- Recognises the antigens on the pathogen as non-self
- Phagocyte engulfs the pathogen
- Pathogen then contained in a type of vesicle called a phagosome
- A lysosome joins with the phagosome to make a phagolysosome
- Enzymes in the phagolysosome break down the pathogen, saving the antigens to present
-Phagocyte becomes an APC (antigen-presenting cell)
Formation of APC activates T lymphocytes which have receptors on their surfaces
- Receptors bind to the antigens until they find a shape that is complementary
- The T lymphocyte that has the complementary receptor is then chosen for mass production --> clonal selection
- The clonally selected T lymphocyte the undergoes clonal expansion where it divides by mitosis LOADS
Each new T lymphocyte differentiates into 1 of the 4 variants
T helper cells --> release substances (such as interleukins) to active B lymphocytes and T killer cells
T killer cells --> attach to and kill cells infected with virus
T regulatory cells --> suppress the immune system when the threat is almost gone to prevent it attacking host's healthy body cells
T memory cells --> remember the specific antigen and will recognise it again
B lymphocytes are covered with antibodies :
- Antibodies bind to antigens on the APC to find the one that's shape is complemtary
- When they match, the B lymphocyte is clonally selected
- The selected B lymphocyte then undergoes clonal expansion --> divides by mitosis into plasma cells and B memory cells
Plasma cells are clones of the B lymphocytes but can produce LOADS of antibodies
B memory cells --> remember the specific antibodies that join to specific antigens
Autoimmune diseases happen when these aren't right