Corzo D, Yunis J J, Yunis E J, Howard A, Lieberman J A
Dana-Farber Cancer Institute, Department of Pathology, Harvard Medical School, Boston, Mass 02115.
J Clin Psychiatry. 1994 Sep;55 Suppl B:149-52.
In order to extend the analysis of the association between class I and class II HLA markers and HSP-70 alleles, we studied the genetic polymorphism of HSP70-2 genes by restriction fragment length polymorphism analysis in a panel of HLA-homozygous cell lines carrying the HLA-B alleles known to be associated with clozapine-induced agranulocytosis. We have found a linkage disequilibrium between the 9.0 kb variant of HSP70-2 with the class I antigens HLA-B7, B38, and B44 and with the class II antigens HLA-DR2 and DR4. We discuss the importance of analyzing the variants of HSP70-2 in patients with agranulocytosis to confirm that the 9.0 kb allele is a genetic marker for the disease. If that is the case, HSP-70 variants could explain the different associations of HLA alleles in individuals of Jewish and non-Jewish ancestry because the HLA alleles are in linkage disequilibrium with the 9.0 kb band. We postulate that HSP-70 molecules could also play a significant role in determining the molecular mechanisms that induce agranulocytosis by clozapine.
为了扩展对I类和II类HLA标记与HSP - 70等位基因之间关联的分析,我们通过限制性片段长度多态性分析,在一组携带已知与氯氮平诱导的粒细胞缺乏症相关的HLA - B等位基因的HLA纯合细胞系中,研究了HSP70 - 2基因的遗传多态性。我们发现HSP70 - 2的9.0 kb变体与I类抗原HLA - B7、B38和B44以及与II类抗原HLA - DR2和DR4之间存在连锁不平衡。我们讨论了分析粒细胞缺乏症患者中HSP70 - 2变体以确认9.0 kb等位基因是该疾病遗传标记的重要性。如果是这样,HSP - 70变体可以解释犹太和非犹太血统个体中HLA等位基因的不同关联,因为HLA等位基因与9.0 kb条带存在连锁不平衡。我们推测HSP - 70分子在确定氯氮平诱导粒细胞缺乏症的分子机制中也可能起重要作用。