期刊
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY
卷 49, 期 1, 页码 -出版社
WILEY
DOI: 10.1111/nan.12860
关键词
anti-alpha-Syn autoantibodies; immunotherapy; Parkinson's disease
P21 and P22 show promising potential for the treatment of Parkinson's disease by attenuating alpha-synuclein pathology and blocking its propagation.
Aims: Accumulation and propagation of pathological alpha-synuclein (alpha-Syn) are the major contributing factors to the pathogenesis of Parkinson's disease (PD). Therapy to halt the spreading of alpha-Syn pathology needs to be established. Methods: After phage display and affinity maturation, human-derived anti-alpha-Syn autoantibodies were selected and applied to biochemical, cellular and animal models of PD. Results: The novel naturally occurring anti-alpha-Syn autoantibodies (alpha-Syn-nAbs), P21 and P22, selectively bind alpha-Syn preformed fibrils (PFFs), recognise Lewy bodies (LBs) and Lewy neurites (LNs) in human PD brains, block a-Syn fibrillization and inhibit the seeding of alpha-Syn PFFs. Moreover, systematic administration of P21 and P22 attenuates alpha-Syn pathology, degeneration of the nigrostriatal pathway and motor deficits in mice injected with alpha-Syn PFFs. Conclusions: P21 and P22 attenuate alpha-synuclein pathology and are promising candidates for PD treatment.
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