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Immunochemical specificity of autoanti‐Gerbich from two patients with autoimmune haemolytic anaemia and concomitant alteration in the red cell membrane sialoglycoprotein β
Author(s) -
Reid Marion E.,
VengelenTyler Virginia,
Shulman Ira,
Reynolds Marilyn V.
Publication year - 1988
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.1365-2141.1988.tb07603.x
Subject(s) - sialoglycoprotein , autoantibody , red blood cell , red cell , biology , immunology , medicine , antibody
Summary. Blood samples from two patients with autoimmune haemolytic anaemia, whose autoantibodies failed to agglutinate certain examples of red cells that lack Gerbich blood group antigens, were studied using immunochemical analyses. One of these autoantibodies differed from all other anti‐Ge in that it showed a unique β sialoglycoprotein (SGP) specificity. It reacted with normal β but not with the abnormal β‐related SGPs associated with Gerbich‐negative red cells of the Gerbich and Yus types. Red cells from this patient had an alteration of β SGP, while the α, γ and δ SGPs appeared to be normal. The autoantibody from the other patient did not show this unique characteristic. Its immunochemical specificity was similar to alloanti‐Ge3 in that it reacted with both β and γ SGPs from normal red cell membranes and with the abnormal β‐related SGPs found in red cell membranes from individuals with Gerbich‐negative red cells of the Yus type. Red cells from this patient could not be analysed because she had recently received a massive transfusion of red cells.