Save
Busy. Please wait.
Log in with Clever
or

show password
Forgot Password?

Don't have an account?  Sign up 
Sign up using Clever
or

Username is available taken
show password


Make sure to remember your password. If you forget it there is no way for StudyStack to send you a reset link. You would need to create a new account.
Your email address is only used to allow you to reset your password. See our Privacy Policy and Terms of Service.


Already a StudyStack user? Log In

Reset Password
Enter the associated with your account, and we'll email you a link to reset your password.
focusNode
Didn't know it?
click below
 
Knew it?
click below
Don't Know
Remaining cards (0)
Know
0:00
Embed Code - If you would like this activity on your web page, copy the script below and paste it into your web page.

  Normal Size     Small Size show me how

MICR 386 Midterm

TermDefinition
immunology study of immune system and its responses to invading pathogens/foreign substances
immune system collection of cells, tissues and molecules that respond to infections
immune response coordinated reaction of immune cells, tissues and molecules to microbes and foreign materials
components of immune system lymphatic vessels, primary and secondary lymphatic organs
lymphatic vessels thinly walled vessels through which the fluids and cells of the lymphatic system move through the lymph nodes and ultimately into the thoracic duct where they join the bloodstream
primary lymphatic organs thymus, bones marrow
secondary lymphatic organs adenoids, tonsils, bronchus associated lymphoid tissue, lymph nodes, spleen, intestines, peyer's patches, appendix
innate immunity physical barriers, chemical elements and innate immune cells that act in a protective manner against environmental or infectious agents
adaptive immunity B and T lymphocytes, first encounter of pathogen develops primary immune response involving both, some cells develop into memory cells to recognize pathogen and respond more efficiently during secondary response
surveillance innate and adaptive act together to detect foreign or defective cells, help prevent proliferation of dangerous cells withing body systems
microbes microorganisms that cause disease
macromolecules larger nonliving molecules found in food, drugs and chemicals
cells capable of distinguishing between self and nonself to target nonself
allergic reactions bodys immune system overreacts to substances that are usually not harmful
autoimmune disease body incorrectly identifies self cells as nonself, considered hypersensitivity diseases
laboratory tests used to analyze state of immune system
vaccination public health strategy to boost immune defenses of individual and population
characteristics of innate immunes system unchanging, immediate, nonspecific reactivities, broad range of targets, no memory
unchanging continuous protection without any rearrangement or alteration in response
immediate response occurs within minutes
nonspecific reactivities can be to common component on mutliple pathogens
no memory not improved by repeated exposure
broad range of targets any elements identified as foreign elicits response
physical barriers mucous membranes, cilial hairs, epithelial barriers
muscous membrane trap pathogens and foreign materials
cilial hairs move trapped pathogens out of the respiratory system via sweeping
epithelial barriers skin, GI tract, respiratory tract produce peptides with natural antibiotic function
chemical barriers secretion, sebaceous gland secretion, commensual organisms in gut and vagina, spermine in sperm, acid pH of stomach
secretion tears, siliva and nasal secretion contains lysozymes
sebaceous gland secretions glands deposit sebum that inhibits bacterial growth
commensual organisms in gut and vagina protect from pathogen colonization by reducing pH
spermine in sperm free radical savenger to prevent damage to DNA
acid pH of stomach pathogens ingested cannot survive pH
leukocytes type of white blood cell identify and eliminate foreign invaders several types
phagocytes neutrophils, macrophages, dendritic cells
neutrophils first responding, migrate to site of inflammation and ingest microbes, increasingly segmented as mature 50-70% of cells
macrophages ingest aged neutrophils and bacteria, secrete cytokines to stimulate inflammation and recruit other immune cells 1-6% of cells
dendritic cells found on tissues in contact with environment, serves as link between innate and adaptive
granulocytes neutrophils, eosinophils, basophils, mast cells
eosinophils secrete histamines and free radicals during parasitic infection, mediators of allergic reaction 1-3% of cells
