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危及生命的低磷酸酯酶症的酶替代疗法。

Enzyme-replacement therapy in life-threatening hypophosphatasia.

机构信息

Center for Metabolic Bone Disease and Molecular Research, Shriners Hospital for Children, St. Louis, MO 63131, USA.

出版信息

N Engl J Med. 2012 Mar 8;366(10):904-13. doi: 10.1056/NEJMoa1106173.

Abstract

BACKGROUND

Hypophosphatasia results from mutations in the gene for the tissue-nonspecific isozyme of alkaline phosphatase (TNSALP). Inorganic pyrophosphate accumulates extracellularly, leading to rickets or osteomalacia. Severely affected babies often die from respiratory insufficiency due to progressive chest deformity or have persistent bone disease. There is no approved medical therapy. ENB-0040 is a bone-targeted, recombinant human TNSALP that prevents the manifestations of hypophosphatasia in Tnsalp knockout mice.

METHODS

We enrolled infants and young children with life-threatening or debilitating perinatal or infantile hypophosphatasia in a multinational, open-label study of treatment with ENB-0040. The primary objective was the healing of rickets, as assessed by means of radiographic scales. Motor and cognitive development, respiratory function, and safety were evaluated, as well as the pharmacokinetics and pharmacodynamics of ENB-0040.

RESULTS

Of the 11 patients recruited, 10 completed 6 months of therapy; 9 completed 1 year. Healing of rickets at 6 months in 9 patients was accompanied by improvement in developmental milestones and pulmonary function. Elevated plasma levels of the TNSALP substrates inorganic pyrophosphate and pyridoxal 5'-phosphate diminished. Increases in serum parathyroid hormone accompanied skeletal healing, often necessitating dietary calcium supplementation. There was no evidence of hypocalcemia, ectopic calcification, or definite drug-related serious adverse events. Low titers of anti-ENB-0040 antibodies developed in four patients, with no evident clinical, biochemical, or autoimmune abnormalities at 48 weeks of treatment.

CONCLUSIONS

ENB-0040, an enzyme-replacement therapy, was associated with improved findings on skeletal radiographs and improved pulmonary and physical function in infants and young children with life-threatening hypophosphatasia. (Funded by Enobia Pharma and Shriners Hospitals for Children; ClinicalTrials.gov number, NCT00744042.).

摘要

背景

低磷酸酶血症是由于组织非特异性碱性磷酸酶(TNSALP)基因的突变引起的。无机焦磷酸盐在细胞外积聚,导致佝偻病或骨软化症。严重受影响的婴儿常因进行性胸部畸形导致呼吸衰竭而死亡,或患有持续性骨病。目前尚无批准的医学治疗方法。ENB-0040 是一种针对骨骼的重组人 TNSALP,可预防 Tnsalp 敲除小鼠的低磷酸酶血症表现。

方法

我们招募了患有危及生命或使人衰弱的围产期或婴儿期低磷酸酶血症的婴儿和幼儿,进行了一项关于 ENB-0040 治疗的多国、开放性研究。主要目标是通过放射学量表评估佝偻病的愈合。评估了运动和认知发育、呼吸功能以及 ENB-0040 的药代动力学和药效学。

结果

在招募的 11 名患者中,有 10 名完成了 6 个月的治疗;9 名完成了 1 年的治疗。9 名患者在 6 个月时佝偻病的愈合伴随着发育里程碑和肺功能的改善。升高的 TNSALP 底物无机焦磷酸盐和吡哆醛 5'-磷酸的血浆水平降低。甲状旁腺激素水平的升高伴随着骨骼愈合,通常需要补充膳食钙。没有低钙血症、异位钙化或明确的与药物相关的严重不良事件的证据。四名患者产生了低滴度的抗 ENB-0040 抗体,在治疗 48 周时没有明显的临床、生化或自身免疫异常。

结论

ENB-0040,一种酶替代疗法,与危及生命的低磷酸酶血症婴儿和幼儿骨骼放射照片上的改善发现以及肺部和身体功能的改善相关。(由 Enobia Pharma 和 Shriners Hospitals for Children 资助;ClinicalTrials.gov 编号,NCT00744042。)

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