Abstract
Inducible costimulator (ICOS) is a new member of the CD28/CTLA-4 family that is expressed on activated and germinal center (GC) T cells. Recently, we reported that ICOS-deficient mice exhibited profound defects in T cell activation and effector function. Ab responses in a T-dependent primary reaction and in a murine asthma model were also diminished. In the current study, we investigate the mechanism by which ICOS regulates humoral immunity and examine B cell GC reactions in the absence of ICOS. We found that ICOS(-/-) mice, when immunized with SRBC, had smaller GCs. Furthermore, IgG1 class switching in the GCs was impaired. Remarkably, GC formation in response to a secondary recall challenge was completely absent in ICOS knockout mice. These data establish a critical role of ICOS in regulation of humoral immunity.
Publication types
-
Research Support, Non-U.S. Gov't
-
Research Support, U.S. Gov't, P.H.S.
MeSH terms
-
Animals
-
Antigens / administration & dosage
-
Antigens / immunology
-
Antigens, Differentiation, T-Lymphocyte / biosynthesis
-
Antigens, Differentiation, T-Lymphocyte / genetics
-
Antigens, Differentiation, T-Lymphocyte / immunology
-
Antigens, Differentiation, T-Lymphocyte / physiology*
-
B-Lymphocytes / immunology
-
B-Lymphocytes / metabolism
-
B-Lymphocytes / pathology
-
CD40 Ligand / biosynthesis
-
Germinal Center / immunology*
-
Germinal Center / metabolism*
-
Germinal Center / pathology
-
Immunization, Secondary
-
Immunoglobulin Class Switching / genetics
-
Immunoglobulin G / biosynthesis
-
Inducible T-Cell Co-Stimulator Protein
-
Lymphocyte Activation / genetics
-
Mice
-
Mice, Knockout
-
Peanut Agglutinin / biosynthesis
-
Sheep
-
Spleen / immunology
-
Spleen / metabolism
-
Spleen / pathology
-
T-Lymphocytes / immunology
-
T-Lymphocytes / metabolism
Substances
-
Antigens
-
Antigens, Differentiation, T-Lymphocyte
-
Icos protein, mouse
-
Immunoglobulin G
-
Inducible T-Cell Co-Stimulator Protein
-
Peanut Agglutinin
-
CD40 Ligand