Methods-To (a) standardise an ELISA for the measurement of specific IgG aga inst pigeon serum and pigeon bloom extract; (b) to establish reference valu es for specific IgG in 73 non-exposed controls, (c) to show the presence of specific IgG against pigeon serum and bloom in serum samples of 17 patient s with bird fancier's lung and 11 asymptomatic fanciers, and (d) to study t he similarity of the two antigen sources by cross reactivity experiments. Results-Reference values of specific IgG were defined with the 97.5 percent ile (367.9 U/ml for pigeon serum and 953.7 U/ml for pigeon bloom extract). Of symptomatic patients 100% had values higher than the cut off for both an tigens. In asymptomatic fanciers values were higher than the cut off for pi geon serum in 45% and bloom extract in 54%. Cross reactivity experiments sh owed that the two antigens differed in antigenic content although some comp onents may be common to both. Conclusion-The ELISA methods used proved to be useful tools for evaluating specific IgG antibody responses against both antigens. The diagnostic perfo rmance of both ELISA methods performed with these antigen sources was simil ar, showing very high sensitivity but moderate specificity. Although some a ntigenic similarity was found between pigeon serum and bloom extract, cross reactivity studies showed that various antigens seemed to be specific to t he bloom extract. However, the antigens responsible for pigeon breeder's di sease seem to be present in both antigenic sources.