cell recognition and immune system Flashcards
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