Multiple sclerosis (MS),the most common neurological autoimmune disord
er diagnosed in young adults, is characterised by the repeated occurre
nce of demyelinating lesions within the central nervous system (CNS).
Promotion of remyelination in the brain and spinal cord constitutes a
potential strategy for therapeutic intervention in MS and other demyel
inating diseases. Three different principles are known to promote remy
elination in the CNS of different animal models: Application of growth
factors, transplantation of myelin-forming cells and intravenous immu
noglobulin (IVIg) therapy. However, the systemic application of growth
factors could be limited by effects on unaffected tissue. For success
ful transplantation we still have the problem of homologous cells not
tolerated by a immunological different organism. Currently the require
d combination of growth factors needed to cultivate human homologous c
ells is not known,so that cells suitable for transplantation are still
not available. Nevertheless, there is increasing evidence for benefic
ial effects of IVIg therapy on the promotion of remyelination in human
s. In this review we summarise recent findings on the regulation of my
elin sheath development and oligodendrocyte differentiation,and discus
s the presented strategies in the context of possible clinical applica
tion for the therapy of MS.