Chapter 15
Adaptive Immune Response
Matures and Changes throughout a lifetime
Adaptive immunity - protection provided by these immune responses
involves B and T cells
Take a while to build a specific defense following exposure
Innate immunity protects during that time
Adaptive immunity has memory
memory - greatly enhanced response to re-exposure
principle behind vaccination
has molecular specificity
Immune system can discriminate between healthy and non-health self so as not to continuously attack itself
Autoimune disease caused when function is broken
re-infection by the same agent is usually. result of avoiding host defenses not a lick of response
Strategy of the Adaptive Immune Response
Types of Response
Primary
first exposure takes the adaptive immune response aprx. a week to develop, leaving protection to innate immunity
Secondary
enhanced, does not take long
strategies
Humoral Immunity - attempts to eliminate extracellular antigens
bacteria, toxins, or anything in bloodstream or tissue fluids that shouldn't be there like viruses
Cellular Immunity - attempts to eliminate antigens that have infected a cell such as a virus
Immune response is tightly regulated so no unnecessary damage is done
Humoral Immunity
B-lymphocytes (B cells) are the major players
Extracellular antigens trigger B-cells to multiply and differentiate into plasma cells
Plasma cells produce antibodies - Y-shaped proteins that bind a specific antigen
Some B cells form memory B cells - live a long lime as a 13 Cen making it possible to launch a quick response upon re-exposure
Antibodies have two parts
Two identical arms that bind the antigen
the amino acid sequence is variable
Yields specify
Antibody binding protects by preventing an antigen from binding its target by flagging down phagocytes to get rid of the bound molecule (opsonization)
Each B cell carries B-cell receptor which is a membrane-bound derivative of the antibody it is programmed to make.
Binding of the antigen to the B cell
allows it to multiply.
lots of 13-cells or made during the initial response, but only ones that replicate are the ones that can bind the antigen
• 1B cell needs a TH cell to confirm antibody is dangerous clonal selection and expantion of Lymphocytes
clonal selection-process by which a given antigen binds to the specific antigen receptor on a lymphocyte (B at T ang
• Albus cell to proliferate generating clones of its sent
• cornal expansion
target (a teaching) and
Nature of Antigens
Antigen-anything that reacts with an antibody or binds an antigen receptor on a lymphocyte
can be, Microbes, Microbe products, plant pollen Imminogen-antigen that elicits an immune response
can set differing immune responses-
protiens and poly saccrides tend to get a Stronger respons than lipids and nucleic acids
Antigen and Immunogenitic are interchangable
Antigens are large molecules
• certain regions are recognized
• * Antigenetic determinants / epitopes Antigens are also called immunoglobins Two arms called fab regions bind the antigen
Stem is fc region enlists other parts of Immune system
There are two heavy chains and two light chains
Disulfide bonds (S-5) join chains
5 classes of antibodies - human imminoglobins
• Ism, IgG, = IgA, = TSD,ISE =
• distinguished by the stem region
Antibodies
variable Region
• Areas of antigen binding ends of Fab regrong, Differing amine acid sequence
• Area specific for binding its antigen
• binds using many non-covalent interactions binds strongly but is reversible leaving the two molecules unchanged
Constant Region
• All FC region and part of the light and heavy chains in fab regions
• same for all molecules ot a given class
• Talks to other components of the immune system
outcomes of Antibody Antigen Binding
Neutralization
• A toxin or virus normally needs to bind the cell surface to begin to cause
damage
• cannot perform if coated
Immobilization and Prevention of Adherance
• Binding to flagellum and pili prevent motility or attachment
• If these function are essential
• protect host
Agglutination and Precipitation
• Marry antibody /antigen binding interections can secur forming large complexes
• can gather together disperse antigens and have them engulfed simultaneously by phagocyte
• can precipitate solvable antigens
opsonization
• Molecules can bind an antigen making it easier for them to be engulfed
• Ig G molecules
• macrophages and neutrophiles have receptors for fC region of this antibodies
complement system Activation
• Antibody Antigen bilding can trisser the classical pathway of the component system Antibody-dependent Cellular Cytotoxixity
• multiple Ig G binding to a cell becomes targeted for destruction by certain cells like natural killer cells
Immunoglobin classes
Have same basic monomeric structure
Each class has different constant region of
heavy chain
some form multimers of basic monomeric structure
Each Class has distinct functions and properties
Immunoglobin M-Ig M
• 5%-13% of circulating antibodies
• first class produced in response to
T- independent antigens
• pentameter LP binding sites) good at agglutination,
precipitation large
• ussualay can't get into tissues so pimarily for bloodstream infections
• most efficient class for initiating the classical pathway
Immunoglobin G (IgG)
• 80%-85% of total
• in blood, vessels, and tissues
• around longest - 21 days half life
