Ross C J, Bastedo L, Maier S A, Sands M S, Chang P L
Department of Biology, McMaster University, Hamilton, Ontario, L8N 3Z5 Canada.
Hum Gene Ther. 2000 Oct 10;11(15):2117-27. doi: 10.1089/104303400750001426.
Most lysosomal enzyme deficiencies are catastrophic illnesses with no generally available treatments. We have used the beta-glucuronidase-deficient mouse model of mucopolysaccharidosis type VII (MPS VII) to develop an alternative approach to therapy. A "universal" cell line engineered to secrete the missing enzyme is implanted in all recipients requiring the same enzyme replacement. The cells, although nonautologous, are rendered immunologically tolerant by encapsulation in microcapsules that provide protection from immune mediators. Using this strategy, we injected beta-glucuronidase-secreting fibroblasts enclosed in alginate microcapsules into mutant MPS VII mice. After 24 hr, beta-glucuronidase activity was detected in the plasma, reaching 66% of physiological levels by 2 weeks postimplantation. Significant beta-glucuronidase activity was detected in liver and spleen for the duration of the 8-week experiment. Concomitantly, the intralysosomal accumulation of undegraded glycosaminoglycans was dramatically reduced in liver and spleen tissue sections and urinary glycosaminoglycan content was reduced to normal levels. Elevated secondary lysosomal enzymes beta-hexosaminidase and alpha-galactosidase were also reduced. However, implanted mutant MPS VII mice developed antibodies against the murine beta-glucuronidase, demonstrating a potential obstacle in patients with a null mutation who react against the replaced enzyme as a foreign antigen. The antibody response was transiently circumvented with a single treatment of purified anti-CD4 antibody coadministered with the microcapsules. This resulted in increased levels and duration of beta-glucuronidase delivery. Similarly, treated heterozygous mice maintained elevated levels of beta-glucuronidase and did not develop antibodies. This novel cell-based therapy demonstrates a potentially cost-effective and nonviral treatment applicable to all lysosomal storage diseases.
大多数溶酶体酶缺乏症都是灾难性疾病,目前尚无普遍可用的治疗方法。我们利用黏多糖贮积症VII型(MPS VII)的β-葡萄糖醛酸酶缺陷小鼠模型开发了一种替代治疗方法。一种经过基因工程改造以分泌缺失酶的“通用”细胞系被植入所有需要相同酶替代治疗的受体体内。这些细胞虽然不是自体的,但通过包裹在微胶囊中实现免疫耐受,微胶囊可保护细胞免受免疫介质的影响。采用这种策略,我们将包裹在藻酸盐微胶囊中的分泌β-葡萄糖醛酸酶的成纤维细胞注射到突变型MPS VII小鼠体内。24小时后,在血浆中检测到β-葡萄糖醛酸酶活性,植入后2周达到生理水平的66%。在为期8周的实验期间,在肝脏和脾脏中均检测到显著的β-葡萄糖醛酸酶活性。同时,肝脏和脾脏组织切片中未降解糖胺聚糖的溶酶体内积累显著减少,尿糖胺聚糖含量降至正常水平。升高的次级溶酶体酶β-己糖胺酶和α-半乳糖苷酶也有所降低。然而,植入的突变型MPS VII小鼠产生了针对小鼠β-葡萄糖醛酸酶的抗体,这表明对于那些将替代酶作为外来抗原产生反应的无义突变患者存在潜在障碍。通过与微胶囊共同施用一次纯化的抗CD4抗体,可暂时规避抗体反应。这导致β-葡萄糖醛酸酶递送水平提高且持续时间延长。同样,经治疗的杂合小鼠维持了较高水平的β-葡萄糖醛酸酶且未产生抗体。这种基于细胞的新型疗法证明了一种潜在的具有成本效益且非病毒的治疗方法,适用于所有溶酶体贮积症。