Department of Neurology of Memory and Language, GHU Paris Psychiatrie & Neurosciences, Hôpital Sainte-Anne, Paris, France.
Université Paris-Cité, Paris, France.
Nat Aging. 2024 Jun;4(6):761-770. doi: 10.1038/s43587-024-00630-2. Epub 2024 Jun 5.
The cautious optimism following recent anti-amyloid therapeutic trials for Alzheimer's disease (AD) provides a glimmer of hope after years of disappointment. Although these encouraging results represent discernible progress, they also highlight the need to enhance further the still modest clinical efficacy of current disease-modifying immunotherapies. Here, we highlight crucial milestones essential for advancing precision medicine in AD. These include reevaluating the choice of therapeutic targets by considering the key role of both central neuroinflammation and peripheral immunity in disease pathogenesis, refining patient stratification by further defining the inflammatory component within the forthcoming ATN(I) (amyloid, tau and neurodegeneration (and inflammation)) classification of AD biomarkers and defining more accurate clinical outcomes and prognostic biomarkers that better reflect disease heterogeneity. Next-generation immunotherapies will need to go beyond the current antibody-only approach by simultaneously targeting pathological proteins together with innate neuroinflammation and/or peripheral-central immune crosstalk. Such innovative immunomodulatory combination therapy approaches should be evaluated in appropriately redesigned clinical therapeutic trials, which must carefully integrate the neuroimmune component.
近年来,针对阿尔茨海默病(AD)的抗淀粉样蛋白治疗试验带来了谨慎的乐观,这为多年来的失望带来了一线希望。尽管这些令人鼓舞的结果代表了明显的进展,但它们也突出表明需要进一步提高当前疾病修饰性免疫疗法的仍然有限的临床疗效。在这里,我们强调了推进 AD 精准医学的关键里程碑。这些包括通过考虑中枢神经炎症和外周免疫在疾病发病机制中的关键作用,重新评估治疗靶点的选择,通过进一步定义即将到来的 AD 生物标志物的 ATN(I)(淀粉样蛋白、tau 和神经退行性变(和炎症)分类中的炎症成分,来细化患者分层,并定义更准确的临床结果和预后生物标志物,以更好地反映疾病异质性。下一代免疫疗法需要超越当前仅抗体的方法,同时针对病理蛋白以及固有神经炎症和/或外周-中枢免疫相互作用。此类创新的免疫调节联合治疗方法应在经过重新设计的临床治疗试验中进行评估,这些试验必须仔细整合神经免疫成分。