Alzheimer's Research Group, Grifols, Barcelona, Spain.
Alzheimer's Research Group, Grifols, Barcelona, Spain.
Transfus Apher Sci. 2021 Jun;60(3):103164. doi: 10.1016/j.transci.2021.103164. Epub 2021 May 21.
Alzheimer's disease (AD) is a neurodegenerative process that inexorably leads to progressive deterioration of cognition function and, ultimately, death. Central pathophysiologic features of AD include the accumulation of extracellular plaques comprised of amyloid-β peptide (Aβ) and the presence of intraneuronal neurofibrillary tangles. However, a large body of evidence suggests that oxidative stress and inflammation are major contributors to the pathogenesis and progression of AD. To date, available pharmacologic treatments are only symptomatic. Clinical trials focused on amyloid and non-amyloid-targeted treatments with small molecule pharmacotherapy and immunotherapies have accumulated a long list of failures. Considering that around 90 % of the circulating Aβ is bound to albumin, and that a dynamic equilibrium exists between peripheral and central Aβ, plasma exchange with albumin replacement has emerged as a new approach in a multitargeted AD therapeutic strategy (AMBAR Program). In plasma exchange, a patient's plasma is removed by plasmapheresis to eliminate toxic endogenous substances, including Aβ and functionally impaired albumin. The fluid replacement used is therapeutic albumin, which acts not only as a plasma volume expander but also has numerous pleiotropic functions (e.g., circulating Aβ- binding capacity, transporter, detoxifier, antioxidant) that are clinically relevant for the treatment of AD. Positive results from the AMBAR Program (phase 1, 2, an 2b/3 trials), i.e., slower decline or stabilization of disease symptoms in the most relevant clinical efficacy and safety endpoints, offer a glimmer of hope to both AD patients and caregivers.
阿尔茨海默病(AD)是一种神经退行性疾病,它会导致认知功能逐渐恶化,最终导致死亡。AD 的中心病理生理特征包括细胞外斑块的积累,这些斑块由淀粉样β肽(Aβ)组成,以及神经元内神经原纤维缠结的存在。然而,大量证据表明,氧化应激和炎症是 AD 发病机制和进展的主要因素。迄今为止,可用的药物治疗仅为对症治疗。以淀粉样蛋白和非淀粉样蛋白为靶点的小分子药物治疗和免疫疗法的临床试验积累了大量失败。考虑到大约 90%的循环 Aβ与白蛋白结合,并且外周和中枢 Aβ之间存在动态平衡,用白蛋白替代物进行血浆置换已成为一种新的多靶点 AD 治疗策略(AMBAR 计划)。在血浆置换中,通过血浆分离术去除患者的血浆以消除包括 Aβ在内的毒性内源性物质和功能受损的白蛋白。使用的液体替代物是治疗性白蛋白,它不仅作为血浆容量扩张剂,而且具有许多多效性功能(例如,循环 Aβ结合能力、转运蛋白、解毒剂、抗氧化剂),这些功能在 AD 的治疗中具有临床相关性。AMBAR 计划(第 1、2 和 2b/3 期)的积极结果,即最相关的临床疗效和安全性终点疾病症状的下降或稳定,为 AD 患者和护理人员带来了一线希望。