Wang Dan, Zhong Li, Li Mengxin, Li Jia, Tran Karen, Ren Lingzhi, He Ran, Xie Jun, Moser Richard P, Fraser Cara, Kuchel Tim, Sena-Esteves Miguel, Flotte Terence R, Aronin Neil, Gao Guangping
Horae Gene Therapy Center, University of Massachusetts Medical School, Worcester, MA 01605, USA.
Li Weibo Institute for Rare Diseases Research, University of Massachusetts Medical School, Worcester, MA 01605, USA.
Mol Ther Methods Clin Dev. 2018 Oct 4;11:65-72. doi: 10.1016/j.omtm.2018.09.003. eCollection 2018 Dec 14.
Pre-existing neutralizing antibody (NAb) against adeno-associated virus (AAV) commonly found in primates is a major host barrier that can severely compromise gene transfer by AAV vectors. To achieve proof-of-concept success in clinical development of recombinant AAV (rAAV)-based gene therapy, it is crucial to consider the potential interference of NAb and to enroll serologically compatible study subjects. In this study, we report a large AAV NAb dataset comprising multiple large animal species and AAV serotypes and compare two NAb assays based on or transduction inhibition, respectively. Together with previously published AAV seroepidemiology studies, these data can serve as a reference for selecting suitable serotypes, study subjects of large animal species, and potentially human patients for rAAV treatment. In addition, we modeled the intrathalamus rAAV9 delivery in the presence of circulating anti-AAV9 NAb generated by either pre-immunization or passive transfer of NAb-positive large animal serum to mice. The data showed that circulating NAb may not be the sole determinant to inhibit brain transduction. Other aspects of pre-existing AAV immunity following natural infection or rAAV administration may be further studied to establish a more accurate inclusion criterion for clinical studies employing intraparenchymal rAAV9 injections.
在灵长类动物中常见的针对腺相关病毒(AAV)的预先存在的中和抗体(NAb)是一个主要的宿主障碍,它会严重损害AAV载体的基因转移。为了在基于重组AAV(rAAV)的基因治疗的临床开发中取得概念验证的成功,考虑NAb的潜在干扰并招募血清学相容的研究对象至关重要。在本研究中,我们报告了一个包含多个大型动物物种和AAV血清型的大型AAV NAb数据集,并分别比较了基于感染或转导抑制的两种NAb检测方法。连同先前发表的AAV血清流行病学研究,这些数据可作为选择合适的血清型、大型动物物种的研究对象以及潜在的接受rAAV治疗的人类患者的参考。此外,我们模拟了在通过预先免疫或向小鼠被动转移NAb阳性大型动物血清而产生循环抗AAV9 NAb的情况下,向丘脑内递送rAAV9。数据表明,循环NAb可能不是抑制脑转导的唯一决定因素。对于采用脑实质内注射rAAV9的临床研究,可能需要进一步研究自然感染或给予rAAV后预先存在的AAV免疫的其他方面,以建立更准确的纳入标准。