The process where the one type of lymphocyte already present that has the complementary proteins to those of the pathogen is stimulated to divide to build up its numbers to a level where it can be effective in destroying it
In the foetus, lymphocytes are constantly colliding with other cells, but infection is rare because it is protected from the outside world by the mother and the placenta
Lymphocytes that show an immune response to self-antigens undergo programmed cell death before they can differentiate into mature lymphocytes, leaving only those that might respond to non-self-antigens
The response is immediate in non-specific but slower in specific. The non-specific is the same for all pathogens but the specific is specific to each pathogen
Usually proteins that are part of the cell surface membranes or cell walls of invading cells, such as microorganisms, or abnormal body cells, such as cancer cells
The presence of an antigen triggers the production of an antibody as part of the body's defence system
1. Lymphocytes respond to an organism's old cells that have been infected by non-self-material from a different species
2. Lymphocytes respond to cells from other individuals of the same species because these are genetically different and have different antigens on their cell surface membrane
3. Phagocytes that have engulfed and hydrolysed a pathogen present some of the pathogen's antigens on their own surface membrane
4. Body cells invaded by a virus present some of the viral antigens on their own cell-surface membrane
5. Transplanted cells from individuals of the same species have different antigens on their cell-surface membrane
6. Cancer cells are different from normal body cells and present antigens on their cell-surface membranes
Response of T lymphocytes to infection by a pathogen
1. Pathogens invade body cells or are taken in by phagocytes
2. The phagocyte places antigens from the pathogen on its cell-surface membrane
3. Receptors on a specific helper T cell fit exactly onto these antigens
4. This attachment activates the T cell to divide rapidly by mitosis and form a clone of genetically identical cells
5. The cloned T cells develop into memory cells that enable a rapid response to future infections by the same pathogen, stimulate phagocytes to engulf pathogens by phagocytosis, stimulate B cells to divide and secrete their antibody, and activate cytotoxic T cells