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. 2021 Apr 19;28(1):29–48. doi: 10.1177/13524585211008760

Table 6.

Reported neuroprotective and regenerative effects of cellular biologics in animal models of MS.

Outcome Embryonic stem cells
Mesenchymal stem cells
Neural and glial precursor cells
Cuprizone Chemical demyelination EAE Chemical demyelination EAE/Viral
Increased viability of OPC and/or OLG ✓ ✓✓
Preserved quantity, function, or integrity of neurons/axons ✓ ✓ ✓ ✓ ✓ ✓✓✓
Protected against myelin loss and/or atrophy and lesions ✓ ✓ ✓ ✓ ✓✓ ✓ ✓✓ ✓✓✓✓✓✓✓
Reduced CNS oxidative stress, apoptosis, or cellular dysfunction ✓ ✓ ✓ ✓
Stimulated production of neurotrophins and growth factors ✓ ✓ ✓✓✓
Suppressed inflammatory microglial and/or astrocyte activation ✓ ✓ ✓ ✓ ✓ ✓ ✓✓
Promoted NPC/OPC proliferation or differentiation ✓ ✓ ✓ ✓ ✓ ✓ ✓ ✓✓✓ ✓✓✓✓✓✓✓✓✓
Induced migration and recruitment of NPC/OPC ✓ ✓ ✓✓ ✓✓✓
Induced formation of new myelin ✓ ✓ ✓ ✓ ✓ ✓ ✓✓ ✓✓✓✓
Suppressed myelin inhibitory factors
Improved neurological function (physical or cognitive) ✓ ✓ ✓ ✓ ✓ ✓ ✓ ✓✓✓✓✓✓✓

EAE: experimental autoimmune encephalomyelitis; NPC: neural precursor cell; OLG: oligodendrocyte; OPC: oligodendrocyte precursor cell.

Each check (✓) represents an observed outcome from an individual study.