1. Antigen-presenting cells, such as macrophages, phagocytize, process, and display antigens on the cell’s surface.
2. The antigens are bound to MHC class II molecules, which present the processed antigen to the T-cell receptor of the helper T cell.
3. Costimulation results from interleukin-1, secreted by the macrophage, and the CD4 glycoprotein of the helper T cell.
4. Interleukin-1 stimulates the helper T cell to secrete interleukin-2 and to produce interleukin-2 receptors.
5. The helper T cell stimulates itself to divide when interleukin-2 binds to interleukin-2 receptors.
6. The “daughter” helper T cells resulting from this division can be stimulated to divide again if they are exposed to the same antigen that stimulated the “parent” helper T cell. This greatly increases the number of helper T cells.
7. The increased number of helper T cells can facilitate the activation of B cells or effector T cells.