Development of monkey C-reactive protein (CRP) assay methods

被引:13
作者
Jinbo, T
Hayashi, S
Iguchi, K
Shimizu, M
Matsumoto, T
Naiki, M
Yamamoto, S [1 ]
机构
[1] Azabu Univ, Fac Environm & Hlth Sci, Dept Immunol, Sagamihara, Kanagawa 229, Japan
[2] Natl Inst Hlth, Dept Vet Sci, Shinjuku Ku, Tokyo 162, Japan
关键词
C-reactive protein; monkey; enzyme-linked immunosorbent assay; turbidimetric immunoassay;
D O I
10.1016/S0165-2427(97)00148-7
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Monkey-specific C-reactive protein (CRP) assay methods (enzyme-linked immunosorbent assay (ELISA) and turbidimetric immunoassay (TIA)) were developed. The anti-monkey CRP serum was prepared by immunization of rabbits with the immune complex formed between the acute-phase serum from turpentine oil-inoculated monkeys and goat anti-human CRP serum. The specificity of the rabbit anti-monkey CRP serum was confirmed by immunoelectrophoresis and Western blotting. The purity of monkey CRP prepared by chromatography procedures was confirmed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE). The serum CRP levels in nine normal monkeys, as measured by sandwich ELISA were ranged from 0.26 to 1.42 mu g/ml (mean 0.71 +/- 0.37). The CRP levels in five acute-phase sera of turpentine oil-inoculated monkeys were 248-451 mu g/ml (mean 371.2 +/- 73.8). This monkey-specific CRP assay method was found more sensitive than the human-specific CRP assay method in detecting monkey CRP by TIA. (C) 1998 Elsevier Science B.V.
引用
收藏
页码:195 / 202
页数:8
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