Lymphocytes are white blood cells involved in the specific immune response.
Lymphocytes have a single type of membrane receptor which is specific for one antigen.
Antigen binding leads to repeated lymphocyte division resulting in the formation of a clonal population of identical lymphocytes.
B lymphocytes produce antibodies against antigens, and this leads to the destruction of the pathogen.
Antibodies are Y-shaped proteins that have receptor binding sites specific to a particular antigen or pathogen. Antibodies become bound to antigens, inactivating the pathogen.
The resulting antigen-antibody complex can then be destroyed by phagocytosis.
B-lymphocytes can respond to antigens on substances which are harmless to the body. E.g. Pollen
This hypersensitive response is called an allergic reaction.
Apoptosis is programmed cell death.
T lymphocytes destroy infected body cells by recognising antigens of the pathogen on cell membrane and inducing apoptosis.
T lymphocytes attach onto infected cells and release proteins. These proteins diffuse into infected cells causing the production of self-destructive enzymes which cause cell death.
The remains of the cell are then removed by phagocytosis.
Failure of regulation of the immune system leads to T lymphocytes responding to self-antigens. This causes autoimmune diseases.
In autoimmunity, the T-lymphocytes attack the body’s own cells. This causes autoimmune diseases such as type 1 diabetes and leukaemia.
Some of the cloned B and T lymphocytes survive long-term as memory cells.
The development of memory cells provides immunity.
When a secondary exposure to the same antigen occurs, these memory cells rapidly give rise to a new clone of specific lymphocytes.
These destroy invading pathogens before an individual starts to show any symptoms.
During the secondary response, antibody production is greater and more rapid than during the primary response.
Human immunodeficiency virus attacks and destroys T lymphocytes. HIV causes depletion of T lymphocytes which leads to the development of acquired immune deficiency syndrome or AIDS.
Individuals with AIDS have a weakened immune system and so are more vulnerable to opportunistic infections, such as pneumonia and influenza.
Phagocytes engulf pathogens and display antigens and become antigen presenting cells. These activate T-lymphocytes.