Open AccessStructural polymorphisms of complement receptor 1 (CR1) in systemic lupus erythematosus (SLE) patients and normal controls of three ethnic groups
Author(s) -
MOULDS J. M.,
REVEILLE J. D.,
ARNETT F. C.
Publication year - 1996
Publication title -
clinical & experimental immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.329
H-Index - 135
eISSN - 1365-2249
pISSN - 0009-9104
DOI - 10.1046/j.1365-2249.1996.d01-748.x
Subject(s) - immunology , ethnic group , medicine , complement system , complement (music) , systemic lupus erythematosus , lupus erythematosus , biology , antibody , genetics , gene , disease , phenotype , political science , complementation , law
CR1 exhibits a molecular weight polymorphism and variability in the number of C3b‐binding sites. Because this may affect immune complex clearance, we used erythrocytes to investigate the CR1 size polymorphism in SLE patients from three ethnic groups. The CR1‐C allele was found more frequently in African–Americans, but the frequency did not differ between controls (10%, n = 63) and SLE patients (9%, n = 79). A 160‐kD band similar to CR1‐C was noted in a number of patients and was shown to be a proteolytic cleavage fragment. The study shows that the smallest form of CR1, i.e. CR1‐C, is not a genetic risk factor for SLE and that the frequencies of the CR1 structural alleles do not differ from race‐matched healthy controls.