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Specific immunity
Adaptive immunity that is acquired after an immunization event
Can be a vaccine or infection
Immunocompetence
The ability of the body to react with countless foreign materials and mount a response to clear it
Immunocompromised
The inability of the body to react with countless foreign materials and mount a response to clear it
Specificity
The fact that immune properties only work against the specific pathogens they are made to fight
Ex: Immune properties related to measles won’t work against the common cold
Memory
The ability of immune cells to be recalled to action once the body is faced with the pathogen they are
Antigens
Anything that can stimulate an immune response
Typically a protein or peptides
Immunogen
An antigen that does stimulate an immune response
Antibodies
“Immunoglobulins”
- Appreciated as IG
Y shaped protein
Present on the surface of B cells, secreted into the blood, or lymph
Triggered by an immunogen
Binds to of antigen epitopes
Epitopes
The part of the antigen that the antibody can bind to
Multiple per pathogen
T cells
Immune cells
Initially form in bone marrow
Develop in thymus
Subdivided
- Helper T cells
- Regulatory T cells
- Cytotoxic T cells (Killer T cells)
Helper T cells
Immune cell
Turns on other immune cells
Have CD 4 markers
Activated by APCs
Interact with MHC II
Regulatory T cells
Immune cell
Down regulates immune response
Have CD4 markers
Activated by APCs
Interaction with MHC II
Cytotoxic T cells
Immune cell
“Killer T cells”
Have CD8 receptors
Interact with MHC I receptors
- On all cells but red blood cells
Act as marauders that test for potential threats and eliminate them as needed
B cells
Immune cell
Developed in the bone marrow
Makes antibodies
T and B Cell Development
Hematopoietic stem cells
Lymphoid stem cells
Immature lymphocytes
Thymic selection
Process to select only the competent T-cells
Done in the cortex of thymus
Development of TCR
Interaction of MHC
Self check
Marker
Part of the T cell
Works with MHC to allows for communication with other T cells
TCR
“T cell receptors” or “Marker”
Developed in the cortex of the thymus
Somatic recombination rearranges the genes that encode the TCR
- Allow for different cells to recognize different things
MHC
“Major Histocompatibility Complex”
Part of thematic selection
Located on other cells
Set of genes that encode the ability for genes T cells to recognize pathogens
Determine if T cells will become helper or cytotoxic cells
- MHC2: Helper and regulatory t-cells, cause CD4 production by TCD
- MHC1: Cytotoxic t-cells, cause CD8 production by TCD
Apoptosis
Programed cell death
Th2
Type of helper T cell
Stimulate B cells and other T cell activation
Th1
Type of helper T cell
Stimulates macrophages and natural killer cells
B cell development
Mature in bone marrow
Positive selection for cells that have normal receptors
Negative selection of B cells that recognize “self”
They then go to the spleen to undergo somatic
recombination
B cell activation without T help
T cell-independent activation
- Only happens with T-independent antigens
- Doesn’t need T cell help
No memory produced
T-independent antigens
Antigens that have repeats on the surface like LPS
- Allows for multiple BCR to bind
BCR
“B-cell receptor”
APC engulfment of pathogen
First step of B-cell activation with T-cell help
Engulfs the pathogen
Degrades the pathogen
Display peptides on MHC II
Activation of helper T cells
Second step of B-cell activation with T-cell help
Stimulates B-cells to grow and divisions
APC
“Antigen presenting cell”
Present antigens to the immune system
- Use their MHC2 receptors to do this
The phagocytic cells
- Dendrites
- Macrophages
Move to lymph nodes once loaded with antigens to activate helper T cells
B cell activation with T help
First step: APC engulfment of pathogen
- Engulfs the pathogen
- Degrades the pathogen
- Displays peptides on MHC II
Second step: Activation of helper T cells
- T cells grow and divide
Third step: T cell activation of B cell
- T cells activate the B-cells
Produces immune memory
MHC II
Complex on B cells
Plasma cells
Immune cells that secret antibodies to fight pathogens
Class switching
The act of immune cells becoming even more specialized
- Happens as a result of somatic hypermutation
Makes antibodies more effective
- More affinity and better breadth
Opsonization
The tagging of pathogens
Neutralization
Binding of pathogens
Stop action
Agglutination
The sticking of multiple pathogens
Stops activity
Makes for easy elimination
ADCC
“Antibody-dependent cell mediated cytotoxicity”
Attaches to pathogen that is two large to be consumed
Signals cytotoxic T cells to come over and releases their cytotoxins into the pathogens
- Death by a thousand paper cuts
Constant region
Part of antibodies, TCR’s, or BCR”s
Are always the same between similar cell types
Variable region
Part of antibodies, TCR’s, BCR’s
Are always different, even between same cell types
Somatic recombination
Part of the development of TCR
Allows for genetic variance between the TCR of T-cells
- T-cells can sense different things
Development of TCR
First stage of thematic selection
T-cells begin to make their receptors
When somatic recombination happens
Interaction of MHC
Second stage of thematic selection
Newly developed TCR interact with MHC to check their functionality
- If can bind then they move on
Self check
Third stage of thematic selection
Makes sure T-cells don’t recognize self as bad
Interlekin 1 (IL1)
A cytokine that is secreted by APC
Stimulates growth of the bound cell
Interlekin 2 (IL2)
A cytokine that is secreted by the helper T cell that received interlekin 1
Stimulates growth of all kinds of T cells
IgG
Type of antibody
Shaped like a Y
Very prominent in the blood stream
Can cross the placenta barrier
IgA
Type of antibody
Shaped like a two Y’s stuck together, bottom to bottom
Very prominent in the secretions
- GI tract
- Respiratory tract
MCH I Receptor
Located on plasma membrane of all nucleated cells
- All cells but red blood cells
Used to declare health or illness of cell
- When healthy “self” proteins are displayed
- When ill “other” proteins are displayed
Cytotoxic T cells read these receptors to determine if they should kill the cell or not
IgM
Antibody class
Produced as part of the inmate immune response