Linear IgA disease: the IgA and IgG response to dermal antigens demonstrates a chiefly IgA response to LAD285 and a dermal 180-kDa protein

被引:22
作者
Allen, J [1 ]
Wojnarowska, F [1 ]
机构
[1] Oxford Radcliffe Hosp, Dept Dermatol, Oxford OX3 7LJ, England
关键词
antibody isotype; dermal extracts; immunoblotting; LAD285; linear IgA disease; target antigens;
D O I
10.1111/j.1365-2133.2003.05647.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background Background Linear IgA disease (LAD) of adults and children is mediated by IgA antibodies that target proteins of the epithelial adhesion complex. Most studies have concentrated on the epidermal-associated antigens; the dermal antigens remain unresolved. Objectives To determine the dermal antigen repertoire of IgA and IgG antibodies in LAD. Methods Immunoblotting was carried out on salt-split and urea-extracted dermal skin extracts with IgA antibodies (63 adult and 34 childhood sera) and with IgG antibodies (49 adult and 18 childhood sera). Results Antigens were identified by IgA (61%), IgG (27%) and by both antibody isotypes (19%). LAD285 and an antigen of 180 kDa were the major dermal antigens identified, and antigens of 230 kDa, collagen VII and a protein under 100 kDa were identified less commonly. IgA autoantibodies from adults bound single antigens more frequently than multiple antigens; from children they bound single and multiple antigens equally. The binding of multiple antigens was, however, more common in children than adults. The IgG response was weaker. The 180-kDa antigen was the main IgG dermal target, and with a single exception, IgG autoantibodies targeted single antigens. Conclusions There was an IgA and IgG response to dermal antigens in LAD; however, the dual antibody response was limited. The antibody response to LAD285 and a 180-kDa antigen (probably BP180) suggests that intermolecular epitope spreading of the antigens associated with the extracellular matrix/dermal components of the basement membrane contributes to the immunopathology of the disease. The restricted IgG response suggests that dermal-binding IgG autoantibodies are not pathologically significant.
引用
收藏
页码:1055 / 1058
页数:4
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