Differential display analysis of murine encephalitogenic mRNA

被引:2
作者
Jeong, MC
Izikson, L
Uccelli, A
Brocke, S
Oksenberg, JR
机构
[1] Univ Calif San Francisco, Sch Med, Dept Neurol, San Francisco, CA 94143 USA
[2] NINDS, Neurol Dis Sect, NIB, NIH, Bethesda, MD 20892 USA
[3] Univ Genoa, Dept Neurol Sci, I-16132 Genoa, Italy
关键词
autoimmunity; central nervous system; experimental allergic encephalomyelitis; IL-3;
D O I
10.1093/intimm/10.12.1819
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Experimental autoimmune encephalomyelitis (EAE) is an inflammatory demyelinating disease which can be induced by inoculation with activated CD4(+) T lymphocytes specific for myelin proteins. It has been postulated that autoreactive T(h)1-type CD4(+) cells are responsible for the lesions, whereas autoreactive T(h)2-type cells suppress or modulate the disease. However, the mechanisms involved in the development of inflammatory lesions and neurologic deficits in EAE have not been fully described, and probably involve a complex array of mediators and alternative or redundant pathways. To identify additional factors associated with the pathological role of T cells in EAE, we adapted the differential mRNA display technique to fingerprint the transcripts expressed by encephalitogenic and non-encephalitogenic T cells. Using 60 primer combinations, 21 differentially expressed cDNAs were identified. Among them 13 are known sequences, including IL-3 in non-encephalitogenic lymphocytes. Their relevance for the disease process is discussed.
引用
收藏
页码:1819 / 1823
页数:5
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