Promising Nanotechnology Approaches in Treatment of Autoimmune Diseases of Central Nervous System

被引:37
作者
Chountoulesi, Maria [1 ]
Demetzos, Costas [1 ]
机构
[1] Natl & Kapodistrian Univ Athens, Sch Hlth Sci, Dept Pharm, Sect Pharmaceut Technol, Athens 15771, Greece
关键词
multiple sclerosis; nanotechnology; drug delivery nanosystems; lipids; polymers; vaccines; nanoparticles; antigen-specific immunotherapy; experimental autoimmune encephalomyelitis; neurodegeneration; NANOSTRUCTURED LIPID CARRIERS; ENHANCED BRAIN DELIVERY; MULTIPLE-SCLEROSIS; ANIMAL-MODELS; T-CELLS; POLYMERIC NANOPARTICLES; THERAPEUTIC-EFFICACY; DRUG; REMYELINATION; PEPTIDE;
D O I
10.3390/brainsci10060338
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Multiple sclerosis (MS) is a chronic, autoimmune, neurodegenerative disease of the central nervous system (CNS) that yields to neuronal axon damage, demyelization, and paralysis. Although several drugs were designed for the treatment of MS, with some of them being approved in the last few decades, the complete remission and the treatment of progressive forms still remain a matter of debate and a medical challenge. Nanotechnology provides a variety of promising therapeutic tools that can be applied for the treatment of MS, overcoming the barriers and the limitations of the already existing immunosuppressive and biological therapies. In the present review, we explore literature case studies on the development of drug delivery nanosystems for the targeted delivery of MS drugs in the pathological tissues of the CNS, providing high bioavailability and enhanced therapeutic efficiency, as well as nanosystems for the delivery of agents to facilitate efficient remyelination. Moreover, we present examples of tolerance-inducing nanocarriers, being used as promising vaccines for antigen-specific immunotherapy of MS. We emphasize on liposomes, as well as lipid- and polymer-based nanoparticles. Finally, we highlight the future perspectives given by the nanotechnology field toward the improvement of the current treatment of MS and its animal model, experimental autoimmune encephalomyelitis (EAE).
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页数:23
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