Jeff L Ellsworth, Michael O'Callaghan, Hillard Rubin, Albert Seymour
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引用次数: 9
摘要
为了评估最近描述的两种进化枝F腺相关病毒(aav) AAVHSC15和AAVHSC17的治疗效用,在代表性人群中评估了这些aav的中和抗体(nab)的血清流行率,并与AAV9进行了比较。在美国收集的100种不同种族(34种,黑人,33种高加索人和33种西班牙人)和性别(49%女性,51%男性)的独特人类血清中测量了NAb水平。56份血清在Huh7细胞中检测,44份血清在2V6.11细胞中检测,载体分别包装了LacZ上游的cmv启动子或萤火虫荧光素酶上游的cba启动子。对于AAVHSC15、AAVHSC17和AAV9,分别有24/100(24%)、21/100(21%)和17/100(17%)的血清检测nab血清阳性,在1/16稀释的血清中抑制50%的细胞转导作为血清阳性的切断。只有6%的阳性血清滴度为1/150 ~ 1/340,表明大多数阳性血清滴度较低。nab在所有三种AAV血清型中观察到显著的交叉反应性。这些数据表明,大约80%的被评估人对AAV血清型预先存在的nab呈阴性,这表明绝大多数被评估人可以接受Clade F AAV的治疗干预。
Low Seroprevalence of Neutralizing Antibodies Targeting Two Clade F AAV in Humans.
To assess the therapeutic utility of AAVHSC15 and AAVHSC17, two recently described Clade F adeno-associated viruses (AAVs), the seroprevalence of neutralizing antibodies (NAbs) to these AAVs was assessed in a representative human population and compared to that of AAV9. NAb levels were measured in 100 unique human sera of different races (34, Black, 33 Caucasian, and 33 Hispanic) and sex (49% female, 51% male) collected within the United States. Fifty-six sera were tested in Huh7 cells and 44 sera were tested in 2V6.11 cells with vectors packaged with either a CMV-promoter upstream of LacZ or a CBA-promoter upstream of Firefly Luciferase, respectively. For AAVHSC15, AAVHSC17, and AAV9, 24/100 (24%), 21/100 (21%), and 17/100 (17%), respectively, of all sera tested were seropositive for NAbs using 50% inhibition of cellular transduction at a 1/16 dilution of serum as cutoff for seropositivity. Only 6% of positive sera had titers of 1/150 to 1/340, indicating that the majority of positive sera were of low titer. Significant cross-reactivity of NAbs across all three AAV serotypes was observed. These data show that approximately 80% of humans evaluated were seronegative for pre-existing NAbs to the AAV serotypes tested, suggesting that the vast majority of human subjects would be amenable to therapeutic intervention with Clade F AAVs.
期刊介绍:
Human Gene Therapy (HGT) is the premier, multidisciplinary journal covering all aspects of gene therapy. The Journal publishes important advances in DNA, RNA, cell and immune therapies, validating the latest advances in research and new technologies.