Leisegang Rory, Silber Baumann Hanna E, Lennon-Chrimes Siân, Ito Hajime, Miya Kazuhiro, Genin Jean-Christophe, Plan Elodie L
Department of Pharmacy, Uppsala University, Uppsala, Sweden.
Roche Pharma Research and Early Development, Pharmaceutical Sciences, Roche Innovation Center Basel, Basel, Switzerland.
CPT Pharmacometrics Syst Pharmacol. 2024 Dec;13(12):2171-2184. doi: 10.1002/psp4.13230. Epub 2024 Oct 8.
Immunogenicity is the propensity of a therapeutic protein to generate an immune response to itself. While reporting of antidrug antibodies (ADAs) is increasing, model-based analysis of such data is seldom performed. Model-based characterization of factors affecting the emergence and dissipation of ADAs may inform drug development and/or improve understanding in clinical practice. This analysis aimed to predict ADA dynamics, including the potential influence of individual covariates, following subcutaneous satralizumab administration. Satralizumab is a humanized IgG2 monoclonal recycling IL-6 receptor antagonist antibody approved for treating neuromyelitis optica spectrum disorder (NMOSD). Longitudinal pharmacokinetic (PK) and ADA data from 154 NMOSD patients in two pivotal Phase 3 studies (NCT02028884, NCT02073279) and PK data from one Phase 1 study (SA-001JP) in 72 healthy volunteers were available for this analysis. An existing population PK model was adapted to derive steady-state concentration without ADA for each patient. A mixed hidden Markov model (mHMM) was developed whereby three different states were identified: one absorbing Markov state for non-ADA developer, and two dynamic and inter-connected Markov states-transient ADA negative and positive. Satralizumab exposure and body mass index impacted transition probabilities and, therefore, the likelihood of developing ADAs. In conclusion, the mHMM model was able to describe the time course of ADA development and identify patterns of ADA development in NMOSD patients following treatment with satralizumab, which may allow for the formulation of strategies to reduce the emergence or limit the impact of ADA in the clinical setting.
免疫原性是治疗性蛋白质引发自身免疫反应的倾向。虽然抗药物抗体(ADA)的报告日益增多,但对此类数据进行基于模型的分析却很少。基于模型对抗药物抗体出现和消散的影响因素进行特征描述,可能会为药物开发提供信息和/或增进对临床实践的理解。本分析旨在预测皮下注射萨特利珠单抗后抗药物抗体的动态变化,包括个体协变量的潜在影响。萨特利珠单抗是一种人源化IgG2单克隆循环IL-6受体拮抗剂抗体,已被批准用于治疗视神经脊髓炎谱系障碍(NMOSD)。两项关键的3期研究(NCT02028884、NCT02073279)中154例NMOSD患者的纵向药代动力学(PK)和抗药物抗体数据,以及一项1期研究(SA-001JP)中72名健康志愿者的PK数据可用于本分析。采用现有的群体药代动力学模型来推导每位患者无抗药物抗体时的稳态浓度。开发了一种混合隐马尔可夫模型(mHMM),确定了三种不同状态:一种是针对非抗药物抗体产生者的吸收性马尔可夫状态,以及两种动态且相互关联的马尔可夫状态——短暂抗药物抗体阴性和阳性状态。萨特利珠单抗暴露和体重指数影响转变概率,进而影响产生抗药物抗体的可能性。总之,mHMM模型能够描述抗药物抗体产生的时间过程,并识别NMOSD患者接受萨特利珠单抗治疗后抗药物抗体产生的模式,这可能有助于制定策略以减少抗药物抗体在临床环境中的出现或限制其影响。