Long-term treatment of multiple sclerosis with glatiramer acetate: Natural history of the subtypes of anti-glatiramer acetate antibodies and their correlation with clinical efficacy

被引:34
|
作者
Karussis, Dimitros [1 ]
Teitelbaum, Dvora [2 ]
Sicsic, Camille [1 ]
Brenner, Talma [1 ]
机构
[1] Hadassah Hebrew Univ, Med Ctr, Dept Neurol, IL-91120 Jerusalem, Israel
[2] Weizmann Inst Sci, Dept Chem Immunol, IL-76100 Rehovot, Israel
关键词
Multiple sclerosis; Glatiramer acetate antibodies; Neutralizing antibodies; Antibody isotypes; Glatiramer acetate long-term treatment; EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; MYELIN BASIC-PROTEIN; T-CELL LINES; COPOLYMER; SYNTHETIC COPOLYMER-1; DISEASE; THERAPY; IMMUNOGENICITY; COPAXONE(R); SUPPRESSION;
D O I
10.1016/j.jneuroim.2010.01.009
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
A retrospective phase IV study was designed to evaluate the anti-GA antibody subtypes, test their in vitro neutralizing activity and correlate these parameters with the clinical efficacy, in long-term GA treatment of MS patients. Serum samples from 153 MS patients, 126 treated with GA for 2 to 15 years (mean 6.6 years) and 27 treated for <2 years, were collected. Anti-myelin basic protein (MBP) and anti-GA antibodies were measured by specific ELISA. Neutralizing activity was determined by the capacity of the serum to inhibit the proliferation of GA-specific T-cells. Anti-GA antibodies were detected even after very long treatment periods, although at lower levels. Anti-MBP reactivity remained consistently negative. The IgG2 isotype of anti-GA antibodies and the multiple sclerosis severity scale (MSSS) was lower in the long-term treated patients P=0.0003 and 0.016 respectively. The neutralizing activity of anti-GA antibodies was insignificant. Our results indicate that the clinical efficacy of GA treatment could be associated with a decrease in anti-GA IgG2 isotype in long-term GA-treated patients. (C) 2010 Elsevier B.V. All rights reserved.
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页码:125 / 130
页数:6
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