A sensitive and drug tolerant assay for detecting anti-AAV9 antibodies using affinity capture elution

抗体 单克隆抗体 分子生物学 重组DNA 生物 亲和层析 病毒学 免疫学 基因 生物化学
作者
Emma Simmons,Yi Wen,Jingling Li,Yuewei Qian,Li Chin Wong,Robert J. Konrad,Nicoletta Bivi
出处
期刊:Journal of Immunological Methods [Elsevier]
卷期号:512: 113397-113397 被引量:6
标识
DOI:10.1016/j.jim.2022.113397
摘要

Adeno-associated virus (AAV) based gene therapies are gaining significant momentum as a novel therapeutic modality. However, a yet unsolved concern for using AAV as a vector is the high potential to elicit humoral and cellular responses, which are often exacerbated by pre-existing immunity due to exposure to wild type AAV. Therefore, characterization of pre-existing and treatment emergent anti-AAV antibodies is of great importance to the development of AAV based gene therapies. In this project, a sensitive and drug tolerant total antibody (TAb) assay was developed using recombinant AAV9-GFP (green fluorescent protein) as a surrogate AAV9. The assay format was affinity capture and elution (ACE) with ruthenium labeled AAV9-GFP as detection. Upon evaluation, three commercial anti-AAV9 monoclonal antibodies (clones HI17, HI35, and HL2374) were chosen and mixed at equal concentrations as positive control material. The assay sensitivity was estimated to be 11.2 ng/mL. Drug tolerance was estimated to be 5.4 × 10E10 DRP/mL AAV9-GFP at 100 ng/mL anti-AAV9 antibodies and to be at least 1 × 10E11 DRP/mL at 500 ng/mL and 250 ng/mL anti-AAV9 antibodies. The assay showed desirable specificity and precision. Using this TAb assay, significant pre-existing antibodies were detected from normal human sera.
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