Liu YuTing, Yang Minhua, Fraser Kyle, Graham Danielle, Weinreb Paul H, Weihofen Andreas, Hirst Warren D, Cedarbaum Jesse M, Pepinsky Blake
Biogen, Cambridge, Massachusetts.
Biogen, Cambridge, Massachusetts.
J Pharmacol Exp Ther. 2025 Jan;392(1):100003. doi: 10.1124/jpet.124.002199. Epub 2024 Nov 22.
Through its pathological and genetic association with Parkinson disease (PD), α-synuclein (α-syn) remains a favorable therapeutic target that is being investigated using various modalities, including many passive immunotherapy approaches clinically targeting different forms of α-syn and epitopes. Although published studies from some immunotherapy trials have demonstrated engagement in plasma, none has shown direct drug-antigen interactions in the disease-relevant compartment, the central nervous system. Cinpanemab (BIIB054) selectively targets pathological aggregated α-syn with low-affinity binding to monomeric forms. The avidity-driven binding, low drug concentration, and the very low α-syn levels, plus its heterogeneous nature in cerebrospinal fluid (CSF), made it impossible to measure drug-target interactions by conventional assays. Here we overcame these challenges by using zero-length crosslinking to stabilize the BIIB054-α-syn complexes and then quantified the crosslinked complexes using a Meso Scale Discovery electrochemiluminescence assay. CSF samples from healthy volunteers (HVs, n = 46) and individuals with PD (PD, n = 18) from study 228HV101 (phase 1 clinical trial of BIIB054) demonstrated dose- and time-dependent binding of cinpanemab to α-syn with measurable complexes detected at doses ≥15 mg/kg. Complex formation displayed a direct positive correlation to drug concentration (Spearman rank correlation = 0.8295 [HV], 0.8032 [PD] P < .0001 [HV, PD]). The observed binding of cinpanemab to α-syn in CSF is consistent with its low intrinsic affinity for α-syn monomer and provides evidence that the drug is behaving with expected binding dynamics in the central nervous system compartment. SIGNIFICANCE STATEMENT: A zero-length crosslinking method with Meso Scale Discovery detection was developed to enable quantification of cinpanemab-α-synuclein (α-syn) complexes in clinical cerebrospinal fluid samples by preventing signal loss caused by their rapid dissociation. Observed dose- and time-dependent binding was consistent with cinpanemab's affinity for α-syn and provided confidence the drug had engaged its target at the desired site of action. This is the first demonstration of α-syn binding by an antibody in clinical samples from the central nervous system.
由于其与帕金森病(PD)的病理和遗传关联,α-突触核蛋白(α-syn)仍然是一个理想的治疗靶点,目前正在通过各种方式进行研究,包括许多临床上针对不同形式的α-syn和表位的被动免疫疗法。尽管一些免疫疗法试验的已发表研究表明药物与血浆有相互作用,但没有一项研究显示在疾病相关部位即中枢神经系统中有直接的药物-抗原相互作用。Cinpanemab(BIIB054)选择性地靶向病理性聚集的α-syn,与单体形式的亲和力较低。亲和力驱动的结合、低药物浓度以及极低的α-syn水平,再加上其在脑脊液(CSF)中的异质性,使得无法通过传统检测方法测量药物-靶点相互作用。在这里,我们通过使用零长度交联来稳定BIIB054-α-syn复合物,然后使用Meso Scale Discovery电化学发光检测法对交联复合物进行定量,克服了这些挑战。来自研究228HV101(BIIB054的1期临床试验)的健康志愿者(HV,n = 46)和帕金森病患者(PD,n = 18)的脑脊液样本显示,cinpanemab与α-syn的结合呈剂量和时间依赖性,在剂量≥15 mg/kg时可检测到可测量的复合物。复合物的形成与药物浓度呈直接正相关(斯皮尔曼等级相关系数= 0.8295 [HV],0.8032 [PD],P <.0001 [HV,PD])。在脑脊液中观察到的cinpanemab与α-syn的结合与其对α-syn单体的低内在亲和力一致,并提供了证据表明该药物在中枢神经系统部位表现出预期的结合动力学。意义声明:开发了一种采用Meso Scale Discovery检测的零长度交联方法,可以通过防止因快速解离导致的信号损失来定量临床脑脊液样本中的cinpanemab-α-突触核蛋白(α-syn)复合物。观察到的剂量和时间依赖性结合与cinpanemab对α-syn的亲和力一致,并让人相信该药物已在所需作用部位与靶点结合。这是首次在中枢神经系统的临床样本中证明抗体与α-syn的结合。