Fig. 1.
Fig. 1. Two experimentally tested models. / (A) A putative autoantigen recognized by CD4+T cells is derived from GPI-anchored proteins. GPI+ cells (left) process GPI-anchored proteins and present antigenic peptides on MHC class II molecules, whereas GPI− cells (right) do not present such antigenic peptides. (B) Some GPI-anchored protein is a ligand for some costimulatory molecules on CD4+ T cells. GPI+ cells (left) efficiently stimulate CD4+ T cells, whereas GPI− cells (right) do not.

Two experimentally tested models.

(A) A putative autoantigen recognized by CD4+T cells is derived from GPI-anchored proteins. GPI+ cells (left) process GPI-anchored proteins and present antigenic peptides on MHC class II molecules, whereas GPI cells (right) do not present such antigenic peptides. (B) Some GPI-anchored protein is a ligand for some costimulatory molecules on CD4+ T cells. GPI+ cells (left) efficiently stimulate CD4+ T cells, whereas GPI cells (right) do not.

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