Alector, Inc., South San Francisco, CA, 94080, USA.
Leal Therapeutics, Worcester, MA, USA.
Alzheimers Res Ther. 2024 Oct 23;16(1):235. doi: 10.1186/s13195-024-01599-1.
Variants of the gene triggering receptor expressed on myeloid cells-2 (TREM2) increase the risk of Alzheimer's disease (AD) and other neurodegenerative disorders. Signaling by TREM2, an innate immune receptor expressed by microglia, is thought to enhance phagocytosis of amyloid beta (Aβ) and other damaged proteins, promote microglial proliferation, migration, and survival, and regulate inflammatory signaling. Thus, TREM2 activation has potential to alter the progression of AD. AL002 is an investigational, engineered, humanized monoclonal immunoglobulin G1 (IgG1) antibody designed to target TREM2. In AD mouse models, an AL002 murine variant has been previously shown to induce microglial proliferation and reduce filamentous Aβ plaques and neurite dystrophy.
Preclinical studies assessed the safety, tolerability, pharmacokinetics, and pharmacodynamics of AL002 in cynomolgus monkeys. INVOKE-1 (NCT03635047) was a first-in-human phase 1, randomized, placebo-controlled, double-blind study assessing the safety, tolerability, PK, and PD of AL002 administered as single ascending doses (SAD) in healthy volunteers.
In cynomolgus monkeys, weekly intravenous injections of AL002 for 4 weeks were well tolerated, dose-dependently decreased soluble TREM2 (sTREM2) in cerebrospinal fluid (CSF) and total TREM2 in hippocampus and frontal cortex, and increased biomarkers of TREM2 signaling in CSF and brain. In the phase 1 study of 64 healthy volunteers, a single intravenous infusion of AL002 demonstrated brain target engagement based on a dose-dependent reduction of sTREM2 in CSF and parallel increases in biomarkers of TREM2 signaling and microglia recruitment. Single-dose AL002 showed central nervous system penetrance and was well tolerated, with no treatment-related serious adverse events over 12 weeks.
These findings support the continued clinical development of AL002 for AD and other neurodegenerative diseases in which TREM2 activation may be beneficial. AL002 is currently being tested in a phase 2, randomized, double-blind, placebo-controlled study in early AD.
Clinicaltrials.gov, NCT03635047. Registered on August 15, 2018, https://www.
gov/study/NCT03635047 .
触发髓细胞表达的受体-2(TREM2)基因变异增加了阿尔茨海默病(AD)和其他神经退行性疾病的风险。TREM2 是一种先天免疫受体,由小胶质细胞表达,其信号被认为增强了对淀粉样β(Aβ)和其他受损蛋白的吞噬作用,促进小胶质细胞增殖、迁移和存活,并调节炎症信号。因此,TREM2 的激活有可能改变 AD 的进展。AL002 是一种研究性的、工程化的、人源化的单克隆免疫球蛋白 G1(IgG1)抗体,旨在靶向 TREM2。在 AD 小鼠模型中,先前已经表明 AL002 的鼠变体可诱导小胶质细胞增殖,减少丝状 Aβ斑块和神经突营养不良。
在食蟹猴中进行了评估 AL002 安全性、耐受性、药代动力学和药效学的临床前研究。INVOKE-1(NCT03635047)是一项首次人体的 1 期、随机、安慰剂对照、双盲研究,评估了在健康志愿者中作为单递增剂量(SAD)给予 AL002 的安全性、耐受性、PK 和 PD。
在食蟹猴中,每周静脉注射 AL002 4 周,耐受性良好,剂量依赖性降低脑脊液(CSF)中的可溶性 TREM2(sTREM2)和海马和额叶皮质中的总 TREM2,并增加 CSF 和大脑中 TREM2 信号的生物标志物。在 64 名健康志愿者的 1 期研究中,单次静脉输注 AL002 基于 CSF 中 sTREM2 的剂量依赖性降低和 TREM2 信号和小胶质细胞募集的生物标志物的平行增加,显示出脑靶标结合。单次剂量的 AL002 显示出中枢神经系统穿透力,耐受性良好,在 12 周内无与治疗相关的严重不良事件。
这些发现支持继续开发 AL002 用于 AD 和其他神经退行性疾病,其中 TREM2 激活可能有益。AL002 目前正在早期 AD 的一项 2 期、随机、双盲、安慰剂对照研究中进行测试。
Clinicaltrials.gov,NCT03635047。于 2018 年 8 月 15 日注册,https://www.clinicaltrials.gov/study/NCT03635047。
NCT03635047。