Departments of Medical Biology & Genetics, Karadeniz Technical University, Trabzon, Turkey.
Int J Rheum Dis. 2012 Dec;15(6):538-45. doi: 10.1111/j.1756-185X.2011.01604.x. Epub 2011 Mar 4.
The aim of this study was to investigate the associations between human leukocyte antigen (HLA)-DRB1 alleles with genetic susceptibility to rheumatoid arthritis (RA) and production of antibodies against cyclic citrullinated peptide (anti-CCP antibody) and rheumatoid factor (RF) in Turkish RA patients.
We studied 291 RA patients and 253 controls. Genotyping was performed by polymerase chain reaction with sequence-specific oligonucleotide probes hybridization method. Serum levels of anti-CCP antibody, IgM-RF and high sensitive C-reactive protein titers were measured by commercial kits using immunological methods.
We found that HLA-DRB104 and 09 alleles were associated in anti-CCP+ and anti-CCP+ RA patients (P < 0.0001 and P < 0.001, respectively), while DRB101 and 04 were determined to be higher in RF+ RA patients (P < 0.001 and P < 0.0001, respectively). Moreover, DRB111 and DRB113 alleles were determined to be lower in RF and anti-CCP/RF+ RA patients (P < 0.001 for both). HLA-DRB104 was identified as a common responsible allele for susceptibility to the disease in anti-CCP, RF and anti-CCP/RF- RA patients (P = 0.0018, P = 0.0004 and P = 0.0023, respectively). HLA-DRB113 allele alone was found to be protective against to anti-CCP+ and RF- RA (P = 0.0003 and P = 0.006, respectively). On the contrary, there was no protective allele in anti-CCP/RF- RA as well as anti-CCP- RA patients.
This study indicates that associate and protective HLA-DRB1 allele distributions are different in autoantibody (anti-CCP or RF or anti-CCP/RF)+ RA and autoantibody- RA patients, with exceptions of DRB104 and DRB113.
本研究旨在探讨人类白细胞抗原(HLA)-DRB1 等位基因与土耳其类风湿关节炎(RA)患者遗传易感性及抗环瓜氨酸肽(抗-CCP 抗体)和类风湿因子(RF)产生的相关性。
我们研究了 291 例 RA 患者和 253 例对照者。采用聚合酶链反应-序列特异性寡核苷酸探针杂交方法进行基因分型。采用免疫学法,用商业试剂盒检测血清抗-CCP 抗体、IgM-RF 和高敏 C 反应蛋白滴度。
我们发现 HLA-DRB104 和 09 等位基因与抗-CCP+和抗-CCP+RA 患者相关(P<0.0001 和 P<0.001),而 DRB101 和 04 在 RF+RA 患者中较高(P<0.001 和 P<0.0001)。此外,DRB111 和 DRB113 等位基因在 RF 和抗-CCP/RF+RA 患者中较低(两者均 P<0.001)。HLA-DRB104 被确定为抗-CCP、RF 和抗-CCP/RF-RA 患者疾病易感性的共同责任等位基因(P=0.0018、P=0.0004 和 P=0.0023)。单独发现 HLA-DRB113 等位基因对抗-CCP+和 RF-RA 具有保护作用(P=0.0003 和 P=0.006)。相反,在抗-CCP/RF-RA 和抗-CCP-RA 患者中没有保护性等位基因。
本研究表明,自身抗体(抗-CCP 或 RF 或抗-CCP/RF)+RA 和自身抗体-RA 患者的关联和保护性 HLA-DRB1 等位基因分布不同,除了 DRB104 和 DRB113。