A CD40 Kozak sequence polymorphism and susceptibility to antibody-mediated autoimmune conditions: the role of CD40 tissue-specific expression

被引:83
作者
Jacobson, E. M.
Huber, A. K.
Akeno, N.
Sivak, M.
Li, C. W.
Concepcion, E.
Ho, K.
Tomer, Y.
机构
[1] Univ Cincinnati, Coll Med, Div Endocrinol, Vontz Ctr Mol Med, Cincinnati, OH 45267 USA
[2] Mt Sinai, Sch Med, Dept Neurol, New York, NY USA
[3] Mt Sinai, Sch Med, Dept Med, New York, NY USA
[4] Univ Cincinnati, Coll Med, Cincinnati VA Med Ctr, Cincinnati, OH 45267 USA
关键词
thyroid; polymorphism; autoimmunity; association; B cells;
D O I
10.1038/sj.gene.6364375
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Previously, we and others have demonstrated the association of a C/T single nucleotide polymorphism ( SNP), in the Kozak sequence of CD40, with Graves' disease (GD). Here, using an expanded data set of patients, we confirm the association of the CD40 SNP with GD (n = 210, P = 0.002, odds ratio ( OR) = 1.8). Subset analysis of patients with persistently elevated thyroid peroxidase (TPO) and/or thyroglobulin (Tg) antibodies (Abs), (TPO/Tg Abs), after treatment ( n 126), revealed a significantly stronger association of the SNP with disease ( P = 5.2 x 10(-5), OR = 2.5) than in GD patients who were thyroid antibody-negative. However, the CD40 SNP was not associated with TPO/Tg Abs in healthy individuals. Next, we tested the CD40 SNP for association with Myasthenia Gravis (MG), which, like GD is an antibody-mediated autoimmune condition. Analysis of 81 MG patients found no association of the SNP with disease. Functional studies revealed significant expression of CD40 mRNA and protein in the thyroid ( target tissue in GD) but not in skeletal muscle ( target tissue in MG). Combined, our genetic and tissue expression data suggest that the CD40 Kozak SNP is specific for thyroid antibody production involved in the etiology of GD. Increased thyroidal expression of CD40 driven by the SNP may contribute to this disease specificity.
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页码:205 / 214
页数:10
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