basophils secrete heparin and histamine in response to parasites and allergic reaction <1% of cells
mast cells role in allergy and anaphylaxis, releasing heparin and histamine rich granules, protective role in wound healing, angiogenesis and blood brain barrier function <1% of cells
natural killer cells large granular cytotoxic lymphocytes with no T or B cell receptor fundamental role in surveillance of altered cells
complement protein mark pathogens for destruction
mannose binding lectin (collectin) involved in opsonization of microbes and activation of complement
opsonization process used to tag foreign pathogens for elimination by phagocytes
c reactive proteins (pentraxin) involved in opsonization of microbes and activation of complement system
coagulation factors involved in coagulation of blood and repair of a damaged vessel
responses of innate immunity inflamation and coagulation, phagocytosis
steps of phagocytosis attachment, ingestion, fusion, digestion, release
phagocytosis important method of eliminating invading pathogens activated by recognition of PAMPs
attachment many surface receptors exist to bind to microbes for phagocytosis
LPS receptor lipopolysaccharide of gram negative bacteria initiates inflammatory signal cascade
scavenger receptor family of receptors for wide variety substances therefore wide variety of ligands
mannose receptor exclusive to microbes, acts as pattern recognition receptor for several microbes
N-formyl-methionyl receptor bacteria produce fMLP which has amino terminal N-formylated methionine, recruit inflammatory cells
types of attachment unenhanced, enhanced
unenhanced attachment nonspecific recognition of PAMPs through PRRs 4 previously discussed
enhanced attachment attachment to an opsonized microbe occurs via IgG antibodies, complement or acute phase proteins
ingestion pseudopods surround and engluf microbe electron pump brings protons into phagosome, lowering pH
fusion phagocytes contain lysosomes that travel along microtubules and fuse with phagosome to create phagolysosomes
lysosomes organelle containing proteolytic enzymes
digestion mcirobes are broken down by lysosomal enzymes in phagolysosomes
release residul bodies are released via exocytosis
residual bodies indigestible materials remaining in vesicles
characteristics of adaptive immune system discrimination, diversity, specificity, specialization, memory, self limitation
discrimination ability to discriminate between self and nonself prevents host injury during response
diversity responds to wide variety of microbes and molecules
specificity distinguishes subtle differences among foreign antigens
specialization response is antigen dependent, ensuring optimal defense against each type of microbe
memory enhanced response to microbe following repeated exposures
self limitation cells allow microbe activated immune response to return to basal state
professional antigen presenting cells MHC class 1 and 2 dendritic cells, B lymphocytes, neutrophils and macrophages
nonprofessional antigen presenting cells MHC 1 all nucleated cells
MHC major histocompatability complex
lymphopoiesis differentiation of lymphoid cells from hematopoietic stem cells
t cells cells with T cell receptors help in cell mediated and humoral immunity
helper T cells (TH) express CD4 coreceptors, involved in killing of target cells
cytotoxic T cells (TC) express CD8 coreceptors involved in killing of target cells
TH1 activate macrophages, responsible for cell mediated immunity
TH2 cause mature B cells to become plasma B cells and produce antibodies for humoral immunity
immunoglobulin antibody
b cells prescense of B cell receptor on surface responsible for antibody mediated immunity express B7 and CD40
immature B cell express cell surface IgM
mature B cell express both IgM and IgD on surface
plasma B cell secretes antibodies following antigen stimulation
memory b cell involved in secondary antibody response
IgA high concentration in mucous membranes, acts as neutralizing antibody to prevent antibody attachment to epithelial cells
IgD small amount in blood, no known effects
IgE found on lungs, skin and mucous membranes plays rule in anaphylaxis by releasing histamines and protects against parasites`
IgG 4 subclasses found in all bodily fluids fighting infections only antibody to pass onto placenta and fetus
IgM largest, found primarily in blood and lymoh excellent complement activator
immunogenicity abililty of a substance to induce a humoral/cell mediated immune response
