Penglis P S, Bond C, Humphreys I, McCluskey J, Cleland L G
Rheumatology Department, Royal Adelaide Hospital, South Australia.
Semin Arthritis Rheum. 2000 Oct;30(2):111-20. doi: 10.1053/sarh.2000.9202.
Rheumatoid arthritis (RA) is a chronic inflammatory disease for which immunogenetic susceptibility factors have been defined. In a recent case control study, it was shown that a prior intimate relationship with pet cats or budgerigars confers risk for subsequent development of RA after a period of latency. Pets are a potential reservoir for putative microbial agents that could be a stimulus for chronic inflammation subject to the influence of immunogenetic factors. Therefore, a study was undertaken to determine whether the presence of HLA-DRB1 alleles bearing the RA susceptibility motif influenced risk for RA associated with prior exposure to pets.
Blood samples were obtained from available RA patients and their case controls who had participated in the prior epidemiologic study. DR and DQ genotypes were determined by sequence analysis of oligonucleotides amplified from the DRB1 and DQB1 genes by polymerase chain reactions (PCR). Subjects were segregated according to pet exposure (as determined previously) and genotype for statistical analyses.
The odds ratio (OR) for prepubertal exposure to cats and RA in available subjects irrespective of DRB1 genotype was 4.2 (CI, 2.1 to 8.5; P<.00002). The OR between prior exposure to cats and RA in subjects with the RA susceptibility genotype DRB1 *0401 and *0404 was 5.8 (CI, 1.4 to 26; P<.02) and >24 (CI, 1.6 to 813; P<.01), respectively. In subjects with the genotype DRB1 *1501, the association between RA and prior cat exposure was OR 8.4 (CI, 1.7 to 45; P<.01). No significant association between RA and pet exposure was found in patients selected according to other genotypes. The association between RA and the recognized HLA-DR susceptibility motif was slightly stronger in subjects with a history of intimate cat exposure (OR 4.7 [CI, 1.5 to 14.8], P<.005) than subjects without prior intimate exposure (OR 3.3 [CI; 1.2 to 9.3], P<.02). In the small number of subjects who had reported an intimate association with pet birds, no influence of DR genotype on risk for RA was discerned.
Risk for RA associated with prior intimate exposure to cats is concentrated in subjects with the RA-susceptibility conferring genotypes DRB1 *0401 and 0404. The findings suggest an interaction between an environmen-tal agent associated with pet cats and certain RA susceptibility-conferring DR genotypes. The risk for RA associated with intimate cat exposure also was significant in subjects with DRB11501, a genotype not otherwise associated with RA, but which shares with known RA susceptibility-bearing alleles the presence of an electropositive pocket (Pocket 4) in the DR peptide binding groove.
类风湿关节炎(RA)是一种已明确免疫遗传易感性因素的慢性炎症性疾病。在最近一项病例对照研究中,研究表明,此前与宠物猫或虎皮鹦鹉有亲密接触关系会在一段潜伏期后增加患RA的风险。宠物是潜在的假定微生物病原体宿主,这些病原体在免疫遗传因素的影响下可能成为慢性炎症的刺激因素。因此,开展了一项研究以确定携带RA易感基序的HLA - DRB1等位基因的存在是否会影响与先前接触宠物相关的RA风险。
从参与先前流行病学研究的现有RA患者及其病例对照中采集血样。通过聚合酶链反应(PCR)从DRB1和DQB1基因扩增的寡核苷酸序列分析来确定DR和DQ基因型。根据宠物接触情况(如先前确定的)和基因型对受试者进行分类以进行统计分析。
在现有受试者中,无论DRB1基因型如何,青春期前接触猫与RA的比值比(OR)为4.2(95%置信区间[CI],2.1至8.5;P <.00002)。在具有RA易感基因型DRB1 0401和0404的受试者中,先前接触猫与RA之间的OR分别为5.8(CI,1.4至26;P <.02)和>24(CI,1.6至813;P <.01)。在基因型为DRB1 *1501的受试者中,RA与先前接触猫之间的关联OR为8.4(CI,1.7至45;P <.01)。在根据其他基因型选择的患者中,未发现RA与宠物接触之间存在显著关联。有亲密接触猫史的受试者中,RA与公认的HLA - DR易感基序之间的关联(OR 4.7 [CI,1.5至14.8],P <.005)比无先前亲密接触史的受试者(OR 3.3 [CI;1.2至9.3],P <.02)稍强。在少数报告与宠物鸟有亲密接触的受试者中,未发现DR基因型对RA风险有影响。
先前与猫亲密接触相关的RA风险集中在具有RA易感基因型DRB1 0401和0404的受试者中。研究结果表明,与宠物猫相关的环境因素与某些RA易感DR基因型之间存在相互作用。在DRB1*1501基因型(该基因型在其他方面与RA无关,但在DR肽结合槽中与已知的携带RA易感等位基因一样存在一个正电口袋[口袋4])的受试者中,与亲密接触猫相关的RA风险也很显著。