溶血
免疫球蛋白D
生物
抗体
单克隆抗体
分子生物学
补体系统
免疫球蛋白M
单克隆
免疫学
免疫球蛋白G
B细胞
作者
Michael S. Neuberger,Klaus Rajewsky
标识
DOI:10.1002/eji.1830111212
摘要
Abstract The ability of monoclonal mouse IgM, IgD and IgG anti‐(4‐hydroxy‐3‐nitrophenyl) acetyl (NP) antibodies to activate mouse complement was studied using a hemolytic assay. Efficient hemolysis was obtained with IgG 2a , IgG 2b and IgG 3 antibodies but no lysis was observed using a monoclonal IgD. Of several IgG 1 antibodies tested, three gave no detectable hemolysis, although weak but significant hemoloysis was obtained with two other IgG 1 . IgM was found to be powerfully hemolytic in that it was effective at lower concentrations than were IgG. However, using complement from mouse strains carrying the H‐2 k haplotype it was found that, under conditions of complement limitation and saturating antibody, a fixed amount of complement could lyse about 3 to 4 times as many IgG‐coated sheep red cells as IgM‐coated red cells. This discrimination between IgM and IgG as regards the efficiency of complement utilization is controlled by a gene in the S region of H‐2 and is not apparent with complement from mice carrying the b, d or s allele at that locus.
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