Miller T, Bleumink N
Eur J Cancer Clin Oncol. 1984 Oct;20(10):1307-16. doi: 10.1016/0277-5379(84)90260-8.
The recently developed acridine derivative 4'-[(9-acridinyl)amino] methanesulphon-m-anisidine (m-AMSA) has become one of the preferred agents in the management of acute leukaemia but little is known of its effects on cellular immune components. We evaluated the qualitative and quantitative effects of m-AMSA on immune cell numbers and function, during both the leucopenic and myelorestorative phases, following intermittent high-dose therapy. Cell-mediated and inflammatory responses were depressed in the treated animals during the leucopenic phase but restoration of immune capability paralleled the recovery of circulating leucocyte numbers. Additionally, m-AMSA displayed unexpected immunomodulatory features: thymus-dependent antibody and delayed-type hypersensitivity responses were actually increased, suggesting the potential of m-AMSA as an immunoregulator in clinical and experimental studies.
最近研制的吖啶衍生物4'-[(9-吖啶基)氨基]甲磺基间茴香胺(m-AMSA)已成为治疗急性白血病的首选药物之一,但对其对细胞免疫成分的影响却知之甚少。我们评估了间歇性高剂量治疗后,在白细胞减少期和骨髓恢复阶段,m-AMSA对免疫细胞数量和功能的定性和定量影响。在白细胞减少期,治疗动物的细胞介导和炎症反应受到抑制,但免疫能力的恢复与循环白细胞数量的恢复平行。此外,m-AMSA表现出意想不到的免疫调节特性:依赖胸腺的抗体和迟发型超敏反应实际上增强了,这表明m-AMSA在临床和实验研究中作为免疫调节剂的潜力。