Loeffler S, Fehsel K, Henning U, Fischer J, Agelink M, Kolb-Bachofen V, Klimke A
Pharmacopsychiatry. 2003 Jan;36(1):37-41. doi: 10.1055/s-2003-38091.
A 45-year-old female suffering from severe chronic schizophrenia of the paranoid type did not respond to typical antipsychotics. Five weeks after starting therapy with clozapine, she developed a clozapine-induced agranulocytosis (CA). Discontinuation of clozapine and treatment with granulocyte colony-stimulating factor (G-CSF) led to normalization of blood neutrophil counts within three weeks. This report suggests enhanced apoptosis of blood neutrophils during the acute phase of CA resulting from enhanced expression of the pro-apoptotic proteins Bax and Bik and from a decrease of the anti-apoptotic BCl-X(L) mRNA. The time course of decline and recovery of neutrophilic cells, as well as the release pattern of endogenous G-CSF, resembles those of chemotherapy-induced neutropenia. The kinetics of CD 34-positive cells mimics that of cytotoxic progenitor cell mobilization, e. g., after cytostatic drug administration. Our findings argue against the hypothesis that clozapine-mediated inhibition of G-CSF or granulocyte-macrophage colony-stimulating factor (GM-CSF) release is involved in CA development. Because clozapine-induced cell death mainly affects the neutrophil lineage, the elucidation of the exact mechanism of CA may open new perspectives for the treatment of psychiatric and possibly hematological disorders.
一名45岁患有严重偏执型慢性精神分裂症的女性对典型抗精神病药物无反应。在开始使用氯氮平治疗五周后,她出现了氯氮平诱导的粒细胞缺乏症(CA)。停用氯氮平并使用粒细胞集落刺激因子(G-CSF)治疗后,血液中性粒细胞计数在三周内恢复正常。本报告表明,在CA急性期,血液中性粒细胞凋亡增强,这是由于促凋亡蛋白Bax和Bik的表达增强以及抗凋亡BCl-X(L) mRNA的减少所致。中性粒细胞的下降和恢复时间进程以及内源性G-CSF的释放模式与化疗诱导的中性粒细胞减少症相似。CD 34阳性细胞的动力学模仿了细胞毒性祖细胞动员的动力学,例如在给予细胞抑制药物后。我们的研究结果反对氯氮平介导的G-CSF或粒细胞-巨噬细胞集落刺激因子(GM-CSF)释放抑制参与CA发生的假说。由于氯氮平诱导的细胞死亡主要影响中性粒细胞谱系,阐明CA的确切机制可能为精神疾病以及可能的血液系统疾病的治疗开辟新的前景。