Immune response of SLE patients to peptides based on the complementarity determining regions of a pathogenic anti-DNA monoclonal antibody

被引:25
作者
Dayan, M
Segal, R
Sthoeger, Z
Waisman, A
Brosh, N
Elkayam, O
Eilat, E
Fridkin, M
Mozes, E [1 ]
机构
[1] Weizmann Inst Sci, Dept Immunol, IL-76100 Rehovot, Israel
[2] Ichilov Hosp, Dept Rheumatol, IL-64239 Tel Aviv, Israel
[3] Kaplan Hosp, Dept Internal Med B, IL-76100 Rehovot, Israel
[4] Weizmann Inst Sci, Dept Organ Chem, IL-76100 Rehovot, Israel
关键词
SLE; CDR-based peptides; T-cell proliferation; antigen presentation;
D O I
10.1023/A:1006685413157
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We have examined the humoral and cellular responses of SLE patients to peptides based on the complementarity-determining regions (CDR) of a monoclonal anti-DNA antibody with a major idiotype-16/6 Id, in comparison to their responses to the whole 16/6 Id-bearing antibody. Sera of 63% of the SLE patients had antibodies that bound the 16/6 Id, 80% had antibodies to one of the CDR-based peptides, and 40% of the patients reacted with both CDRs. Sera of only a few controls reacted with either the 16/6 Id (6%) or the CDR based peptides (48) (P < 0.01). Peripheral blood lymphocytes (PBL) of 39% of the patients proliferated in response to the 16/6 Id or to one of the CDR-based peptides (37%), while in the control group the proliferation rates were 66% to the 16/6 Id and 59% to one of the CDR-based peptides (P < 0.05). The correlation between (both) the humoral and cellular immune responses to the CDR-based peptides and to the 16/6 Id suggests the relevance of these peptides to the 16/6 Id and provides additional information on the pathogenic moiety of the latter antibody.
引用
收藏
页码:187 / 194
页数:8
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