| Title | Circulating anti-glomerular basement membrane autoantibodies against a3(IV)NC1 undetectable by commercially available enzyme-linked immunosorbent assays |
| Authors | Jia, Xiao-Yu Qu, Zhen Cui, Zhao Yang, Rui Zhao, Juan Zhao, Ming-Hui |
| Affiliation | Peking Univ, Div Renal, Dept Med,Hosp 1, Inst Nephrol,Key Lab Renal Dis,Minist Hlth China, Beijing 100034, Peoples R China. Peking Univ, Div Renal, Dept Med,Hosp 1, Inst Nephrol,Key Lab Renal Dis,Minist Hlth China, 8 Xishiku St, Beijing 100034, Peoples R China. |
| Keywords | anti-glomerular basement membrane disease conformational structure epitope Goodpasture disease a3(IV)NC1 RESONANT MIRROR BIOSENSOR GOODPASTURES-SYNDROME ALPHA-3(IV) COLLAGEN CRYPTIC EPITOPES NC1 DOMAIN DISEASE ANTIBODIES ANTIGEN GLOMERULONEPHRITIS AUTOANTIGEN |
| Issue Date | 2012 |
| Publisher | nephrology |
| Citation | NEPHROLOGY.2012,17,(2),160-166. |
| Abstract | Aim: Cases with anti-glomerular basement membrane (GBM) disease have been reported with linear deposit of immunoglobulin G (IgG) along GBM, but have undetectable anti-GBM antibodies in circulation by enzyme linked immunosorbent assays (ELISA). We speculated that the structure of the antigens recognized by these antibodies may contribute to the negative results of ELISA. Methods: Sera from four patients were collected, with typical linear deposit of IgG along GBM but no anti-GBM reactivity by commercial ELISA kits. Circulating anti-GBM antibodies were detected by indirect immunofluorescence. Antigen specificity and its conformational structure was investigated by western-blot analysis, using recombinant human alpha 1-alpha 5(IV) NC1 and chimeric proteins EA and EB as antigens. Results: The presence of circulating anti-GBM antibodies were confirmed by indirect immunofluorescence with linear deposit of IgG towards cryptic epitopes along GBM on normal kidney sections. These antibodies did not recognize recombinant human alpha 1, alpha 2, alpha 4 or alpha 5(IV)NC1, but could blot alpha 3(IV) NC1 under non-reducing non-boiling conditions on western-blot analysis, when the conformational epitope(s) on alpha 3(IV)NC1 were thought to be preserved. When alpha 3(IV) NC1 was prepared under reducing conditions with beta-mercaptoethanol and/ or boiled to destroy the disulfide bonds, the binding with the antibodies disappeared. Moreover, these antibodies recognized neither EA nor EB, indicating their distinct epitope repertoire. Conclusion: Circulating anti-GBM antibodies undetectable by ELISA could recognize cryptic and conformation-dependent epitopes restricted on alpha 3(IV) NC1, distinct from EA and EB. Indirect immunofluorescence was necessary for antibody detection and treatment monitoring under such circumstances. |
| URI | http://hdl.handle.net/20.500.11897/160170 |
| ISSN | 1320-5358 |
| DOI | 10.1111/j.1440-1797.2011.01511.x |
| Indexed | SCI(E) PubMed |
| Appears in Collections: | 第一医院 |
