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36 Cards in this Set

  • Front
  • Back

physical/chemical barriers

part of innate (nonspecific) immune system




include tears (contain lysozymes that digest bacterial cell walls)




include mucus secretions and cilia in lungs (that trap and expel particles)




include low pH in stomach which kills bacteria




and includes defensins on skin, which are antibacterial enzymes

complement protein pathways

part of innate immune systems




punch holes in bacterial cell walls in the bloodstream




can be activated by alternative pathway (does not require antibodies)




or classical pathway (uses antibodies bound to pathogens- all pathogens (indiscriminate))

interferons

part of innate immune system




prevent viral replication and dispersion by



-limiting permeability of cells to viruses,


slowing protein production of nearby cells, upregulating MHC1 and MHC2 so there is more antigen presentation




responsible for flu-like symptoms of viral infections

Inflammation

cell-mediated defense




increases heat and blood flow so less hospitable to pathogens




induced by chemical signals released from damaged tissue cells and immune cells already present in tissues including mast cells, macrophages and dendritic cells




alerts immune system that something is wrong

phagocytosis

done by macrophages, white blood cells that eat bacterium (located by pathogenic peptides)

antigen presentation

after broken down in macrophage to smaller polypeptides - MHC binds antigens and carries to cell surface




displayed antigens recognized in lymph or blood by adaptive immune system cells

macrophages

agranulocytes that engulf pathogens




arise from monocytes which are triggered to become macrophages by bacterial invaders in tissues




release cytokines which stimulate inflammation and recruit additional immune cells

Major Histocompatibility Complex Class I

Class I displayed by all nucleated cells




also break down and display normal proteins, so presentation of non-self molecules indicates infection and triggers response




endogenous pathway, binds antigens that originated inside cell

Major Histocompatibility Complex Class II

Class II molecules are mainly displayed by immune cells




exogenous pathway, bc binds antigens that originated outside cell

Natural Killer Cells

not first resort




called in once virus invades cells and manages to downregulate MHC molecules, making it harder for T-cells to recognize infection bc no peptides on cell surface




NK cells detect downregulation and induce apoptosis of infected cells

granulocytes

include neutrophils, eosinophils, basophils




participate in inflammatory response

neutrophils

white blood cells




are short lived phagocytic leukocytes that eat bacteria




follow bacteria via chemotaxis




can detect bacteria that have been opsonized (marked w/ antibody by B-cell)

eosinophils

release histamine (inflammatory mediator) after activation by allergic reactions or invasive parasitic infections




allow immune cells to move out of bloodstream and into interstitial space around injured tissue

basophils and mast cells

release large amounts of histamine in response to allergens




basophils have large purple granules




mast cells exist in mucosa, epithelium (exposed to outside world)

B-cells

govern humoral adaptive immune response




in charge of antibodies




mature in bone marrow, activated in spleen and lymph nodes

antibodies

aka immunoglobulins




specific to microbe's antigens




can be on cell surface or secreted by lymphocytes into body fluids

opsonization

when antibody in body fluid binds to antigen, can attract other leukocytes to phagocytize the pathogen

agglutinization

antibodies can cause pathogens to to clump together to form large insoluble complexes that can be phagocytized

neutralization

antibodies can block a pathogen from invading tissues, essentially neutralizing them, since they can't infect new cells

plasma and memory cells

triggered by B-cells, which are activated when antigen binds to an antibody on surface of healthy host cell from previous infection

mast cells

when antigens bind to antibodies on mast cells, degranulation occurs, release of histamine, inflammatory response

antibody structure

heavy and light chains joined by disulfide linkages and noncovalent interactions




variable region binds only one specific antigen sequence

hypermutation

leads to clonal selection. variable region mutated to find best match for antigen- only B/T cells specific to pathogen are activated

constant region of antibody

allows for initiation of complement cascade- binds natural killer cells, macrophages, monocytes, eosinophils

isotype switching

B-cell changes constant region to bind different effector molecules




stimulated by specific cytokines

naive b-cells

before exposure

plasma cells

B-cells produce after exposure to matching antigen




produce large amounts of one antibody

memory B-cells

B-cells produce after exposure to matching antigen




involved in secondary response, stay in lymph nodes




if microbe seen already reenters, produce antibodies specific to that pathogen

T-cells

mature in thymus by positive selection (cells that can respond to presentation MHC antigen)




or negative selection (causing apoptosis in cells that are self-reactive)

thymosin

regulates maturation of T-cells

Helper T-cells

(CD4+) secrete lymphokines to coordinate immune response




respond to MHC2




loss of these causes HIV




2 types: Th1 release interferon gamma, which activates macrophages)


Th2 help activate B-cells

lymphokines

secreted by helper t-cells, increase activity of other immune cells

cytotoxic T-cells

CD8+ induce apoptosis of infected cells




respond to antigens on MHC1 cells (which are not immune specific)




inject toxic chemicals into virally infected cells

suppressor/regulatory T-cells

help moderate immune response




turn off self-reactive lymphocytes, either by targeting them for destruction or turning into suppressor T-cells




similar to helper T-cells but have Foxp3 gene



Memory T-cells

similar to memory b-cells




more rapid, robust response

allergen path

1st time, B-cells recognize allergen protein, and plasma cells release antibodies




Antibodies activate mast cells




NExt time, mast cells release histamine and cytokines