REMOVAL OF ANTIACETYLCHOLINE RECEPTOR ANTIBODIES BY PROTEIN-A IMMUNOADSORPTION IN MYASTHENIA-GRAVIS

被引:33
|
作者
BERTA, E
CONFALONIERI, P
SIMONCINI, O
BERNARDI, G
BUSNACH, G
MANTEGAZZA, R
CORNELIO, F
ANTOZZI, C
机构
[1] IST NAZL NEUROL C BESTA,NEUROMUSCULAR RES CTR,DIV MALATTIE NEUROMUSCOLARI,I-20133 MILAN,ITALY
[2] IST NAZL NEUROL C BESTA,DEPT LAB INVEST,I-20133 MILAN,ITALY
[3] OSPED NIGUARDA CA GRANDA,DEPT NEPHROL,MILAN,ITALY
关键词
PROTEIN A; IMMUNOADSORPTION; PLASMAPHERESIS; MYASTHENIA GRAVIS; ANTIACETYLCHOLINE RECEPTOR ANTIBODIES; IMMUNOGLOBULINS;
D O I
10.1177/039139889401701109
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Myasthenia Gravis is an autoimmune disease in which autoantibodies to the acetylcholine receptor interfere with neuromuscular transmission. Plasma exchange is effective in temporarily relieving the symptoms of the disease, but for repeated use the lack of selectivity and need for replacement fluids (which increases the risk of contracting viral diseases) are important drawbacks. Staphylococcal protein A, a potent ligand for immuno-globulins, that interacts negligibly with other plasma proteins, appears to be an optimal candidate for removing antiacetylcholine receptor antibodies, which are mostly IgG. We treated three patients with severe immunosuppression-resistant myasthenia gravis with protein A immunoadsorption. Neurological impairment significantly improved in all patients. After immunoadsorption of 1.5-2 plasma volumes per session, the mean percentage reductions for serum IgG and specific autoantibodies were 71% and 82% respectively. No major side effects occurred. Protein A immunoadsorption appears to be a safe, efficient and effective alternative to plasmaexchange for selected myasthenic patients requiring prolonged apheresis.
引用
收藏
页码:603 / 608
页数:6
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