Department of Pediatrics, University of Florida, Gainesville, Florida, USA.
National Human Genome Research Institute, NIH, Bethesda, Maryland, USA.
J Clin Invest. 2024 Jan 2;134(1):e173510. doi: 10.1172/JCI173510.
BACKGROUNDSystemic administration of adeno-associated virus (AAV) can trigger life-threatening inflammatory responses, including thrombotic microangiopathy (TMA), acute kidney injury due to atypical hemolytic uremic syndrome-like complement activation, immune-mediated myocardial inflammation, and hepatic toxicity.METHODSWe describe the kinetics of immune activation following systemic AAV serotype 9 (AAV9) administration in 38 individuals following 2 distinct prophylactic immunomodulation regimens. Group 1 received corticosteroids and Group 2 received rituximab plus sirolimus in addition to steroids to prevent anti-AAV antibody formation.RESULTSGroup 1 participants had a rapid increase in immunoglobulin M (IgM) and IgG. Increase in D-dimer, decline in platelet count, and complement activation are indicative of TMA. All Group 1 participants demonstrated activation of both classical and alternative complement pathways, as indicated by depleted C4 and elevated soluble C5b-9, Ba, and Bb antigens. Group 2 patients did not have a significant change in IgM or IgG and had minimal complement activation.CONCLUSIONSThis study demonstrates that TMA in the setting of AAV gene therapy is antibody dependent (classical pathway) and amplified by the alternative complement pathway. Critical time points and interventions are identified to allow for management of immune-mediated events that impact the safety and efficacy of systemic gene therapy.
腺相关病毒(AAV)的全身给药会引发危及生命的炎症反应,包括血栓性微血管病(TMA)、补体激活引起的非典型溶血性尿毒症样综合征导致的急性肾损伤、免疫介导的心肌炎症和肝毒性。
我们描述了 38 名个体在接受 2 种不同的预防性免疫调节方案后,全身 AAV 血清型 9(AAV9)给药后免疫激活的动力学。第 1 组接受皮质类固醇治疗,第 2 组接受利妥昔单抗加西罗莫司加皮质类固醇,以防止抗 AAV 抗体形成。
第 1 组参与者的免疫球蛋白 M(IgM)和 IgG 迅速增加。D-二聚体增加、血小板计数下降和补体激活表明存在 TMA。所有第 1 组参与者均表现出经典和替代补体途径的激活,这表明 C4 耗尽和可溶性 C5b-9、Ba 和 Bb 抗原升高。第 2 组患者的 IgM 或 IgG 没有明显变化,补体激活也很少。
本研究表明,AAV 基因治疗中 TMA 是抗体依赖性的(经典途径),并被替代补体途径放大。确定了关键时间点和干预措施,以管理影响全身基因治疗安全性和疗效的免疫介导事件。