Myasthenia Gravis (MG) is an autoimmune disease mediated by antibodies dire
cted against the acetylcholine receptor (AChR). Treatment by IVIg is effect
ive in acute forms of myasthenia gravis. In order to determine the in vivo
effects of the various fractions of human immunoglobulins, we used an exper
imental model of myasthenia gravis in SCID mice. To this end, thymic cells
from MG patients are transferred to these mice according to a well defined
protocol. When establishing of the model, we noticed the appearance of anti
-AChR antibodies and the loss of AChR expression at the muscle level. After
treatment with IVIgG or IVIgM, the mice displayed a lower anti-AChR antibo
dy titer compared to control mice (albumin treated) and the loss of the ACh
R number at the muscle was significantly reduced. These results obtained fr
om one MG patient indicate that the human immunoglobulin preparations induc
e significant effects on pathogenic parameters in the SCID mouse model. The
refore this model is interesting to approach the mechanisms of action of hu
man immunoglobulins and deserves further investigation.