Inherited IgA glycosylation pattern in IgA nephropathy and HSP nephritis: where do we go next?

被引:11
作者
Boyd, Joanna K. [2 ]
Barratt, Jonathan [1 ,2 ]
机构
[1] Leicester Gen Hosp, Dept Infect Immun & Inflammat, John Walls Renal Unit, Leicester LE5 4PW, Leics, England
[2] Univ Leicester, Dept Infect Immun & Inflammat, Leicester, Leics, England
关键词
O-GLYCOSYLATION; COSMC;
D O I
10.1038/ki.2011.83
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
New data from Kiryluk et al. show the importance of genetic factors in determining the profile of serum IgA1 O-glycoforms in IgA nephropathy and Henoch-Schonlein purpura nephritis. Elevated serum levels of poorly galactosylated IgA1 O-glycoforms do not, however, appear sufficient in themselves to cause nephritis in these two diseases, and a 'second hit' is necessary before changes in IgA1 glycosylation translate into clinical disease. The challenge now is to determine what these genetic factors are.
引用
收藏
页码:8 / 10
页数:3
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