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Two ways pathogens can evolve
muation or recomination
mutation
rapid replication means lots of chance for mutation
recombination
RNA segment recombination creates changes that can jump speciea
antigenetic shift
virulence strategy where some pathogens alter surface protiens to stay undetected
Adaptive immune systemm
slow, specific and has memory
innate immune system
fast, no memory and not specific
role of innate immune system
to fight colonies that grow faster then the adaptive can fight. via barrieres, cell intrinsic responses and specialised proteins.
mucus layer
protect against microbial, mechanical and chemical attacks via slipperiness, cilia and mucins
defensins
very toxic antimicrobial peptides with domains. can cause lysis. dont harm human cells as they contain cholesterol
complement system
if pathogens breach epithelial barrier it can recognize them via its soluble receptors
Toll like receptors
transmembrane protein with a large extracellular domain and repeating motifs. causes transcription when pathogens are detected
neutrophils
most common phagocyte. short lives and abundant in blood but not healthy tissues
macrophages
larger and longer lives phagocytes. recognize, remove and ingest dead and damages cells
eosinophils
help destroy parasites and modulate allergic reactions
granules
dense, membrane bound lysosomal derivatives which fue with phagocyte membranes and release contents.
inflammation
aids the killing frenzy by swelling blood vessels and causing component accumulation. can lead to sepsis
natural killer cells
persuade infected cells to apoptosis
lymphocytes
type of white blood cell in adaptive
dendritic cells
link innate and adaptice immune system
T- cells
thymus cells, three types cytoxic, helper and regulatort
cytoxic t cells
kill infected host cells
helper t cells
active macrophage, dendrites and maintain cytoxis
regulatory
inhibit function of others
b-cells
recognise soluble antigens, activity mitosis and colonal expansion of specific b cells
antibodies
tetrameric, 4 polypeptide chains, 2 heavy 2 light
Ig M
most primitive, has 5 bonding sites and is a pentameter with a joining chain
Ig G
standard 2H 2L and very abundant
Ig A
dimer (2 tetrameric) held by joining and sectraotry chain
Ig E
triggers degranulation and has receptors for eosinophils
Light chain
V2-C2
Heavy chain
Vh-Ch-hinge-Ch2Ch2-(Ch4)
class switching
somatic recombiantion leads to diversity which leads to class switches as loops are deleted
clonal expansion
to produce more pathogen specific lymphocytes when a pathogen is detected.