USE OF ANTIPEPTIDE ANTIBODIES FOR THE DESIGN OF ANTIGEN-SPECIFIC IMMUNE-COMPLEX ASSAYS

被引:16
作者
MARUYAMA, T
THORNTON, GB
IINO, S
KUROKAWA, K
MILICH, DR
机构
[1] SCRIPPS RES INST, DEPT MOLEC BIOL, LA JOLLA, CA 92037 USA
[2] RW JOHNSON PHARMACEUT RES INST, SAN DIEGO, CA 92121 USA
[3] UNIV TOKYO, FAC MED, DEPT INTERNAL MED 1, TOKYO 113, JAPAN
关键词
HEPATITIS-B VIRUS; CHRONIC INFECTION; HEPATITIS-B SURFACE ANTIGEN; HEPATITIS-B E ANTIGEN;
D O I
10.1016/0022-1759(92)90272-U
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A simple and sensitive method is described for the detection of circulating immune complexes (ICs) in an antigen-specific manner. The method is based on the use of anti-peptide antibodies as solid-phase capture reagents to bind antigen which is complexed to serum antibodies. The bound serum antibody is detected with a labelled second antibody. The method requires that the anti-peptide antibodies bind native protein efficiently, and that the anti-peptide antibodies do not compete with antibodies raised against the native protein which are involved in IC formation. Two anti-peptide antibodies specific for the hepatitis B surface antigen (HBsAg) and the hepatitis B e antigen (HBeAg), which possessed the requisite characteristics, were chosen as models for IC assay development. The solid-phase, anti-peptide based assays efficiently detected HBsAg and HBeAg-containing ICs in preformed antigen/antibody mixtures and in the serum of chronically infected hepatitis B patients.
引用
收藏
页码:65 / 75
页数:11
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