AUTOIMMUNE REACTIONS IN PATIENTS WITH M-COMPONENT AND PERIPHERAL NEUROPATHY

被引:6
作者
JONSSON, V
SCHRODER, HD
TROJABORG, W
JENSEN, TS
HIPPE, E
HANSEN, MM
机构
[1] UNIV COPENHAGEN, RIGSHOSP, DEPT NEUROPHYSIOL, DK-2100 COPENHAGEN, DENMARK
[2] UNIV COPENHAGEN, GENTOFTE HOSP, DEPT HAEMATOL, DK-1168 COPENHAGEN, DENMARK
[3] AARHUS UNIV, AARHUS MUNICIPAL HOSP, DEPT NEUROL, DK-8000 AARHUS, DENMARK
关键词
AUTOIMMUNITY; MAG ANTIBODIES; M-COMPONENT; MONOCLONAL GAMMOPATHY; PERIPHERAL NEUROPATHY; PLASMA CELL DYSCRASIA;
D O I
10.1111/j.1365-2796.1992.tb00570.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
A study of 17 patients with autoimmune axonal or demyelinating peripheral neuropathy in combination with M-component is described. The M-component was associated with MGUS (monoclonal gammopathy of undetermined significance) in 12 patients, CLL in one patient, Waldenstrom's disease in one patient, and myeloma in three patients Immunohistological examination with direct and indirect fluorescence showed binding of antibodies to nerve structures of the same class and light chain as seen in the M-component. In five cases of IgM M-component, the demyelinating neuropathy was caused by binding of the IgM M-protein and complement C3b to myelin-associated glycoproteins (MAG). In 12 cases with axonal neuropathy, binding of IgG to the connective tissue of the peri- and endoneurium was found in 50% of cases, IgM in five cases, and IgD in one case. None of the patients had central nervous system (CNS) symptoms. The clinical and therapeutic difficulties are discussed; only two patients with an acute course responded to immunosuppression. A marked co-expression of other autoimmune phenomena is interpreted in the light of cross-reactions between the autoantibody and similar tissue autoantigens.
引用
收藏
页码:185 / 191
页数:7
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