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家族性斑秃:与HLA基因座的关联。

Alopecia areata in families: association with the HLA locus.

作者信息

de Andrade M, Jackow C M, Dahm N, Hordinsky M, Reveille J D, Duvic M

机构信息

Department of Epidemiology, The University of Texas MD Anderson Cancer Center, Houston 77030, USA.

出版信息

J Investig Dermatol Symp Proc. 1999 Dec;4(3):220-3. doi: 10.1038/sj.jidsp.5640215.

Abstract

Alopecia areata (AA) is a T cell mediated disease directed against hair follicles that results in bald patches. It can range in severity from patchy (AA), to total scalp hair loss (alopecia totalis; AT) or body hair loss (alopecia universalis; AU). We have previously shown that HLA-DR4 and DR11 as well as HLA-DQ*03 alleles are increased in unrelated AA patients compared with controls. To study whether class II HLA alleles are linked to AA, we investigated 81 extended families that included 192 AA patients, including 89 with AT or AU. We also performed the transmission disequilibrium test (TDT) in 143 nuclear families. Results showed an association between alleles of HLA-DQB (p = 0.014) and HLA-DR (p = 0.010). We also performed linkage analysis in 75 families whose members' genomic DNA were available for HLA typing. Results from this analysis support linkage between AA and class II loci with a maximal LOD score of 2.42 to HLA-DQB at 5% recombination, and with a maximal LOD score of 2.34 to HLA-DR at 0% recombination. There was an increased incidence of atopic dermatitis and autoimmune thyroiditis in families. AA appears to be a class II HLA restricted organ specific immune response to the hair follicle.

摘要

斑秃(AA)是一种由T细胞介导的针对毛囊的疾病,可导致秃斑。其严重程度范围从局部斑秃(AA)到全头皮脱发(全秃;AT)或全身毛发脱落(普秃;AU)。我们之前已经表明,与对照组相比,无关AA患者中HLA - DR4和DR11以及HLA - DQ*03等位基因增加。为了研究II类HLA等位基因是否与AA相关联,我们调查了81个大家庭,其中包括192名AA患者,其中89名患有AT或AU。我们还在143个核心家庭中进行了传递不平衡检验(TDT)。结果显示HLA - DQB等位基因(p = 0.014)与HLA - DR等位基因(p = 0.010)之间存在关联。我们还对75个家庭成员的基因组DNA可用于HLA分型的家庭进行了连锁分析。该分析结果支持AA与II类基因座之间的连锁关系,在5%重组率时与HLA - DQB的最大LOD得分为2.42,在0%重组率时与HLA - DR的最大LOD得分为2.34。这些家庭中特应性皮炎和自身免疫性甲状腺炎的发病率增加。AA似乎是一种II类HLA限制的针对毛囊的器官特异性免疫反应。

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