HLA Class II influences humoral autoimmunity in patients with type 2 autoimmune hepatitis

被引:88
作者
Djilali-Saiah, Idriss [1 ]
Fakhfakh, Amin
Louafi, Hamida
Caillat-Zucman, Sophie
Debray, Dominique
Alvarez, Fernando
机构
[1] Hop St Justine, Div Gastroenterol, Montreal, PQ, Canada
[2] Univ Montreal, Dept Microbiol & Immunol, Montreal, PQ, Canada
[3] Hop St Vincent de Paul, INSERM, U 561, F-75674 Paris, France
[4] Hop Kremlin Bicetre, Hepatol Unit, Paris, France
关键词
human; autoimmunity; antigens/peptides/epitopes; autoantibodies; MHC;
D O I
10.1016/j.jhep.2006.07.034
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background/Aims: Type 2 autoimmune hepatitis (AIH) is characterized by the presence of anti-liver kidney microsome (anti-LKM-1) and/or anti-liver cytosol type 1 (anti-LC1) autoantibodies. However, the correlation between these autoantibodies and the genetic background has not been studied. Methods: Frequencies of HLA class II alleles were compared between the 60 Caucasian children with type 2 AIH and 313 control subjects. The anti-LKM1 antibody reactivity directed against antigenic sites of CYP2D6 was analysed by ELISA. Results: HLA-DQB1*0201 allele was found to be the primary genetic determinant of susceptibility to type 2 AIH by conferring the highest odd-ratio (OR = 6.4). HLA-DRB1*03 allele was significantly increased (P < 0.0001) among patients with both anti-LKM1 and anti-LC1 autoantibodies as well as in those with only anti-LC1(+) compared to those with anti-LKM1(+) alone. In contrast, HLA-DRB1*07 allele was significantly associated (P < 0.0001) with anti-LKM1(+) alone compared to groups with both anti-LKM1 and anti-LC1 or with LC1(+) alone. Children with the DRB1*07 allele develop anti-LKM1 autoantibodies having a more restricted specificity (2 epitopes) than to those having HLA-DRB1*03 allele (5 epitopes). Conclusions:The HLA-DR locus is involved in autoantibody expression, while the DQ locus appears to be a critical determinant for the development of type 2 AIH. (c) 2006 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:844 / 850
页数:7
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