MHC typing in variant Creutzfeldt-Jakob disease

被引:19
作者
Pepys, MB
Bybee, A
Booth, DR
Bishop, MT
Will, RG
Little, AM
Prokupek, B
Madrigal, JA
机构
[1] UCL Royal Free & Univ Coll Med Sch, Dept Med, Ctr Amyloidosis & Acute Phase Prot, London NW3 2PF, England
[2] Univ Edinburgh, Western Gen Hosp, Natl CJD Surveillance Unit, Edinburgh, Midlothian, Scotland
[3] UCL Royal Free Hosp, Anthony Nolan Res Inst & Histocompatibil Labs, London NW3 2QG, England
基金
英国医学研究理事会;
关键词
D O I
10.1016/S0140-6736(03)12455-5
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Identification of factors that cause susceptibility to, and clinical expression of, variant Creutzfeldt-Jakob disease (vCJD) is essential for future management of the disease. We established MHC genotypes of 76 individuals with vCJD and 131 controls, and analysed MHC phenotypes in relation to age of onset of vCJD and its duration from presentation to death. There were no significant differences between vCJD and control populations in frequencies of any MHC types, nor were there associations between MHC type and age of onset or duration of vCJD disease. Our results do not support the idea of an association between MHC types and either susceptibility to, or expression of, vCJD.
引用
收藏
页码:487 / 489
页数:3
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