The immune responses in CD40-deficient mice: impaired immunoglobulin class switching and germinal center formation
T Kawabe, T Naka, K Yoshida, T Tanaka, H Fujiwara… - Immunity, 1994 - Elsevier
T Kawabe, T Naka, K Yoshida, T Tanaka, H Fujiwara, S Suematsu, N Yoshida, T Kishimoto…
Immunity, 1994•ElsevierAn 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) …
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) …
Abstract
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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