Department of Haematology, University College London Cancer Institute, London, United Kingdom.
N Engl J Med. 2011 Dec 22;365(25):2357-65. doi: 10.1056/NEJMoa1108046. Epub 2011 Dec 10.
Hemophilia B, an X-linked disorder, is ideally suited for gene therapy. We investigated the use of a new gene therapy in patients with the disorder.
We infused a single dose of a serotype-8-pseudotyped, self-complementary adenovirus-associated virus (AAV) vector expressing a codon-optimized human factor IX (FIX) transgene (scAAV2/8-LP1-hFIXco) in a peripheral vein in six patients with severe hemophilia B (FIX activity, <1% of normal values). Study participants were enrolled sequentially in one of three cohorts (given a high, intermediate, or low dose of vector), with two participants in each group. Vector was administered without immunosuppressive therapy, and participants were followed for 6 to 16 months.
AAV-mediated expression of FIX at 2 to 11% of normal levels was observed in all participants. Four of the six discontinued FIX prophylaxis and remained free of spontaneous hemorrhage; in the other two, the interval between prophylactic injections was increased. Of the two participants who received the high dose of vector, one had a transient, asymptomatic elevation of serum aminotransferase levels, which was associated with the detection of AAV8-capsid-specific T cells in the peripheral blood; the other had a slight increase in liver-enzyme levels, the cause of which was less clear. Each of these two participants received a short course of glucocorticoid therapy, which rapidly normalized aminotransferase levels and maintained FIX levels in the range of 3 to 11% of normal values.
Peripheral-vein infusion of scAAV2/8-LP1-hFIXco resulted in FIX transgene expression at levels sufficient to improve the bleeding phenotype, with few side effects. Although immune-mediated clearance of AAV-transduced hepatocytes remains a concern, this process may be controlled with a short course of glucocorticoids without loss of transgene expression. (Funded by the Medical Research Council and others; ClinicalTrials.gov number, NCT00979238.).
血友病 B 是一种 X 连锁疾病,非常适合基因治疗。我们研究了一种新的基因治疗方法在这种疾病患者中的应用。
我们在 6 名严重血友病 B 患者(FIX 活性<正常水平的 1%)外周静脉单次输注一种新型血清型 8 型假型、自我互补腺相关病毒(AAV)载体,表达优化密码子的人因子 IX(FIX)转基因(scAAV2/8-LP1-hFIXco)。研究参与者按顺序分为三个队列中的一个(接受高、中或低剂量的载体),每组 2 人。载体未给予免疫抑制治疗,参与者随访 6 至 16 个月。
所有参与者均观察到 AAV 介导的 FIX 表达水平为正常水平的 2%至 11%。6 名参与者中的 4 名停止了 FIX 预防性治疗且无自发性出血;另外 2 名患者增加了预防性注射的间隔。在接受高剂量载体的 2 名参与者中,1 名患者出现短暂、无症状的血清转氨酶水平升高,这与外周血中检测到 AAV8 衣壳特异性 T 细胞有关;另一名患者的肝酶水平略有升高,其原因不太清楚。这两名参与者均接受了短期糖皮质激素治疗,迅速使转氨酶水平正常化,并使 FIX 水平维持在正常水平的 3%至 11%之间。
scAAV2/8-LP1-hFIXco 通过外周静脉输注可导致 FIX 转基因表达水平足以改善出血表型,且副作用较少。尽管免疫介导的 AAV 转导肝细胞清除仍然是一个问题,但这个过程可以通过短期糖皮质激素治疗来控制,而不会导致转基因表达丧失。(由医学研究委员会和其他机构资助;ClinicalTrials.gov 编号,NCT00979238)。