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Identification of autoantigens in autoimmune haemolytic anaemia by a non‐radioisotope immunoprecipitation method
Author(s) -
Barker R. N.,
Casswell K. M.,
Reid M. E.,
Sokol R. J.,
Elson C. J.
Publication year - 1992
Publication title -
british journal of haematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.907
H-Index - 186
eISSN - 1365-2141
pISSN - 0007-1048
DOI - 10.1111/j.1365-2141.1992.tb04604.x
Subject(s) - autoantibody , immunoprecipitation , antigen , antibody , hemagglutination , microbiology and biotechnology , chemistry , coombs test , red blood cell , monoclonal antibody , band 3 , abo blood group system , epitope , serology , biology , immunology , biochemistry , membrane protein , membrane
Summary In human autoimmune anaemia (AIHA), warm autoantibodies frequently appear to have serological specificity for the Rh complex, but to date, immunochemical techniques have failed to demonstrate that the antibodies react with Rh‐associated polypeptides. We describe the immunoprecipitation of red blood cell (RBC) autoantigens. using biotin labelling and a luminescent detection method. In three cases of warm AIHA, a band of 32 kD and a diffuse zone of 38–51 kD or 40–51 kD were specifically precipitated by eluted RBC autoantibody. This pattern corresponds closely with that precipitated by two Rh‐specific monoclonal antibodies, BRIC 207 and AB5. Antibody from the three eluates also showed serological specificity for the Rh complex in a haemagglutination assay against a panel of RBC with a range of Rh phenotypes, including rare ‐D‐/‐D‐and Rh null cells. Eluted autoantibody from another warm AIHA patient immunoprecipitated a peptide of 67 kD that did not correspond in apparent molecular mass either with Rh‐associated bands, or with major RBC membrane proteins or sialoglyco‐proteins (SGP). The haemagglutination assay showed that this eluate contained both Rh‐specific and Rh‐unrelated antibody. Warm autoantibody eluted from the RBC of a clinically normal, but direct antiglobulin test positive, blood donor was serologically unreactive with the Rh complex, and immunoprecipitated unknown peptides of 26, 29, 35,48 and 51 kD, together with a band of 90 kD that comigrated with SGPα 2 (glycophorin A). In six further warm AIHA cases, no antigens were precipitated by autoantibody‐containing RBC eluates. Overall, the results demonstrate that autoantibodies bind to Rh polypeptides in some, but not all, patients with warm AIHA, suggesting that the aetiology of the disease may vary.