Multiple sclerosis (MS) is a chronic neurological disease that
affects the brain and spinal cord. It is thought that MS is an
autoimmune disease, where a person’s immune system reacts to
its own body, namely the myelin sheath that surrounds the nerve
cells. Disease symptoms include vision problems, imbalance and
paralysis of the limbs. The exact cause of MS is still unknown, and
therapies without adverse effects are not available. Substantial
evidence suggests that the disease arises as a result of a certain
combination of environmental, genetic and infectious
circumstances. We hypothesize that herpesviruses create a
repertoire of autoreactive T-cells, which play a crucial role in the
demyelination process. To unravel the contribution of these
autoreactive T-cells to the pathogenesis of MS, the common
marmoset is used as an animal model for MS. The common
marmoset is a relevant model with a close genetic and
immunological proximity to humans, and it resembles the
disease in its clinical and pathological presentation. This thesis
describes how the common marmoset model for MS is refined
ethically, mechanistically, and conceptually to better understand
the underlying pathogenic processes, as well as to develop and
improve new targets for MS therapy.
http://repub.eur.nl/res/pub/32462/120523_Jagessar%2C%20Sunil%20Anwar_Bewerkt.pdf
http://repub.eur.nl/res/pub/32462/120523_Jagessar%2C%20Sunil%20Anwar_Bewerkt.pdf