Instituto Nacional de Enfermedades Respiratorias Ismael Cosio Villegas, Tlalpan 4502, Sección XVI, CP 14080, México City, DF, Mexico.
Respir Med. 2010 Jun;104(6):889-94. doi: 10.1016/j.rmed.2010.01.014. Epub 2010 Feb 11.
Hypersensitivity Pneumonitis (HP) is a lung inflammatory disorder caused by inhalation of organic particles by a susceptible host. However, only a small proportion of individuals exposed to HP-associated antigens develop the disease, suggesting that additional host/environmental factors may play a role. We have previously found that genetic susceptibility associated to the major histocompatibility complex (MHC) plays an important role in this disease. The low molecular weight proteosome (LMP, currently named PSMB) genes code for subunits of the proteosome, a multimeric enzymatic complex that degrades proteins into peptides in order to be presented in the MHC class I pathway. We hypothesized that polymorphisms in PSMB8 or PSMB9 genes could be involved in the susceptibility to HP. Thus, in this study we analyzed the polymorphic site at amino acid position 60 (Arg/His) of the fourth exon in the PSMB9 gene and the amino acid position 49 (Gln/Lys) in the second exon of PSMB8 gene in 50 Mexican patients with HP and 50 healthy ethnically matched controls. PSMB typing was performed using polymerase chain reaction-restriction fragment length polymorphisms (PCR-RFLP). Our results demonstrated that HP patients had a significant increase of the PSMB8 KQ genotype frequency (OR = 7.25, CI = 2.61-21.3; p = 0.000034). No differences were found in the distribution of PSMB9 alleles/genotypes. However, PSMB9-RH/PSMB8 KQ haplotype was significantly increased in HP patients (OR = 6.77, CI = 1.34-65.31, p < 0.02). These findings suggest that PSMB8 KQ genotype could increase the risk to develop hypersensitivity pneumonitis.
过敏性肺炎(HP)是一种由宿主吸入有机颗粒引起的肺部炎症性疾病。然而,只有一小部分接触 HP 相关抗原的个体发展为这种疾病,这表明其他宿主/环境因素可能起作用。我们之前发现,主要组织相容性复合体(MHC)相关的遗传易感性在这种疾病中起着重要作用。低分子量蛋白酶体(LMP,目前称为 PSMB)基因编码蛋白酶体的亚基,蛋白酶体是一种多聚酶复合物,可将蛋白质降解成肽,以便在 MHC Ⅰ类途径中呈递。我们假设 PSMB8 或 PSMB9 基因的多态性可能与 HP 的易感性有关。因此,在这项研究中,我们分析了 50 例墨西哥 HP 患者和 50 例匹配的健康对照者的 PSMB9 基因第四外显子第 60 位(精氨酸/组氨酸)和 PSMB8 基因第二外显子第 49 位(谷氨酰胺/赖氨酸)的多态性。使用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)进行 PSMB 分型。我们的结果表明,HP 患者的 PSMB8 KQ 基因型频率显著增加(OR=7.25,CI=2.61-21.3;p=0.000034)。PSMB9 等位基因/基因型的分布无差异。然而,PSMB9-RH/PSMB8 KQ 单倍型在 HP 患者中显著增加(OR=6.77,CI=1.34-65.31,p<0.02)。这些发现表明 PSMB8 KQ 基因型可能增加患过敏性肺炎的风险。