Standard Operating Procedure for the Good Manufacturing Practice-Compliant Production of Human Endometrial Stem Cells for Multiple Sclerosis.
Somayeh Ebrahimi-BaroughJafar AiMoloud PayabSepideh Alavi-MoghadamAmeneh ShokatiHamid Reza AghayanBagher LarijaniBabak ArjmandPublished in: Methods in molecular biology (Clifton, N.J.) (2021)
Multiple sclerosis (MS) is the most common cause of neurological diseases. Although, there are some effective medications with regulatory approval for treating MS, they are only partially effective and cannot promote repairing of tissue damage directly which occurs in the central nervous system. Therefore, there is an essential need to develop novel therapeutic approaches for neuroprotection or repairing damaged tissue in MS. Accordingly, cell-based therapies as a novel therapeutic strategy have opened a new horizon in treatment of MS. Each setting in cell therapy has potential benefits. Human endometrial stem cells as an invaluable source for cell therapy have introduced treatment for MS. In this respect, good manufacturing practice (GMP) has a pivotal role in clinical production of stem cells. This chapter tries to describe the protocol of GMP-grade endometrial stem cells for treatment of MS.
Keyphrases
- cell therapy
- multiple sclerosis
- stem cells
- mass spectrometry
- ms ms
- endothelial cells
- mesenchymal stem cells
- white matter
- healthcare
- randomized controlled trial
- primary care
- transcription factor
- risk assessment
- staphylococcus aureus
- combination therapy
- pseudomonas aeruginosa
- minimally invasive
- climate change
- cerebral ischemia
- cystic fibrosis
- induced pluripotent stem cells