Human leukocyte antigens and cytokine expression in cerebral inflammatory demyelinative lesions of X-linked adrenoleukodystrophy and multiple sclerosis

被引:77
作者
McGuinness, MC
Powers, JM
Bias, WB
Schmeckpeper, BJ
Segal, AH
Gowda, VC
Wesselingh, SL
Berger, J
Griffin, DE
Smith, KD
机构
[1] JOHNS HOPKINS UNIV,SCH MED,DEPT NEUROL,BALTIMORE,MD 21287
[2] UNIV ROCHESTER,MED CTR,DEPT PATHOL & LAB MED,ROCHESTER,NY 14642
[3] JOHNS HOPKINS UNIV,SCH MED,DEPT MED,BALTIMORE,MD 21287
[4] UNIV VIENNA,INST NEUROL,VIENNA,AUSTRIA
[5] JOHNS HOPKINS UNIV,SCH MED,DEPT PEDIAT,BALTIMORE,MD 21287
关键词
X-linked adrenoleukodystrophy; multiple sclerosis; human leukocyte antigens; cytokines; tumor necrosis factor-alpha;
D O I
10.1016/S0165-5728(97)00020-9
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The two most common forms of X-linked adrenoleukodystrophy (X-ALD) are the cerebral forms (CER) with an inflammatory demyelinating reaction that resembles multiple sclerosis, and adrenomyeloneuropathy (AMN) which involves primarily the spinal cord and in which the inflammatory reaction is mild or absent. We found no significant association between the childhood cerebral farm (CCER) or AMN and the human leukocyte (HLA) class I and class II antigens including the class II DR2 haplotypes associated with multiple sclerosis. Inflammatory cytokine (tumor necrosis facror-alpha, interleukin-1 beta, interleukin-4, interleukin-6 and interferon-gamma) gene expression was increased in multiple sclerosis brain lesions, as has been reported previously, but much less so in CER brain lesions, These findings suggest that the pathogenesis of the inflammatory response in X-ALD differs from that in multiple sclerosis.
引用
收藏
页码:174 / 182
页数:9
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