• first and most abundant class during secondary
Immune response
• protect by neutralization, aggulatination, opsonization, complement activation, ADCC
• only class that can cross placenta
• maternal IgG antibodies protect newborns for
3-6 months due to bug half life
• Available in colostrum
Immunoglobin A (ISA)
• 1000-13% of total-most abundant class
made, not in blood
• most secreted, dimer, secretory IgA
• secreted form in mucors membranes and
saliva, fears, and breast milk
• protection due to direct binding-neutralization and preventing attachment
Immunoglobin D Ig D
• less than 10 total
• Development and maturation of the antibody response
• Don't really know yet
Immunoglobin E- IgE
• barely detectable
• not free circulating, f region bound to
mast cans and basophiles
-Antigen binds Ise Molecule and attached cell releases Chemicals like histamine, cyto vines, and compounds that elicit the infurmatory response -Thoughts to be important in parasite elimination
- Allergies pear when bound Ise encounters harmless material like dust and pollen
Primary response characteristics
following first exposure, it takes 10 days to two
weeks to get detectable levels of antibody in the blood
Everything is going on at this time
• Naieve B cells bind antigen and present it to TH cells. Binding results in B-cell activation and proliferation
• some continue to divide and some differentiate into plasma cells secreting thousands of antibodies
B cells undergo changes to enhance the
immune response
formation of memory cells
• some B cells swich to long lived memory cells
• years
• Give fast and effective secondary response
• can live without antigen binding
Secondary Response characteristics
second encounter with particular antigen
significantly faster, more effective than the
primary response
Pathogens usually eliminated before causing harm
vaccination relies on this
memory B cells responsible
more cells are able to respond to the
reinfecting antigen
• 13 cells and resulting antibodies are good at binding the antigen and an effectively
respond to even low levels of antigen
Strategy of Adaptive Immune Response
cellular Immunity
• T lymphocytes (T cens)
• Cytotoxic T cells and helper Tens
• Both have surface moleute - T cell receptor- enabling the cen to recognize a certain antigen.
• Does not recognize free antigen, must be presented by bodies own cells
• T cells form memory cells
• regulatory T cells (T Suppressor cells)- prevent immune system from responding to
healthy 'self' cells
• Both types of T cells must be activated before they can multiply
• Activated by dendritic cells
- After binding, T cells proliferate and differentiate but require another moteale to confirm the antigen is dangerous
• Dendrite cells Cinnate immunity) provide second opinion
• T cells differentiate into effector cells
• effector helper T cens - contribute to humoral and cell mediated immunity activates B cells and meeophages and stimulate other T cens as well as other immune responses
• Effector cytotoxic T cells-responds to intracenular antigens: induces apoptosis to destroy infected or aneerous
self cells
Natural Killer cells
come from lymphoid stem cans
Augment adaptive immune response
Do not have antigen binding receptors
Antibody dependent cenular toxicity - kills cells bound
• "antibody
NK cells have fc receptors for IgG antibodies
when multiple receptors on NK surface bind the
Fe regions the NK can delivers perforins and proteases to the targeted can inducing apoptosis
NK cells can also will host cells that do not have MetH class I protiens on their surface and are under stress
• lack of MCH Class I complex not normal
• other indicators of stress appear on surface
• Important because it is a sign a virus has
circumvented antigen presentation
Anatomy of Lymphatic system
lymphatic system-collection of tissues and organs that brings B and T cells in contact with all antigens that enter the body
ensures appropriate lympocyte encounters it's antigen
1. vid flows through lymphatic vessels
oxygenated blood travels through the heart and longs and through the apilaries.
Fluid from blood filters out into surrounding tissues carrying oxygen and nutrients
fluid reabborbs into epilarries on way back
to heart and lungs
some enters the lymphatic vessels that already contain white blood cells and antigens All travels to lymphmodes where all protien and cell material are removed and lymph empties into Capilaries
Primary Lymphoid organs
• bone marrow and thymus
• where stem cells mature into B and T cells
Secondary Lymphoid organs
• lymph nodes, spleen, tonsils, adenoids, appendix
• stratisec locations for immune response
-sites were adaptive Immune responses are innitiated
• facilitate interactions and transfer of atokines between ans of Immune systeme
• lymphocyts can gather contact various antigens
Lymphocyte Development
1. cells bone marnow
2. cells-Thymus
Generation of Diversity
Impersise Joining
various segments are joind during recrangement
nucleotides can be deleted or added between
sectors, changing the reading phrame
Two Breen have same combination but
diffent antibody
combinatorial Assosiations
Antibody binding Sites are made of light chains and
heavy chains of which contribute to diversity
• Both acquire diversity through rearangement and impercise joins
• They are then combined