cell recognition and immune system Flashcards
(30 cards)
what is an antigen
- cell-surface molecule which stimulate immune response
- usually (glyco)protein, sometimes (glyco)lipid or polysaccharide
- immune system recognises as ‘self’ or ‘non-self’ = enables identification of cells from other organisms of same species, pathogens, toxins and abnormal body cells
how does phagocytosis destroy pathogens
- phagocyte moves towards pathogen via CHEMOTAXIS
- phagocyte engulfs pathogen via endocytosis to form a phagosome
- phagosome fuses with lysosome (PHAGOLYSOSOME)
- lysosomes digest pathogen
- phagocyte adsorbs the products from pathogen hydrolysis
explain the role of antigen-presenting cells (APCs)
macrophage displays antigen from pathogen on its surface (after hydrolysis)
enhances recognition by TH 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 ; immediate
specific (B and T lymphocytes) = complementary pathogen ; time lag
2 types of specific immune response
- cell mediated
- humoral
outline process of cell-mediated response
- complementary TH lymphocytes bind to foreign antigen on APC
- release cytokines that stimulate:
a) clonal expansion of complementary TH cells (rapid mitosis): become memory cells or trigger HUMORAL RESPONSE
b) clonal expansion of cytotoxic T cells (Tc): secrete enzyme perforin to destroy infected cells
outline process of humoral response
- complementary TH lymphocytes bind to foreign antigen or antigen-presenting T cells
- release cytokines that stimulate clonal expansion (rapid mitosis) of complementary B lymphocytes
- 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
- quaternary structure: 2 ‘light chains’ held together by disulfide bridge, 2 longer ‘heavier chains’
- binding sites on variable region of light chains have specific tertiary structure complementary to an antigen
- rest of the molecule known as constant region
how do antibodies lead to the destruction of 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 TH / cells produced from primary immune response
- remain in low levels in the blood
- can divide very rapidly by mitosis if organism encounters the same pathogen again
secondary immune response compared to primary immune response
secondary
- has faster rate of antibody production
- shorter time lag between exposure 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
- random genetic mutation changes DNA base sequence
- results in different sequence of codons on mRNA
- different primary structure of antigen = H-bonds, ionic bonds and disulphide bridges form in different places in tertiary structure
- different shape of antigen
explain how antigen variability affects the incidence of disease
- memory cells no longer complementary to antigen = individual not immune = can catch the disease more than once
- many varieties of a pathogen = difficult to develop vaccine containing all antigen types
examples of passive natural
antibodies in breast milk/across placenta
examples of passive artificial
antivenom, needle stick injections
examples of active natural
humoral response to infection
examples of active artificial
vaccination
passive immunity
- no memory cells and the antibodies are not replaced after breaking down = short-term
- immediate response
- antibodies from external source
- direct contact with antigen not necessary
active immunity
- memory cells produced = long term
- time lag
- lymphocytes produce antibodies
- direct contact with antigen necessary
explain principle of vaccination
- vaccine contains dead/inactive form of pathogen or antigen
- triggers primary immune response
- memory cells are produced and remain in the bloodstream, so secondary response is rapid and produces higher concentration of antibodies
- pathogen destroyed before causing symptoms
what is herd immunity
vaccinating large proportion of population reduces available carriers of the pathogen
protects individuals who have not been vaccinated e.g. those with weak immune system
suggest ethical issues surrounding use of vaccines
- production may involve use of animals
- potentially dangerous side-effects
- clinical tests may be fatal
- compulsory vs opt-out
describe the structure of HIV
- genetic material (2xRNA) and viral enzymes (integrase and reverse transcriptase) surrounded by capsid
- surrounded by viral envelope derived from host cell membrane
- GP120 attachment protein on surface