不利影响
医学
临床终点
免疫原性
内科学
肾上腺脑白质营养不良
胃肠病学
临床试验
药理学
免疫学
抗体
过氧化物酶体
受体
作者
Qiuhong Wang,Jing Wang,Zhipei Ling,Zhiqiang Cui,Jie Gong,Rui Zhang,Shijun Li,Yangyang Wang,Rui Yang,Dehui Huang,Wen He,Jing Gao,Feng Chen,Pei-Li Hu,Liying Liu,Lung‐Ji Chang,Li‐Ping Zou
标识
DOI:10.1016/j.scib.2024.04.072
摘要
This was a single-arm, multicenter, open-label phase I trial. Lentiviral vectors (LV) carrying the ABCD1 gene (LV-ABCD1) was directly injected into the brain of patients with childhood cerebral adrenoleukodystrophy (CCALD), and multi-site injection was performed. The injection dose increased from 200 μL to 1600 μL (vector titer: 1×109 TU/mL), and the average dose per kilogram body weight ranges from 8 μL/kg to 63.6 μL/kg. The primary endpoint was safety, dose‐exploration and immunogenicity and the secondary endpoint was initial evaluation of efficacy and the expression of ABCD1 protein. A total of 7 patients participated in this phase I study and were followed for 1 year. No injection-related serious adverse event or death occurred. Common adverse events associated with the injection were irritability (71%, 5/7) and fever (37.2–38.5 ℃, 57%, 4/7). Adverse events were mild and self-limited, or resolved within 3 days of symptomatic treatment. The maximal tolerable dose is 1600 μL. In 5 cases (83.3%, 5/6), no lentivirus associated antibodies were detected. The overall survival at 1-year was 100%. The ABCD1 protein expression was detected in neutrophils, monocytes and lymphocytes. This study suggests that the intracerebral injection of LV-ABCD1 for CCALD is safe and can achieve successful LV transduction in vivo; even the maximal dose did not increase the risk of adverse events. Furthermore, the direct LV-ABCD1 injection displayed low immunogenicity. In addition, the effectiveness of intracerebral LV-ABCD1 injection has been preliminarily demonstrated while further investigation is needed. This study has been registered in the Chinese Clinical Trial Registry (https://www.chictr.org.cn/, registration number: ChiCTR1900026649).
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