Choonhakarn Charoen, Romphruk Amornrat, Puapairoj Chintana, Jirarattanapochai Kunya, Romphruk Arunrat, Leelayuwat Chanvit
Division of Dermatology, Department of Medicine, Faculty of Medicine, and Blood Transfusion Center, Khon Kaen University, Khon Kaen 40002, Thailand.
Int J Dermatol. 2002 Jun;41(6):330-4. doi: 10.1046/j.1365-4362.2002.01496.x.
To evaluate the distributions of the human leukocyte antigen (HLA) at class I and II loci that may contribute to the genetic susceptibility to psoriasis patients in the north-eastern Thai population.
We analyzed the allelic frequencies of HLA class I and II by using the polymerase chain reaction-amplification refractory mutation system (PCR-ARMS) technique and polymerase chain reaction-single stranded conformation polymorphism (PCR-SSCP), respectively, in 140 north-eastern Thais with psoriasis that were sudivided into two groups: one with age at onset < 40 years (type I psoriasis; 95 cases) and the other with age at onset > 40 years (type II psoriasis; 45 cases). Three hundred healthy unrelated north-eastern Thais were used as controls.
HLA-A01, -A0207, -A30, -B08, -B13, -B4601, -B57, -Cw01, -Cw0602, and -DRB107 were positively associated with type I psoriasis, whereas HLA-A24, -A33, and -Cw04 were negatively associated with type I psoriasis with statistical significance when compared to the controls. The Cw0602 allele showed the strongest correlation with this type. In addition, the frequencies of HLA-A0207, -A30, -Cw01, and -DRB11401 were significantly increased in type II psoriasis. HLA-A207, -B4601, -Cw01, -DRB109, -DQB10303 (AH46.1), HLA-A01-B57-Cw0602-DRB107-DQB10303 (AH57.1), and HLA-A30, -B13, -Cw0602, -DRB107, and -DQB1*02 (AH13.1) were identified as high-risk major histocompatibility complex (MHC) halotypes for psoriasis patients in the early onset group in north-eastern Thais.
This study demonstrates not only the differential association between HLA markers and types of psoriasis according to age at onset, but also a newly found high-risk and a protective haplotype in Thai psoriasis patients.
评估人类白细胞抗原(HLA)I类和II类基因座的分布情况,这些分布可能与泰国东北部银屑病患者的遗传易感性有关。
我们分别采用聚合酶链反应-扩增阻滞突变系统(PCR-ARMS)技术和聚合酶链反应-单链构象多态性(PCR-SSCP)分析了140例泰国东北部银屑病患者的HLA I类和II类等位基因频率。这些患者被分为两组:一组发病年龄<40岁(I型银屑病;95例),另一组发病年龄>40岁(II型银屑病;45例)。300名健康的、无亲缘关系的泰国东北部人作为对照。
HLA-A01、-A0207、-A30、-B08、-B13、-B4601、-B57、-Cw01、-Cw0602和-DRB107与I型银屑病呈正相关,而与对照组相比,HLA-A24、-A33和-Cw04与I型银屑病呈负相关,具有统计学意义。Cw0602等位基因与该型银屑病的相关性最强。此外,HLA-A0207、-A30、-Cw01和-DRB11401在II型银屑病中的频率显著增加。HLA-A207、-B4601、-Cw01、-DRB109、-DQB10303(AH46.1)、HLA-A01-B57-Cw0602-DRB107-DQB10303(AH57.1)以及HLA-A30、-B13、-Cw0602、-DRB107和-DQB1*02(AH13.1)被确定为泰国东北部早发型银屑病患者的高危主要组织相容性复合体(MHC)单倍型。
本研究不仅证明了HLA标记与根据发病年龄划分的银屑病类型之间的差异关联,还发现了泰国银屑病患者中新的高危和保护性单倍型。