Purification of the antigenic components of pigeon dropping extract, the responsible agent for cellular immunity in pigeon breeder's disease

被引:24
作者
Hisauchi-Kojima, K
Sumi, Y
Miyashita, Y
Miyake, S
Toyoda, H
Kurup, VP
Yoshizawa, Y
机构
[1] Tokyo Med & Dent Univ, Dept Pulm Med, Bunkyo Ku, Tokyo 1138519, Japan
[2] Univ Calif Los Angeles, Sch Med, Cedars Sinai Med Ctr, Div Med Genet, Los Angeles, CA USA
[3] Med Coll Wisconsin, VAMC, Dept Med, Milwaukee, WI 53226 USA
关键词
pigeon breeder's disease; antigen purification; sodium dodecylsulfate-polyacrylamide gel electrophoresis; 2-dimensional electrophoresis; immunoblotting; cellular immune response; N-terminal sequence of peptide; synthetic peptides;
D O I
10.1016/S0091-6749(99)70193-4
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: Pigeon breeder's disease (PBD) is a lung disease caused by inhalation of antigens derived from pigeons. Objective: This study was undertaken to characterize the responsible component of pigeon dropping extract (PDE) for PBD. Methods: First, crude PDE was applied to SDS-PAGE followed by immunoblotting by using antibodies in bronchoalveolar lavage (BAL) fluid. Second, 9 bands of PDE were separated by SDS-PAGE and used for antigen-induced PBMCs. Finally, amino-terminal sequencing was conducted on an isolated 21-kd protein by 2-dimensional electrophoresis. Results: Immunoblots with BAL fluid from patients with PBD identified 9 bands. Similar patterns were observed by using BAL fluid from 10 control patients (9 with summer-type hypersensitivity pneumonitis of idiopathic pulmonary fibrosis and 1 asymptomatic breeder), except for the 21-kd protein, which was detected in 10 patients with PBD and 1 asymptomatic breeder. The stimulation indices of PBMCs determined by using proteins electroeluted from the 9 bands were higher in patients with PBD than in the 10 control patients. The 21-kd protein was separated into 5 spots by 2-dimensional electrophoresis; these spots were all reactive with BAL fluid from patients with PBD as determined by immunoblotting. The sequence of the 21-kd protein had 57% identity to a Saccharomyces cerevisiae chromosome X reading frame. A synthetic peptide, derived from the amino acid sequence of the N-terminal of the native protein, induced significant proliferation of PBMCs obtained from 5 patients with PBD, but not with PBMCs obtained from control patients. Conclusion: The 21-kd protein is the only protein that identified individuals exposed to pigeons by immunoblotting. Only PBMCs from patients with PBD showed significant proliferation to the 21-kd protein and to the synthetic peptide on the basis of the N-terminal sequence of the native peptide. The 21-kd protein will be an important antigen for studies on the epidemiology, diagnosis, and pathogenesis of PBD.
引用
收藏
页码:1158 / 1165
页数:8
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