Experimental MS Therapy Seen to Promote Myelin Regeneration in Preclinical Study

Margarida Azevedo, MSc avatar

by Margarida Azevedo, MSc |

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MS preclinical study

RegeneRx Biopharmaceuticals, Inc.,Ā announced the publication of a research article detailing the process by whichĀ Thymosin beta 4 (TĪ²4), the company’s novel therapeutic peptide, effectively promoted the remyelination process in two separate animal models commonly used for multiple sclerosis (MS) research. The article, ā€œThymosin beta4 promotes oligodendrogenesis in the demyelinating central nervous system,ā€ was published in the journal Neurobiology of Disease.

Myelin is a lipidic material that protects the nerve fibers in the central and peripheral nervous systems. Myelination, the process of myelin formation around neurons, is carried out by oligodendrocytes in the central nervous system (CNS). These mature cells do not have the capacity to replicate, so once they are destroyed the only way to reinitiateĀ myelination would be to recruit or generate oligodendrocyte progenitor cells (OPCs). These precursor cells may then proliferate and differentiate into myelin-producing mature oligodendrocytes.

Demyelination (the process of myelin destruction) is a hallmark of MS, leading to progressive neurodegeneration and synaptic failure. Currently no effective remyelination therapies are in use.

Researchers fromĀ the Departments of Neurology and Biostatistics and Research Epidemiology, Henry Ford Health System inĀ Detroit, and from the Department of Physics atĀ Oakland UniversityĀ inĀ Rochester, both in Michigan, showedĀ that TĪ²4 is an effective remyelination therapy, able to promote proliferation and differentiation of OPCs into mature,Ā myelin-producing oligodendrocytes, while also decreasing axonal damage. The research team also observed that the epidermal growth factor receptor (EGFR) signaling pathway contributes to this process.

Two different animal models extensively used in MS research, the experimental autoimmune encephalomyelitis (EAE) model and the cuprizone diet model, were used to evaluate this potential mechanism of CNS repair. In both, the improved rate of remyelination and mature oligodendrocytes generation significantly correlated with functional improvement in the mice.

The researchers concluded, ā€œthese findings indicated that: 1) TĪ²4 increases proliferation of OPCs and the maturation of OPCs to myelinating oligodendrocytes which in concert, likely contribute to the beneficial effect of TĪ²4, 2) Epidermal Growth Factor Receptor upregulated and activated by TĪ²4 may mediate the process of OPC differentiation, and 3) TĪ²4 could potentially be developed as a therapy for MS patients, and for other demyelinating neurological disorders,” according to a press release.

RegeneRx Biopharmaceuticals, based in Rockville, Maryland, isĀ clinical-stage drug development company focused on tissue protection, repair, and regeneration.