Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, 46285, Indiana, USA.
AAPS J. 2024 Apr 3;26(3):41. doi: 10.1208/s12248-024-00914-w.
Small interfering RNA (siRNA) is gaining momentum as a therapeutic modality with six approved products. Since siRNA has the potential to elicit undesired immune responses in patients, immunogenicity assessment is required during clinical development by regulatory authorities. In this study, anti-siRNA polyclonal antibodies were generated through animal immunization. These cross-reactive polyclonal antibodies recognized mostly the N-acetylgalactosamine (GalNAc) moiety with a small fraction against sequence-independent epitopes. We demonstrate that the polyclonal antibodies can be utilized as immunogenicity assay positive controls for the same class of GalNAc-conjugated siRNAs. In addition, anti-GalNAc mAbs showed desired sensitivity and drug tolerance, supporting their use as alternative surrogate positive controls. These findings can guide positive control selection and immunogenicity assay development for GalNAc-conjugated siRNAs and other oligonucleotide therapeutics.
小干扰 RNA(siRNA)作为一种治疗模式正在兴起,已有六种产品获得批准。由于 siRNA 有可能在患者中引发不良的免疫反应,因此监管机构在临床开发过程中需要进行免疫原性评估。在这项研究中,通过动物免疫产生了抗 siRNA 多克隆抗体。这些交叉反应的多克隆抗体主要识别 N-乙酰半乳糖胺(GalNAc)部分,一小部分针对序列非依赖性表位。我们证明,多克隆抗体可用作同种 GalNAc 缀合 siRNA 的免疫原性测定阳性对照。此外,抗 GalNAc mAb 表现出理想的灵敏度和药物耐受性,支持将其用作替代替代阳性对照。这些发现可以为 GalNAc 缀合 siRNA 和其他寡核苷酸治疗药物的阳性对照选择和免疫原性测定开发提供指导。