2.4 cell recognition and the immune system Flashcards
Antigen
Molecules which, when recognised as non-self, can trigger an immune response and lead to the production of antibodies
Often proteins on the surface of cells
Proteins have a specific tertiary structure allowing different proteins to act as specific antigens
What the immune system identifies
Pathogens e.g. viruses, fungi, bacteria
Cells from other organisms of the same species e.g. organ transplant
Abnormal body cells
Toxins released from pathogens
Phagocytosis of pathogens
Phagocyte recognises foreign antigens on the pathogen and binds to the antigen
Phagocyte engulfs pathogen by surrounding it with its cell surface membrane
Pathogen contained in vacuole in cytoplasm of phagocyte
Lysosome fuses with phagosome and releases lysozymes (hydrolytic enzymes) into the phagosome
These hydrolyse/digest the pathogen
Phagocyte becomes antigen presenting and stimulates specific immune response
Cellular response (T lymphocytes)
T lymphocytes recognise antigen presenting cells after phagocytosis
Specific T helper cell with receptor complementary to specific antigen binds to it, becoming activated and dividing rapidly by mitosis to form clones which:
Stimulate B cells for the humoral response
Stimulate cytotoxic T cells to kill infected cells by producing perforin
Stimulate phagocytes to engulf pathogens by phagocytosis
Humoral response
Clonal selection: in which specific B cell binds to APC and is stimulated by helper T cells which releases cytokines
Divides rapidly via mitosis to from clones
Some become B plasma cells for the primary immune response - secrete large amounts of monoclonal antibodies into the blood
Some become B memory cells for the secondary immune response
Primary response
Produces antibodies slower and at a lower concentration
as not many B cells available that can make the required antibody &
T helpers need to activate B plasma cells to make the antibody
So infected individual will experience symptoms
Secondary response
Produces antibodies at faster and higher concentration as
B and T memory cells present
B memory cells undergo mitosis quicker
Describe and explain how the structure of an antibody relates to its function
Primary structure of protein = sequence of amino acids in a polypeptide chain
- determines the folds in the secondary structure as r groups interact
- determines the specific shape of the tertiary structure and position of hydrogen, ionic and disulphide bonds
Quaternary structure contains 4 polypeptide chains held together by H, I, D bonds
- enables the specific shaped variable region to form which is a complementary shape to specific antigen
- enables antigen-antibody complex to form
How do antibodies work to destroy pathogens
Binds to 2 pathogens at same time, forming an antigen-antibody complex
Enables antibodies to clump pathogens together - agglutination
Phagocytes bind to the antibodies and phagocytise many pathogens at once
Vaccination
Injection of antigens
From attenuated pathogens
Stimulates formation of memory cells
A vaccine can lead to symptoms because some of the pathogens may be live and reproduce and release toxins
Use of vaccines to provide protection
Normal immune response but the memory cells are produced
On reinfection, the secondary response therefore produces antibodies faster and at higher concentration
Leading to the destruction of a pathogen/antigen before it can cause harm
Herd immunity
Large proportion but not 100% vaccinated against a disease
Makes it more difficult for pathogen to spread as more people are immune so fewer in population carry the pathogen
Fewer susceptible so less likely that non-vaccinated will come in contact with disease
Active immunity v Passive immunity
Initial exposure to antigen | no exposure to antigen
Memory cells involved | no memory cells involved
Antibody is produced & secreted by B plasma cells | antigen introduced into body from another organism
Slow, takes time to develop | fast acting
Long term immunity > antibody can be produced in response to a specific antigen again | short term immunity (antibody broken down)
Ethical issues associated with the use of vaccines
Tested on animals before use on humans > animals have a CNS so feel pain
Tested on humans > volunteers may put themselves at unnecessary risk of contracting the disease because they think they’re fully protected
Can have side effects
Expensive - less money spent on research and treatments of diseases
Antigen variability as explanation for why
New vaccines against a disease need to be developed more frequently e.g. influenza
Vaccines against a disease may be hard to develop or can’t be developed in the first place e.g. HIV
May experience a disease more than once e.g. common cold