Lebon P, Daveau M, Sesboüe R, Ponsot G, Reinert P, Salier J P
INSERM U-43, Hôpital Saint Vincent-de-Paul, Paris, France.
Exp Clin Immunogenet. 1987;4(3):125-8.
Gm phenotype or haplotype frequencies are known to be increased in some neurological diseases involving dysregulation(s) of the immune system. Therefore, possible associations between acute measles encephalitis (AME) or subacute sclerosing panencephalitis (SSPE) and alleles of the Gm system were investigated by comparison of children (41 AME subjects and 62 SSPE subjects) with 378 ethnically and geographically matched controls. Although the Gm3;..;11 haplotype displayed a very low frequency among SSPE children, no statistically significant departure in the distribution of Gm phenotypes could be evidenced between AME or SSPE, and controls. A further appraisal of combined Gm and HLA phenotypes may be warranted in both diseases since Gm/HLA interactions have been demonstrated in other immunopathological conditions.
已知在一些涉及免疫系统失调的神经疾病中,Gm表型或单倍型频率会增加。因此,通过将儿童(41例急性麻疹脑炎患者和62例亚急性硬化性全脑炎患者)与378名种族和地理匹配的对照进行比较,研究了急性麻疹脑炎(AME)或亚急性硬化性全脑炎(SSPE)与Gm系统等位基因之间的可能关联。尽管Gm3;..;11单倍型在SSPE儿童中频率极低,但AME或SSPE患者与对照之间在Gm表型分布上未发现有统计学意义的差异。由于在其他免疫病理状况中已证实存在Gm/HLA相互作用,因此对这两种疾病联合的Gm和HLA表型进行进一步评估可能是必要的。