Suppr超能文献

帕金森病的疫苗接种。

Vaccination for Parkinson's disease.

机构信息

AFFiRiS AG, Karl-Farkas Gasse 22, A-1030 Vienna, Austria.

出版信息

Parkinsonism Relat Disord. 2012 Jan;18 Suppl 1:S11-3. doi: 10.1016/S1353-8020(11)70006-2.

Abstract

Idiopathic Parkinson's disease (PD) is, like other neurodegenerative diseases such as Alzheimer's disease (AD) considered a proteinopathy. Thus, a disease that is driven by the accumulation and aggregation of misfolded proteins, in case of PD α-synuclein (aSyn) is incriminated. Accordingly, removal of aSyn is assumed of having the potential to modify the course of the disease. Both active and passive aSyn targeting immunotherapy were found to modify disease in mice overexpressing human aSyn and recapitulating various aspects of synucleopathies. Translating immunotherapy to humans needs to consider the issue of potential autoimmunity. PD vaccines developed by AFFiRiS integrate the safety concept as applied for the company's AD vaccine candidates. This includes the use of short antigens, precluding activation of aSyn-specific T cells and, thus, cellular autoimmunity. Moreover, the selection of AFFITOPES® for clinical development is based on the principle of exclusive aSyn reactivity of vaccine-induced Abs excluding crossreactivity to β-synuclein (bSyn), which is ensured by the AFFITOME® platform technology. PD01, the first in class aSyn vaccine developed by AFFiRiS is about to enter the clinical phase of development.

摘要

特发性帕金森病 (PD) 与阿尔茨海默病 (AD) 等其他神经退行性疾病一样,被认为是一种蛋白质病。因此,在 PD 中,被归咎于错误折叠蛋白的积累和聚集,即α-突触核蛋白 (aSyn)。相应地,去除 aSyn 被认为具有改变疾病进程的潜力。主动和被动的 aSyn 靶向免疫疗法已被发现可改变过度表达人 aSyn 并重现各种突触核蛋白病特征的小鼠的疾病。将免疫疗法转化为人类需要考虑潜在自身免疫的问题。AFFiRiS 开发的 PD 疫苗整合了公司 AD 疫苗候选物所应用的安全性概念。这包括使用短抗原,排除了 aSyn 特异性 T 细胞的激活,从而排除了细胞自身免疫。此外,AFFITOPES® 的选择用于临床开发是基于疫苗诱导的 Abs 对 aSyn 反应的排他性原则,排除了对β-突触核蛋白 (bSyn) 的交叉反应性,这是由 AFFITOME® 平台技术确保的。AFFiRiS 开发的首个 aSyn 疫苗 PD01 即将进入开发的临床阶段。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验