immunogen molecule that has the ability to evoke a specific immune response and can react with the resultant specific immunity
antigens a molecule that can react specifically with either a preformed antibody, immunoglobulin receptors on B cells or T cell receptors
properties of immunogens foreigness, molecular size, molecular complexity, degradability, physical form
foreigness greater the phylogenetic distance greater structural disparity and therefore greater immune response
xenogeneic different species
allogeneic different individuals of single species
syngeneic similar genetics
isogeneic same genetics
molecular size larger the molecule, greater the immunogeneic property
molecular complexity internal molecular complexity is necessary
degradability easily phagocytosed antigens are more immunogeneic
particulate vs soluble particulate is more immunogeneic
particulate aggregates of protein
denatured vs native denatured more immunogeneic due to loss of tertiary structure and therefore different parts of peptide exposed
denatured loss of structural integrity in a protein
haptens small organic molecule that is antigenic but not immunogeneic unless it is attached to large carrier protein
adjuvants substances that enhance the immunogenecity of an antigen when injected into a human without resulting in immune response against it
epitope immunologically active regions of an antigen that bind to an antigen specific T/B cell receptor on lymphocytes or to secreted preformed antibodies
exogenous antibodies soluble antigens that require no antigen processing for detection
epitope characteristics multivalency, immunodominance, acessibility, specificity
multivalency antigens with multiple epitopes that cn be recognized by antibodies
homogenous contains same epitope multiple times
heterogenous expresses different epitopes, resulting in varried immune response
immunodominance antigen that induces a more pronounced immune response
acessibility antibody needs to be able to reach epitope
specificity antiboides can have higher affinity for a certain configuration (acquired by gene rearrangement)
cross reactivity ability of any antibody to react with 2+ antigens that possess a common epitope
herd immunity individuals at risk for disease are protected because disease cannot spread
newly emerging disease lyme (NE US), Hep C (N Africa and S US), Hendra virus (Australia)
re emerging disease west nile (NE US), Dengue (Mexico), thyphoid (India)
active immunity induces humoral or cell mediated immunity and memory follwing exposure to an antigen
natural active follows exposure to infectious disease
artifical active follows vaccination
passive immunity external antibodies give immediate short lived protection
natural passive transfer of maternal antibodies across placenta to fetus
artificial passive concentrated immunoglobulin extracted from pooled serum and injected into susceptible individuals
live attentuated vaccine contain liver virus with reduced virulence so that the virus will cause infection but no disease
live attentuated ex OPV, MMR
killed or inactivated microorganism killed by physical or chemical processes that therefore cannot cause disease
killed or inactivated ex IPV, pertussis
inactivated toxins bacterial toxin is altered to render it harmless so it will not cause disease
inactivated toxins ex tetanus, diptheria
subunit consist only of antigenic component of the pathogen
subunit ex influenza, hep B
antigen shift occurs when different types of influenza viruses infect a single cell
antigen drift occurs when virus accumulates various point mutations
monoclonal antibodies antibodies dervied from single B cell clone and are specific to single epitope on an antigen
polyclonal antibodies heterogenous mixture of antibodies with different affinity produced by many clones of B cells, recognizing multiple epitopes on an antigen
enzyme linked immunosorbent assay used to determine if a particular antibody present in blood via antiserum analysis
structural components of immunoglobulin 2 heavy chains, 2 light chains, interchain disulfide bonds, intrachain disulfide bonds, variable chain regions, Fab region, Fc region, constant chain region, hinge region, domains, oligosacchariides, hypervaraible regions
papain enzyme that cleaves Fc from Fab, leaving 3 segments
pepsin enzyme that cleaves Fc region into fragments up to hinge, remaining fragment is called F(ab')2 region
serum residual fluid when blood or plasma form a clot
isotype phenotypic variation in constant regions that define each class of immunoglobulin
heavy chain isotype gamma, alpha, mu, delta, epsilon
