Laboratory of Molecular Biology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892-4264, USA.
Br J Haematol. 2010 Aug;150(3):352-8. doi: 10.1111/j.1365-2141.2010.08251.x. Epub 2010 Jun 7.
Acute lymphoblastic leukaemia (ALL) remains the most frequent cause of cancer-related mortality in paediatrics and outcome is poor for patients who have high-risk ALL or relapse. HA22 (CAT-8015) is an immunotoxin composed of an anti-CD22 variable fragment linked to a 38 kDa truncated protein derived from Pseudomonas exotoxin A. Using a bone marrow mesenchymal cell culture assay to support ALL cell viability, we investigated the in vitro cytotoxicity of HA22 against ALL blasts from newly diagnosed (n = 13) and relapsed patients (n = 22). There was interpatient variability in sensitivity to HA22. Twenty-four of 35 patient samples tested were sensitive (median 50% lethal concentration 3 ng/ml, range 1-80 ng/ml). Blasts from the other 11 patients were not killed by 500 ng/ml HA22. The median 50% lethal concentration was 20 ng/ml for all patients. There was no significant difference in HA22 sensitivity between diagnosis and relapse samples but peripheral blood ALL blasts were more sensitive to HA22 than those from bone marrow (P = 0.008). Thus, HA22, at concentrations achievable in patients, is highly cytotoxic to B-lineage ALL cells. These results provide a strong rationale for clinical testing of this agent in children with drug-resistant ALL and offers the potential to reduce morbidities of treatment while improving outcome.
急性淋巴细胞白血病(ALL)仍然是儿科癌症相关死亡的最常见原因,对于患有高危 ALL 或复发的患者,其预后仍然较差。HA22(CAT-8015)是一种免疫毒素,由与来自绿脓杆菌外毒素 A 的 38 kDa 截断蛋白连接的抗 CD22 可变片段组成。我们使用骨髓间充质细胞培养测定法来支持 ALL 细胞的存活能力,研究了 HA22 对新诊断(n=13)和复发患者(n=22)ALL blasts 的体外细胞毒性。对 HA22 的敏感性存在个体间差异。在 35 个患者样本中,有 24 个对 HA22 敏感(中位数 50%致死浓度为 3ng/ml,范围为 1-80ng/ml)。另外 11 个患者的blasts 未被 500ng/ml HA22 杀死。所有患者的中位数 50%致死浓度为 20ng/ml。在诊断和复发样本之间,HA22 的敏感性没有差异,但外周血 ALL blasts 比骨髓中的 ALL blasts 对 HA22 更敏感(P=0.008)。因此,HA22 在患者可达到的浓度下对 B 细胞系 ALL 细胞具有高度细胞毒性。这些结果为在耐药性 ALL 儿童中对该药物进行临床测试提供了强有力的理论依据,并提供了在提高疗效的同时减少治疗并发症的潜力。