Adeno-associated virus serotype 9 antibody seroprevalence for patients in the United States with spinal muscular atrophy

被引:4
作者
Day, John W. [1 ,10 ]
Mendell, Jerry R. [2 ,3 ,4 ]
Burghes, Arthur H. M. [5 ,6 ]
van Olden, Rudolf W. [7 ]
Adhikary, Rishi R. [8 ]
Dilly, Keith W. [9 ]
机构
[1] Stanford Univ, Med Ctr, Dept Neurol, Stanford, CA USA
[2] Nationwide Childrens Hosp, Ctr Gene Therapy, Columbus, OH USA
[3] Ohio State Univ, Dept Pediat, Columbus, OH USA
[4] Ohio State Univ, Dept Neurol, Columbus, OH USA
[5] Ohio State Univ, Dept Neurol, Columbus, OH USA
[6] Ohio State Univ, Dept Biol Chem & Pharmacol, Columbus, OH USA
[7] Novartis Gene Therapies Switzerland GmbH, Rotkreuz, Switzerland
[8] Novartis Healthcare Pvt Ltd, CONEXTS Real World Evidence, Hyderabad, India
[9] Novartis Gene Therapies Inc, Bannockburn, IL USA
[10] Stanford Univ, Med Ctr, Dept Neurol, MC 5979,213 Quarry Rd, Palo Alto, CA 94304 USA
关键词
NEUTRALIZING ANTIBODIES; IMMUNE-RESPONSES; PREVALENCE; MANAGEMENT; DIAGNOSIS; CHILDREN; THERAPY; PROTEIN; VECTOR; CARE;
D O I
10.1016/j.omtm.2023.101117
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Onasemnogene abeparvovec is a recombinant adeno-associated virus serotype 9 (AAV9) vector-based gene therapy for spinal muscular atrophy (SMA). Patients with elevated titers of anti-AAV9 antibodies (AAV9-Ab) should not receive onasemnogene abeparvovec because of potential safety and efficacy implications. We conducted a retrospective study to describe the seroprevalence of anti-AAV9 binding antibodies for pediatric patients with SMA in the United States. At initial testing, 13.0% (115 of 882) of patients (mean [SD] age, 26.29 [33.66] weeks) had elevated AAV9-Ab titers. The prevalence of elevated titers decreased as age increased, with 18.2% (92 of 507) of patients <= 3 months old but only 1.1% (1 of 92) of patients >= 21 months old having elevated titers. This suggests transplacental maternal transfer of antibodies. No patterns of geographic variations in AAV9-Ab prevalence were confirmed. Elevated AAV9-Ab titers in children <6 weeks old decreased in all circumstances. Lower magnitudes of elevated titers declined more rapidly than greater magnitudes. Retesting was completed at the discretion of the treating clinician, so age at testing and time between tests varied. AAV9-Ab retesting should be considered when patients have elevated titers, and elevations at a young age are not a deterrent to eventual onasemnogene abeparvovec administration. Early disease-modifying treatment for SMA leads to optimal outcomes.
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页数:10
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