light chain isotype kappa, lambda
allotype occurs in constant heavy and light chain region of specific isotype, slight differences in amino acid sequences of heavy/light chain of different individuals
idiotypes changes in variable region resulting recognition of epitope
one turn/two turn rule states signal sequence with a one turn spacer can join only with a sequence having a two turn spacer
productive rearrangement joining of VDJ segments in phase to produce a VJ or VDJ unit that can be translated in it entirety
nonproductive rearrangement rearrangement in which gene segments are joined out of phase that the triplet reading frame for translation is not preserved
class switching immunoglobulin class switching changes from IgM to other classes, result in antigen stimulation
switch sites conserved motif upstream from
immunocompetent cell mature lymphocyte capable of recognizing specific antigens mediating immun response
affinity maturation increase in average affinity of antibody for antigen during course of immune response or in subsequent exposure
clonal detection apoptosis of immature B cells that recognize self before fully developed
receptor editing immature B cells edit light chain genes to edit receptor
t cell receptor characteristics extracellular domain, transmembrane domain, cytoplasmic domain
extracellular domain heterodimer of either aB or yb proteins
transmembrane domain anchors TCR to cell membrane/CD3 complex
cytoplasmic domain lacks large cytoplasmic domain and heavily relies on CD3 for signal transduction
CD4 monomer of 4 domains marker for helper T cells
CD8 either aB heterodimer and aa homodimer marker for cytotoxic T cells
y-silencers determine commitment to aB or yb on=aB lineage off=yb lineage
pseudogenes nonfunctional gene due to mutation
combinatorial V-J and V-D-J joining generates large number of random gene combinations in TCR and Ig more in Ig due to more variable genes
alternative joining of D gene segments alternative joining of D segments can occur while 1 turn 2 turn rule observed for considerable diversity in TCR but not Ig
junctional flexibility joining of gene segments exhibits junctional flexibility can generate many nonproductive arrangements for both but also increase diversity
N region nucleotide addition nucleotides may be added at junctions to create diversity
somatic mutaions does not occur in TCR to reduce likelihood of generating self reactive t cell influence VJ and VDJ rearrangement on Ig
allellic exclusion only in TCR-B and Ig
CDR-1 located in variable region of TCR and interacts with peptide in MHC peptide complex
CDR-2 located in variable region of TCR and interacts with a reggion of MHC peptide complex
CDR-3 located in D-J region of TCR and interacts with peptide in MHC binding groove
stem cell undifferentiated, self renewing, pluripotent cell which undergoes mitotic division to generate stem cells and progenitor cell
undifferentiated primordial cell that has not assumed the morphological and functional characteristics it will later acquire
self renewing process of giving rise to infinitely more cells of same cell type
pluripotent capable of giving rise to several different cell types
progenitor cell gives rise to several but not all hematopoietic lineages where it loses ability of self renewal
precursor restricted to single lineage
cortical region consists of large number of thymocytes where gene rearrangement and positive selection occurs
thymocytes immature t cells within thymus
corticomedullary junction border between cortical and medullary regions where negative selection occurs
medullary regions low density of thymocytes, site of maturation
positive selection first step of double selection thymocytes interact with APC's
engaged with MHC I CD8
engaged with MHC II CD4
no interaction in positive apoptosis
negative selection second step of double selection some may recognize APCs expressing self antigen complexes
no engagement surivavl
engagment in negative apoptosis
1st wave of yb T cells occur in fetus, migrate to epidermis
2nd wave of yb T cells occur in newborn, migrate to reproductive epithelium
3rd wave of yb T cells occur in adults, migrate to intestinal epithelium, skin, airway tract and uterus
MHC primarily function to bind and present antigenic peptide fragments on cell surface
polymorphic many existing alternative forms
MHC restriction characteristic of T cells that permits them to recognize antigen only after it is processed and the resulting antigenic peptide is displayed in association with class I/II molecule
autoimmune disease abnormal immune response against self
