医学
耐受性
腺相关病毒
不利影响
关节炎
内科学
免疫学
抗体
效价
重组DNA
载体(分子生物学)
基因
生物
生物化学
作者
J.P.M. Vrouwe,J. J. M. Meulenberg,Naomi B. Klarenbeek,A. Navas-Cañete,M. Reijnierse,G. Ruiterkamp,Lisette Bevaart,R.J.S. Lamers,M. Kloppenburg,Rob G. H. H. Nelissen,T. Huizinga,Jacobus Burggraaf,Ingrid M. C. Kamerling
标识
DOI:10.1016/j.joca.2021.09.013
摘要
Inflammatory hand arthritis (IHA) results in impaired function. Local gene therapy with ART-I02, a recombinant adeno-associated virus (AAV) serotype 5 vector expressing interferon (IFN)-β, under the transcriptional control of nuclear factor κ-B responsive promoter, was preclinically shown to have favorable effects. This study aimed to investigate the safety and tolerability of local gene therapy with ART-I02 in patients with IHA.In this first-in-human, dose-escalating, cohort study, 12 IHA patients were to receive a single intra-articular (IA) injection of ART-I02 ranging 0.3 × 1012-1.2 × 1013 genome copies in an affected hand joint. Adverse events (AEs), routine safety laboratory and the clinical course of disease were periodically evaluated. Baseline- and follow-up contrast enhanced magnetic resonance images (MRIs), shedding of viral vectors in bodily fluids, and AAV5 and IFN-β immune responses were evaluated. A data review committee provided safety recommendations.Four patients were enrolled. Long-lasting local AEs were observed in 3 patients upon IA injection of ART-I02. The AEs were moderate in severity and could be treated conservative. Given the duration of the AEs and their possible or probable relation to ART-I02, no additional patients were enrolled. No systemic treatment emergent AEs were observed. The MRIs reflected the AEs by (peri)arthritis. No T-cell response against AAV5 or IFN-β, nor IFN-β antibodies could be detected. Neutralizing antibody titers against AAV5 raised post-dose.Single IA doses of 0.6 × 1012 or 1.2 × 1012 ART-I02 vector genomes were administered without systemic side effects or serious AEs. However, local tolerability was insufficient for continuation.NCT02727764.
科研通智能强力驱动
Strongly Powered by AbleSci AI