Matri Samira, Boubaker Jalel, Hamzaoui Samir, Bardi Rafika, Ayed Khaled, Filali Azza
Tunis Med. 2003 May;81(5):289-94.
Genetic factors, among which the HLA class II coding genes, are implicated in IBD pathogenesis. When considering the ethnic heterogeneity of the studied population and the IBD clinical heterogeneity, UC appears more dependent to HLA genes than CD. UC and HLA genes: HLA DR 4 gene would protect from UC. HLA DR2 gene, particularly the DRB 1 * 1502 allele, is predisposing for more severe forms necessitating a corticotherapy, while DRB 1 * 0301 allele is associated with less needs for surgery. CD and HLA genes: HLA DR 7 gene and the DRB 3 * 0301 allele predispose to CD, while HLA DR 2 and DR 3 genes may be protective factors. Thus, for MC patient, the DRB 1 * 0301/DQB*0201 haplotype might be associated with less occurrence of fistulas or severe forms requiring immunosuppressive therapy.
遗传因素,其中HLA II类编码基因与炎症性肠病(IBD)的发病机制有关。考虑到所研究人群的种族异质性和IBD的临床异质性,溃疡性结肠炎(UC)似乎比克罗恩病(CD)更依赖于HLA基因。UC与HLA基因:HLA DR4基因可预防UC。HLA DR2基因,特别是DRB11502等位基因,易导致更严重的形式,需要进行皮质激素治疗,而DRB10301等位基因与较少的手术需求相关。CD与HLA基因:HLA DR7基因和DRB30301等位基因易患CD,而HLA DR2和DR3基因可能是保护因素。因此,对于微小结肠炎(MC)患者,DRB10301/DQB*0201单倍型可能与较少发生瘘管或需要免疫抑制治疗的严重形式相关。