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Published on: January 14, 2011
Costimulatory molecules and T-cell-B-cell interactions
1Mary Kirkland Center, for Lupus Research, Hospital for Special Surgery, 535 East 70th Street, New York, NY 10021, USA. crowm@hss.edu
This article focuses on activating and inhibiting costimulatory signals that are delivered to the T cell from antigen-presenting cells, mediating and modulating T-cell clonal expansion and development of effector functions, as well as costimulatory signals that are delivered by activated T cells to interacting target cells. The coordinated expression and interaction of these molecules regulates responses to foreign antigens and avoidance of response to self-antigens. Knowledge of the structure and function of these costimulatory molecules can be used to manipulate immune function and inhibit autoimmunity and inflammation in the setting of disease.
This article focuses on activating and inhibiting costimulatory signals that are delivered to the T cell from antigen-presenting cells, mediating and modulating T-cell clonal expansion and development of effector functions, as well as costimulatory signals that are delivered by activated T cells to interacting target cells. The coordinated expression and interaction of these molecules regulates responses to foreign antigens and avoidance of response to self-antigens. Knowledge of the structure and function of these costimulatory molecules can be used to manipulate immune function and inhibit autoimmunity and inflammation in the setting of disease.
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