histocompatability recipient can accept grafts from donors with same haplotype even if recipient expresses additional haplotypes recipient cannot accept grafts from donors with haplotyp recepient does not have, even if others are identical
child histone incompatible MHC encodes major histocompatibility antigens that are not identical and therefore cannot accept grafts
MHC I structure heterodimer of 43000 Da alpha chain and 12000 Da beta microglobulin chain alpha chain folds into 3 domains and beta is one
MHC I binding cleft a1 and 2 fold together into it
MHC I distribution expressed on all nucleated cells highly expressed on blood cells
MHC I expression codominant expression moves each cell displays 6 peptides
MHC II structure heterodimer of 34000 Da alpha chain and 29000 Da beta chain each folds into 2 domains
MHC II binding cleft formed by alpha and beta chain
MHC II distribution b cells, macrophages and dendritic cells display
MHC II expression also expressed codominantly, 12 different in humans
irreversible MHC allows for long term display of complexes
antigen dependent MHC loss of peptide from b cells halts MHC presentation at cell surface
self presentation MHC self peptides can be presented mechanism for grafting
antigen processing involves protein degradation and formation of peptide:MHC complex
antigen presentation involves transport of peptide:MHC complexes to cell membrane of APCs
professional APCs cells that express peptide:MHC I complexes and can provide costimulatory signals includes macrophages, b cells and dendrictic cells
nonprofessional APCs express peptide:MHC I complexes and can provide costimulatory signals includes fibroblasts, glia, thymic epithelial, acinor, pancreatic beta and vascular epithelial cells
cytosolic pathway degrades proteins originiating inside cell
TAP transporter associated with antigen processing
endocytic pathway degrades antigens that originate outside the cell
3 signals of t cell activation antigen recognition, costimulatory molecules, pre signal adhesion
CD2 cell adhesion molecule found on surface of T cells and NK cells
LFA-3 cell adhesion molecule expressed on APCs, particularly macrophages
LFA-1 cell adhesion molecule found on lymphocytes and plays key role in emigration
ICAM-1 cell adhesion molecule expressed on APCs
serial tiggering each peptide:MHC complex consequentially engaged with up to 200 TCRs
B7 proliferatory membrane protein found on activated APCs
CD28 protein expressed on T cells that provides cotsimulatory signals
CD22 sugar binding transmembrane potential binds to sialic acid and inhibits B cell receptors signalling
CD45R protein tyrosin phosphate family expressed on B cells and some T cells
AP-70 normally expressed near surface membrane of T cells
Fyn tyrosine kinase, involved in regulation of cell morphology regulaton
Lck tyrosine kinase in t cells, associated with cytoplasmic tails of CD4/8 coreceptors
IL-2 promotes proliferation of differentiation of T cells into effector and memory T cells
endocytic pathway antigen exogenous
endocytic pathway MHC class 2
endocytic pathway recognized CD4+ helper t cells
endocytic pathway presented by professional APCs
endocytic pathway type of response humoral
cytosolic pathway antigen endogenous
cytosolic pathway MHC class 1
cytosolic pathway recognized CD8+ cytotoxic T cells
cytosolic pathway presented by nucleated cells
cytosolic pathway type of response cell mediated
Created by: gfquinn0
Popular Biology sets

 

 



Voices

Use these flashcards to help memorize information. Look at the large card and try to recall what is on the other side. Then click the card to flip it. If you knew the answer, click the green Know box. Otherwise, click the red Don't know box.

When you've placed seven or more cards in the Don't know box, click "retry" to try those cards again.

If you've accidentally put the card in the wrong box, just click on the card to take it out of the box.

You can also use your keyboard to move the cards as follows:

If you are logged in to your account, this website will remember which cards you know and don't know so that they are in the same box the next time you log in.

When you need a break, try one of the other activities listed below the flashcards like Matching, Snowman, or Hungry Bug. Although it may feel like you're playing a game, your brain is still making more connections with the information to help you out.

To see how well you know the information, try the Quiz or Test activity.

Pass complete!
"Know" box contains:
Time elapsed:
Retries:
restart all cards