Melzer Nico, Harder Anja, Gross Catharina C, Wölfer Johannes, Stummer Walter, Niederstadt Thomas, Meuth Sven G, Marziniak Martin, Grauer Oliver Martin, Wiendl Heinz
Departments of Neurology, Inflammatory Disorders of the Nervous System, and Neurooncology, University of Münster, Albert-Schweitzer-Campus 1, Münster, 48149 Germany.
Arch Neurol. 2012 Jun;69(6):773-7. doi: 10.1001/archneurol.2011.2441.
In amyloid (Aβ)-related angiitis (ABRA)of the central nervous system (CNS), cerebral amyloid angiopathy occurs in association with primary vasculitis of small- and medium-sized leptomeningeal and cortical arteries. It has been suggested that ABRA is triggered by vascular deposition of A followed by an Aβ-directed (auto)immune response.
To provide a detailed description of the cellular composition of the inflammatory infiltrates in the cerebrospinal fluid (CSF) and CNS and their response to immunotherapy in a typical case of ABRA.
Report of a single case.
Neurologic referral center.
67-year-old white woman.
Neurologic examination,magnetic resonance imaging, lumbar puncture, flow cytometry,leptomeningeal biopsy, and histopathologic analysis.
In a typical case of ABRA, we demonstrate for the first time the presence of a vast majority of partially activated CD4(+) T cells in CSF and leptomeningeal and parenchymal (peri)vascular infiltrates, which were frequently found in close proximity to major histocompatibility complex (MHC) class II-expressing microglia, epithelioid macrophages, and multinucleated giant cells containing intracellular deposits of Aβ.
Our findings support the notion of adaptive Aß-directed autoimmunity as the underlying pathogenic mechanism in ABRA.
在中枢神经系统(CNS)的淀粉样蛋白(Aβ)相关血管炎(ABRA)中,脑淀粉样血管病与中小脑软膜和皮质动脉的原发性血管炎相关。有人提出,ABRA是由Aβ的血管沉积引发,随后是针对Aβ的(自身)免疫反应。
在一例典型的ABRA病例中,详细描述脑脊液(CSF)和中枢神经系统中炎性浸润的细胞组成及其对免疫治疗的反应。
单病例报告。
神经科转诊中心。
67岁白人女性。
神经学检查、磁共振成像、腰椎穿刺、流式细胞术、软脑膜活检和组织病理学分析。
在一例典型的ABRA病例中,我们首次证明在脑脊液以及软脑膜和实质(周围)血管浸润中存在绝大多数部分活化的CD4(+) T细胞,这些细胞经常在表达主要组织相容性复合体(MHC)II类分子的小胶质细胞、上皮样巨噬细胞和含有细胞内Aβ沉积物的多核巨细胞附近发现。
我们的研究结果支持适应性Aβ导向自身免疫是ABRA潜在致病机制的观点。