Humoral and cellular immune responses to Copolymer 1 in multiple sclerosis patients treated with Copaxone®

被引:104
作者
Brenner, T
Arnon, R
Sela, M
Abramsky, O
Meiner, Z
Riven-Kreitman, R
Tarcik, N
Teitelbaum, D [1 ]
机构
[1] Weizmann Inst Sci, Dept Immunol, IL-76100 Rehovot, Israel
[2] Hadassah Univ Hosp, Dept Neurol, IL-91120 Jerusalem, Israel
[3] Teva Pharmaceut, R&D Div, Netanya, Israel
关键词
glatiramer acetate; Copolymer; 1; anti-Cop1; antibodies; T cell proliferation; IgG1/IgG2; Th1/Th2;
D O I
10.1016/S0165-5728(01)00250-8
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Humoral and cellular immune responses were followed in multiple sclerosis patients treated with Copolymer 1 (Cop1, glatiramer acetate, Copaxone(R)) who participated in three different clinical trials. All patients (130) developed Cop1 reactive antibodies, which peaked at 3 months after initiation of treatment, decreasing at 6 months and remaining low. IgG1 antibody levels were 2-3-fold higher than those of IgG2. The proliferative response of Peripheral Blood Mononuclear Cells (PBMC) to Cop1 was initially high and gradually decreased during treatment. Antibodies and T cell responses to MBP were low and did not change significantly during the treatment. The humoral and cellular immunological responses to Cop1 do not correlate with the side effects and do not affect its therapeutic activity. The preferential production of IgG1 over IgG2 antibodies may indicate that Th2 responses are involved in mediating the clinical effect of Cop1. (C) 2001 Published by Elsevier Science B.V.
引用
收藏
页码:152 / 160
页数:9
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