2.4 Cell recognition and the immune system Flashcards
What is an antigen?
Cell-surface molecule which stimulate immune response.
Usually (glyco)protein, sometime (glyco)lipds or polysaccharide
Immmune system recognises as “self” or “non-self” enabling identification of cells from other organisms of same species, pathogen, toxins and abnormal body cells
How does phagocytosis destroy pathogens?
- Phagocyte moves towards pathogen via chemotaxis
2.phagocyte engulfs the pathogen via endocytosis to form a phagosome
3.phagosome fuses with lysosome (phagolysome)
4.lysozymes digest pathogen
5.phagocyte absorbs the products from pathogen hydrolysis
Explain the role of antigen-presenting cells (APCs)
Macrophage displays antigens from pathogen on its surface (after hydrolysis in phagocytosis)
Enhancing recognition by T helper cells which cannot directly interface with pathogens/antigens in body fluid
Give 2 differences between specific and nonspecific immune responses
Nonspecific (inflammation, phagocytosis) = same for all pathogens and an immediate response
Specific (B and T lymphocytes) = complementary pathogen and has a time lag
Name the two types of specific immune response
Cell mediated
Humoral
Outline the process of the cell-mediated response
In cell mediated response Complementary T helper lymphocytes bind to foreign antigen on APC. Releasing cytokines that stimulate the clonal expansion of complementary T helper cells by rapid mitosis which become memory cells or trigger humoral response or the clonal expansion of cytotoxic T cells which secrete enzyme perforin to destroy infected cells
Outline the process of the humoral response
1.Complementary T helper lymphocytes bind to foreign antigen on antigen-presenting T cells
2.Release cytokines that stimulate clonal expansion(rapid mitosis) of complementary B lymphocytes
3.B cells differentiate into plasma cells
- Plasma cells secrete antibodies with complementary variable region to antigen
What is an antibody
Proteins secreted by plasma cells, Contains a quaternary structure, 2 ‘light chains’ held together by disulfide bridges, 2 longer heavy chains
Binding sites on variable region of light chains have specific tertiary structure complementary to an antigen
The rest of the molecule is known as the constant region
How do antibodies lead to the destruction of a pathogen
Formation of antigen-antibody complex results in agglutination, which enhances phagocytosis
What are monoclonal antibodies?
Antibodies produced from a single clone of B cells
What are memory cells?
Specialised T helper/B cells produced from primary immune response,remaining in low levels in the blood. They are able to divide very rapidly by mitosis if organism encounters the same pathogen again
Contrast the primary and secondary immune response
Secondary response
Faster rate of antibody production
Shorter time lag between exposed and antibody production
Higher concentration of antibodies
Antibody level remains higher after the secondary response
Pathogen usually destroyed before any symptoms
What causes antigen variability?
Antigen variability is caused by
1.Random genetic mutation changes DNA base sequence
2.Results in different sequence of codons on mRNA
3.Different primary structure of antigens formed as H-bonds, ionic bonds and disulfide bridges form in different places in tertiary structure
4.Different shape of antigen
Explain how antigen variability affects the incidence of disease
Memory cells no longer complementary to antigen so the individual not immune meaning that they can catch the disease more than once
Many varieties of a pathogen so difficult to develop vaccine containing all antigen types
Compare passive and active immunity.
Give examples of both types
Both involve antibodies
Can both be natural or artificial
Passive natural: antibodies in breast milk/ across placenta
Passive artificial: needle stick injections
Active natural: humoral response to infection
Active artificial: vaccination