Patients with myasthenia gravis have antibodies and T cells that react with
the beta 1- and beta 2-adrenergic receptors. These receptors, as well as o
ther auto-antigens, are present on cardiomyocytes, skeletal muscle cells an
d lymphocytes and are of importance for the regulation of the functions of
these organs. Antibodies against the beta 1-adrenergic receptor have been i
mplicated in dilated cardiomyopathies. Myasthenia gravis (MG) patients have
been suggested to have a higher than normal prevalence of heart disease. W
e have analysed the isotypes, subclasses, and binding sites of the beta-adr
energic receptors antibodies in both MG patients and healthy individuals an
d the correlation between beta-adrenergic receptors antibodies and heart di
sease in MG patients. The patients have IgG antibodies that react with both
beta 1- and beta 2-adrenergic receptors. The subclasses were predominantly
IgG2 and IgG4. By using synthesised overlapping peptides representing the
immunodominant regions an the receptors, it was shown that the antibodies b
ound to partially overlapping sites on both beta 1- and beta 2-adrenergic r
eceptors, but not to peptides from the acetylcholine receptor. beta-adrener
gic receptor antibodies were found in 34/125 MG patients. Seven out of thes
e 34 patients had symptomatic heart disease, all seven were over 70 years o
f age and had arteriosclerotic heart disease. There was no difference in th
e prevalence of clinical heart disease in patients with and without beta-ad
renergic receptor antibodies. However, patients with heart disease had sign
ificantly higher levels of antibodies than healthy individuals and other pa
tients. Antibodies against beta-adrenergic receptors in patients with myast
henia gravis binds to both beta 1- and beta 2-adrenergic receptors and migh
t be implicated in the few patients with myasthenia gravis who have heart d
isease. (C) 1998 Elsevier Science B.V. All rights reserved.