Myasthenia gravis (MG) is undoubtedly the most thoroughly understood o
f all human autoimmune diseases. The basic defect in the disease is a
decrease in the number of available acetylcholine receptors (AChR) at
neuromuscular junctions caused by an antibody-mediated autoimmune atta
ck. Current treatments aimed at restoring the available AChR, depletin
g the autoantibodies or suppressing the immune system have been so eff
ective that most patients can lead normal lives. However, prolonged dr
ug treatment is required, and this carries a potential risk of drug to
xicity and, in the case of immunosuppressants, systemic immunosuppress
ion. The ideal treatment for MG would eliminate only the abnormal auto
immune response without interfering with the immune system. During the
past 20 years, impressive advances have been made in our understandin
g of the immunology and molecular biology of MG. Accordingly, it shoul
d be possible to design rational and immune-based therapies in the fut
ure. in this article, we briefly review the current treatment modaliti
es for MG, and discuss the prospects for immunotherapy.