Ellsworth Jeff L, O'Callaghan Michael, Rubin Hillard, Seymour Albert
Homology Medicines, Inc. , Bedford, Massachusetts.
Hum Gene Ther Clin Dev. 2018 Mar;29(1):60-67. doi: 10.1089/humc.2017.239.
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.
为了评估最近描述的两种F亚群腺相关病毒(AAV)——AAVHSC15和AAVHSC17的治疗效用,在一个具有代表性的人群中评估了针对这些AAV的中和抗体(NAb)的血清流行率,并与AAV9的血清流行率进行比较。在美国收集了100份不同种族(34名黑人、33名白种人和33名西班牙裔)和性别的独特人类血清(49%为女性,51%为男性),并测量了其中的NAb水平。分别用包装有LacZ上游的CMV启动子或萤火虫荧光素酶上游的CBA启动子的载体,在Huh7细胞中检测了56份血清,在2V6.11细胞中检测了44份血清。对于AAVHSC15、AAVHSC17和AAV9,在所有检测的血清中,分别有24/100(24%)、21/100(21%)和17/100(17%)的血清在血清稀释1/16时对细胞转导的抑制率为50%时NAb呈血清阳性,以此作为血清阳性的临界值。只有6%的阳性血清滴度为1/150至1/340,这表明大多数阳性血清的滴度较低。观察到所有三种AAV血清型之间的NAb存在显著的交叉反应性。这些数据表明,在所评估的人群中,约80%的人针对所检测的AAV血清型不存在预先存在的NAb,这表明绝大多数人类受试者适合接受F亚群AAV的治疗干预。