Kile Shawn J, Olichney John M
Department of Neurology, University of California, Davis.
Alzheimers Dis Res J. 2007;1(1-2):5-12.
Immunization strategies which aid in the clearance of beta-amyloid (Aβ) plaques have raised new hopes for the treatment of Alzheimer's disease (AD). Two particularly promising passive immunization therapies currently being investigated include intravenous immunoglobulins (IVIG) containing Aβ antibodies and specifically developed monoclonal antibodies for Aβ. These Aβ antibodies may reduce amyloid accumulation in the brain by binding to the amyloid peptide and drawing it in through the blood-brain barrier for subsequent removal from the capillaries. However, as this strategy aims at removing extracellular amyloid through cerebral vessels, a redistribution of amyloid pathology may manifest as increased cerebral amyloid angiopathy (CAA). CAA occurs when Aβ becomes embedded in the walls of cerebral vessels associated with weakening of the vessel walls. Antibody mediated Aβ clearance from the parenchyma could significantly increase the Aβ burden in the vessel lumen and wall, therefore increasing the risk of vessel rupture and hemorrhage. This chapter will review the current literature on Aβ immunotherapy for AD and explore the mechanisms as well as possible risks of amyloid clearance treatment, particularly cerebral amyloid angiopathy.
有助于清除β-淀粉样蛋白(Aβ)斑块的免疫策略为阿尔茨海默病(AD)的治疗带来了新希望。目前正在研究的两种特别有前景的被动免疫疗法包括含有Aβ抗体的静脉注射免疫球蛋白(IVIG)和专门开发的针对Aβ的单克隆抗体。这些Aβ抗体可能通过与淀粉样肽结合并将其通过血脑屏障吸入,从而减少大脑中的淀粉样蛋白积累,以便随后从毛细血管中清除。然而,由于该策略旨在通过脑血管清除细胞外淀粉样蛋白,淀粉样病理的重新分布可能表现为脑淀粉样血管病(CAA)增加。当Aβ嵌入与血管壁变薄相关的脑血管壁时,就会发生CAA。抗体介导的Aβ从实质中清除可能会显著增加血管腔和血管壁中的Aβ负担,从而增加血管破裂和出血的风险。本章将综述目前关于AD的Aβ免疫疗法的文献,并探讨淀粉样蛋白清除治疗的机制以及可能的风险,特别是脑淀粉样血管病。