Literature DB >> 35922733

Anti-Caspr-conjugated gold nanoparticles emergence as a novel approach in the treatment of EAE animal model.

Shirin Taghizadeh1, Morteza Motallebnezhad1, Tayebe Aghaie1, Maryam Azimi2, Azin Aghamajidi1, Ali-Akbar Salari3, Mahmoud Bozorgmehr4, Mohammad Ali Assarezadegan1,2, Mir Hadi Jazayeri5,6.   

Abstract

Multiple sclerosis (MS) is a chronic autoimmune disorder of central nervous system which is increasing worldwide. Although immunosuppressive agents are used for the treatment of MS disease, nevertheless the lack of non-toxic and efficient therapeutic method is perceptible. Hence, this study aims to evaluate the effect of Contactin-associated protein (Caspr) antibody-, poly ethylene glycol (PEG)- and exosome combined gold nanoparticles (GNPs) in comparison to Glatiramer acetate as a selective treatment of MS disease in the experimental autoimmune encephalomyelitis (EAE) mouse model. EAE was induced in female C57BL/6 mice and 25-day treatment with anti-Caspr-, PEG- and exosome combined GNPs was evaluated. Histopathological examination of spinal cord, regulatory T cells as well as inflammatory pathway including IFN-ɣ and IL-17 and mir-326 were investigated. The results showed the severity of MS symptoms was significantly decreased in all treated groups. Histological examination of the spinal cord indicated the reduced demyelination and immune cell infiltration. Besides, regulatory T cells were significantly increased following all treatments. Remarkably, the cytokine levels of IFN-ɣ and IL-17 as well as mir-326 is altered in treated groups. Taken together, the obtained findings demonstrate that the administration of anti-Caspr-, PEG- and exosome combined GNPs can be considered a potential treatment in MS disease.
© 2022. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

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Keywords:  Contactin-associated protein; Exosome; Experimental autoimmune encephalomyelitis; Gold nanoparticle; Multiple sclerosis; Poly ethylene glycol

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Year:  2022        PMID: 35922733     DOI: 10.1007/s11011-022-00981-y

Source DB:  PubMed          Journal:  Metab Brain Dis        ISSN: 0885-7490            Impact factor:   3.655


  1 in total

1.  Altered Expression of miR-326 in T Cell-derived Exosomes of Patients with Relapsing-remitting Multiple Sclerosis.

Authors:  Maryam Azimi; Mojdeh Ghabaee; Abdolreza Naser Moghadasi; Maryam Izad
Journal:  Iran J Allergy Asthma Immunol       Date:  2019-02       Impact factor: 1.464

  1 in total

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