| Literature DB >> 29150266 |
Samira Moghadam1, Maryam Erfanmanesh2, Abdolreza Esmaeilzadeh3.
Abstract
An autoimmune demyelination disease of the Central Nervous System, Multiple Sclerosis, is a chronic inflammation which mostly involves young adults. Suffering people face functional loss with a severe pain. Most current MS treatments are focused on the immune response suppression. Approved drugs suppress the inflammatory process, but factually, there is no definite cure for Multiple Sclerosis. Recently developed knowledge has demonstrated that gene and cell therapy as a hopeful approach in tissue regeneration. The authors propose a novel combined immune gene therapy for Multiple Sclerosis treatment using anti-inflammatory and remyelination of Interleukine-35 and Hepatocyte Growth Factor properties, respectively. In this hypothesis Interleukine-35 and Hepatocyte Growth Factor introduce to Mesenchymal Stem Cells of EAE mouse model via an adenovirus based vector. It is expected that Interleukine-35 and Hepatocyte Growth Factor genes expressed from MSCs could effectively perform in immunotherapy of Multiple Sclerosis.Entities:
Keywords: CNS; Hepatocyte Growth Factor; Interleukine-35; Mesenchymal Stem Cells; Multiple Sclerosis
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Year: 2017 PMID: 29150266 DOI: 10.1016/j.mehy.2017.09.017
Source DB: PubMed Journal: Med Hypotheses ISSN: 0306-9877 Impact factor: 1.538