Djilali-Saiah I, Ouellette P, Caillat-Zucman S, Debray D, Kohn J I, Alvarez F
Gastroenterology Division, Hôpital Sainte-Justine, Montreal, Quebec, Canada.
Hum Immunol. 2001 Dec;62(12):1356-62. doi: 10.1016/s0198-8859(01)00344-5.
Susceptibility to autoimmune hepatitis is associated with particular human leucocyte antigen class II alleles. However, non-HLA genetic factors are likely to be required for development of the disease. Among the candidate genes, the cytotoxic T-lymphocyte antigen 4 (CTLA-4) and CD28 genes, located on chromosome 2q33 in humans, encode a cell surface molecule playing a dominant role in the regulation of T-cell activation. The CTLA-4 and CD28 polymorphisms were investigated in children from 32 families with autoimmune hepatitis (AIH). The transmission/disequilibrium test revealed increased transmission of the (AT)8 (dinucleotide repeat) and A (exon 1) alleles of CTLA-4 gene from heterozygous parents to affected offspring (87.5% and 83.5%) with type 1 AIH, compared with unaffected offspring (50.0% for both, p = 0.009 and 0.02, respectively). In contrast, no deviation in transmission for CTLA-4 polymorphisms was found between type 2 AIH patients and unaffected offspring. No evidence for association was found between CD28 gene polymorphism or D2S72 genetic marker and both types of AIH. This study identified the CTLA-4 gene polymorphism as a non-HLA determinant that predisposes to AIH type 1 in children. The genetic heterogeneity seen in the present study provides a new argument in favor of pathogenic differences between type 1 and type 2 AIH.
自身免疫性肝炎的易感性与特定的人类白细胞抗原II类等位基因相关。然而,该疾病的发生可能还需要非HLA遗传因素。在候选基因中,位于人类2号染色体q33的细胞毒性T淋巴细胞抗原4(CTLA-4)和CD28基因,编码一种在T细胞活化调节中起主导作用的细胞表面分子。对来自32个自身免疫性肝炎(AIH)家庭的儿童进行了CTLA-4和CD28基因多态性研究。传递/不平衡检验显示,CTLA-4基因的(AT)8(二核苷酸重复序列)和A(外显子1)等位基因从杂合子父母向1型AIH的患病后代传递增加(分别为87.5%和83.5%),而向未患病后代传递的比例为50.0%(两者均为50.0%,p分别为0.009和0.02)。相比之下,2型AIH患者与未患病后代之间未发现CTLA-4基因多态性传递存在偏差。未发现CD28基因多态性或D2S72遗传标记与两种类型的AIH存在关联。本研究确定CTLA-4基因多态性是儿童1型AIH的一种非HLA决定因素。本研究中观察到的遗传异质性为支持1型和2型AIH之间的致病差异提供了新的论据。