specific immune system - can target a specificpathogen, although it is slower to act
specific immune system
cellular response
humoral response
antigens:
unique molecules (glycoproteins and glycolipids) found on the surface of cells
antigens allow the immune system to distinguish between the body's cells (self) and foreign cells (non-self).
antibodies
y-shapedglycoproteins made up of 4 polypeptide chains called immunoglobins
2 heavy chains and 2 light chains
antibody:
peptide chains are held together by disulphide bridges
constant region - same for all antibodies and bindto receptors on cells
variable region - different for each antibody as its shape is complementary to a specific antigen
hing region - this allows the antibody to be flexible so it can bind to multiple antigens at once
antibodies bind to antigens on a lock and key mechanisms, forming an antigen-antibody complex
Antibodies role of destroying pathogens:
agglutination
neutralisation of toxins
prevention of pathogens binding
agglutination of pathogens:
causes pathogens carrying antigen-antibody complex to clump together
makes it easier for phagocytes to locate pathogens and allows them to engulf a number of pathogens at once.
antibodies also act as opsonins, making pathogens easily recognisable by phagocytes.
Neutralisation of toxins:
antibodies act as anti-toxins where they bind to toxins produced by pathogens
this binding neutralises (inactivates) the toxin to prevent them damaging body cells
Preventing pathogens binding to cells:
when antibodies bind to pathogens antigens, they block cell surface receptors needed to bind to host cells
this means that the pathogen cannot bind to host cells
lymphocytes - a type of white blood cell, that are produced in the bone marrow
recognise antigen molecules on the surface of pathogens and co-ordinate an immune response against that pathogen
Blymphocytes/B cells - mature in the bone marrow. They are involved in the humoral response where they produce antibodies found in body fluids
Tlymphocytes/T cells - mature in the thymus gland. Involved in the cellular response where they respond to antigens present presented on body cells.
Types of T lymphocytes:
T helper cells
T killer cells
T memory cells
T regulator cells
Thelper cells:
These cells have receptors on their cell surface that bind to complementaryantigens on APC's.
They produce interleukins (a type of cytokine) which stimulate B cells or phagocytes.
T helper cells can also form memory cells or T killer cells.
T killer cells
These cells destroy the pathogen by producing a chemical called perforin.
Perforin makes holes in the cell surface membrane, causing it to become freely permeable and causing cell death.
Tmemory cells:
live for a long time and are part of the immunologicalmemory
if they meet an antigen a second time, they divide rapidly to form a hig number of clones of T-killer cells that destroy the pathogen.
T regulator cells:
These cells suppress the immune system after pathogens have been destroyed.
This helps to prevent the immune system from mistakenly attacking the body cells.
Types of B lymphocytes:
plasma cells
B effector cells
B memory cells
B lymphocytes:
These cells have antibodies on their cell-surface membrane that bind to complementary antigens.
On doing so, they engulf the antigens and display them on their cell-surface to become antigen-presenting cells.
Once activated, B cells can divide into plasma cells and memory cells.
Plasma cells:
produce antibodies to a specific antigen and release them into the circulation
short lifespan
B effector cells:
divide to form plasma cell clones
B memory cells:
remain in the blood for a long time, providing immunological memory
They rapidly divide if the body is re-infected by the same specific pathogen.
stages of cellular response/cell mediated:
Macrophagesengulfpathogens and display their antigens on the cell surface. They are now known as antigen-presenting cells (APC's)
T helper cells with complementaryreceptors bind to these antigens.
T helper cells become activated and produce interleukins (stimulating phagocytosis) and divide by mitosis to form genetically identical clones
cloned T cells develop into T memory cells, T killer cells and stimulate B cells to divide
humoral response:
response to pathogens found in the blood stream, mainly bacteria and fungal
anti-bodies are produced that are soluble in the blood, tissue and lymph fluid
B cells have anti-bodies on their surface and will bind to the complementary antigens on pathogens membrane
B cells will engulf the pathogen and present the antigen on its surface (APC)
Humoral response steps:
B cell engulfs pathogen, presents its antigens on the membrane becomes APC.
Activated T helper cells bind to B cell (APC), activation of this B cell - clonalselection
interleukins produced by activated T helper cells activate B cells
activated B cell divides to form plasma & memory cell clones - clonal expansion
cloned plasma cells produce & secrete specific antibody which is specific to antigen on pathogen's surface.
memory cells circulate blood, ready to divide if the body is re-infected by same pathogen.
clonal selection - The B cell with the correct antibody is selected for cloning (by being activated by a T helper cell).
clonal expansion - The division of specific B cells to produce genetically identical clones.
primary immune response - This takes place when the body is exposed to a pathogen for the first time. This response is slow and the infected individual experiences symptoms of the disease.
secondary immune response - This takes place when when the body has been exposed to the same pathogen before. This response is much faster and stronger and pathogens are destroyed before any symptoms appear.
autoimmune diseases:
Sometimes the immune system cannot recognise'self'antigens and starts to attack them.
leads to the breakdown of healthy tissues
immunosuppressant drugs can be used
autoimmune diseases
type 1 diabetes
rheumatoid athriritus
lupus
type 1 diabetes - autoimmune disease
immune system attacks the insulin secreting cells of the pancreas