生发中心
免疫球蛋白D
CD40
23号公路
免疫球蛋白类转换
生物
免疫系统
B细胞
免疫球蛋白M
免疫学
免疫球蛋白E
抗原
抗体
幼稚B细胞
亲和力成熟
分子生物学
免疫球蛋白G
B-1电池
记忆B细胞
CD154
T细胞
细胞生物学
B细胞受体
抗原提呈细胞
体外
细胞毒性T细胞
遗传学
作者
Tsutomu Kawabe,Tetsuji Naka,Kyotaro Yoshida,Takashi Tanaka,Hiroshi Fujiwara,Sachiko Suematsu,Nobuaki Yoshida,Tadamitsu Kishimoto,Hitoshi Kikutani
出处
期刊:Immunity
[Elsevier]
日期:1994-06-01
卷期号:1 (3): 167-178
被引量:1055
标识
DOI:10.1016/1074-7613(94)90095-7
摘要
An engagement of CD40 with CD40 ligand (CD40L) expressed on activated T cells is known to provide an essential costimulatory signal to B cells in vitro. To investigate the role of CD40 in in vivo immune responses, CD40-deficient mice were generated by gene targeting. The significant reduction of CD23 expression on mature B cells and relatively decreased number of IgM bright and IgD dull B cells were observed in the mutant mice. The mutant mice mounted IgM responses but no IgG, IgA, and IgE responses to thymusdependent (TD) antigens. However, IgG as well as IgM responses to thymus-independent (TI) antigens were normal. Furthermore, the germinal center formation was defective in the mutant mice. These results suggest that CD40 is essential for T cell-dependent immunoglobulin class switching and germinal center formation, but not for in vivo T cell-dependent IgM responses and T cell-independent antibody responses.
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