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Adaptive Immunity: Specific Defenses of the Host
Chapter 17 Tortora
Immunity
• Protection against disease (etc)
• The immune system recognizes foreign substances and develops an immune response against them.
• Innate or nonspecific immunity seems to have an inherited (genetic) component
• Adaptive or specific immunity adapts to a particular invader or foreign substance
Types of acquired immunity
• Acquired immunity can be acquired passively or actively
• Active or passive can be acquired naturally or artificially
• Naturally acquired active immunity-exposure to antigens (you get sick and recover)
• Naturally acquired passive immunity-natural transfer of antibodies from mom to child (breast feeding and in utero)-this is short lived.
Immunity continued
• Artificially acquired active-get a vaccination which introduces specially prepared antigens into the body – Doesn’t cause disease but stimulates your reaction
• Artificially acquired passive-introduce antibodies into the body– These are derived from serum so are called antisera – Often inject a horse with antigen and then use the
horse antibody (spider and snake antivenom)
Dual nature of the immune system
• First Nobel prize winner was Emil von Behring who discovered immunity can be passed from one organism to another (now called humoral immunity)
• Scientists later discovered this was due to antibodies (1930’s)
• Cell mediated immunity is governed by lymphocytes
• Humoral immunity (antibody mediated) involves the production of antibody
Humoral immunity
• B cells or B lymphocytes are responsible for antibody production
• This provides resistance to bacteria and viruses and bacterial toxins
• B stands for the Bursae of Fabricius
• Antibody or immunoglobulins recognize different types of antigen
Cell mediated Immunity
• Involves T cells (T lymphocytes) that act against foreign cells or tissue
• T cells mature in the thymus gland• Also regulate the activation and proliferation of
other immune system cells• Cell mediated immune response is directed
against bacteria and viruses inside phagocytic cells or infected host cells, fungi, protozoa, and helminths
• This also causes rejection in implanted tissue
Antigens and antibody
• Antigen is any foreign substance• We recognize ‘self’ and don’t attack it (MHC
antigen)• Antibody is produced by B cells and combines with
antigenic determinant or epitopes on the antigen• Some antigens are small (a molecular weight of
less than 10,000) and won’t trigger a response unless attached to a carrier. These small antigens are HAPTENS.
• The antibody reacts with the hapten, not the carrier.
Nature of antibody
• Antibodies are proteins made in response to antigen that recognize and bind to antigen
• The valence of an antibody is the number of antigen binding sites
• Most humans are bivalent • Antibodies are members of a group of
soluble proteins called immunoglobulins or Igs.
Antibody structure
• A bivalent is the simplest structure for an antibody so it is referred to as a monomer
• A monomer usually has 4 protein chains
• Two of these are identical light chains (L) and two are identical heavy chains (H)
• Light and heavy refer to molecular weights
http://courses.washington.edu/conj/immune/antibody.htmCitation for picture
Antibody structure continued
• Variable regions (V) are located at the end of the Y’s arms
• Their structure reflects the specific antigen they recognize, and these are specific to the two antigen binding sites (bind to epitopes)
• The stem and lower portion of the Y are the constant regions (C)
• These are the same for a particular class of Ig• There are 5 major types of C regions, giving us 5 major
classes of immunoglobulin• The Fc regions (on the stem) are important in
immunological reactions
Classes of Ig
• IgG-80% of all serum antibody, cross blood vessel walls and enter tissue fluids– Cross placenta to protect fetus– Protect against circulating bacteria, viruses, neutralize
toxin, trigger complement, and enhance phagocytic cells
• IgM 5-10% of serum antibody and is shaped like a pentamer– First to respond to initial antigen exposure.
Subsequent exposure results in increased IgG– Valuable in diagnosis because it is early to respond.
Classes continued
• IgA-5-10% of serum antibody, but most common in fluids like saliva and breast milk (helps keep baby safe while it develops its own immune system)– Prevent attachment of viruses and/or bacteria to
mucosal surfaces
• IgD-0.2%, found on surface of B cells and act as antigen receptors (no known function in serum)
• IgE-0.002% of serum antibody, Fc portion binds to mast cells and basophils (allergic reactions), – Increases during parasite or allergy
B cells and Humoral immunity
• This antibody mediated immunity is carried out by B cells
• HOW?• B cell exposed to antigen and become activated• B cells divide and produce clones called plasma
cells• Plasma cells produce antibody to that specific
antigen (say you have measles for instance, it won’t work against chicken pox)
• Some turn into memory cells so that you can have long term immunity to that disease.
More on B cells
• B cells come from stem cells in bone marrow (adult) and liver (fetus)
• Mature B cells are found in spleen and lymph nodes
• Recognize antigen by antigen receptors on cell surface
• Apoptosis-programmed cell death• We make 100 million lymphocytes a day, so
equal number must die. Any that don’t encounter antigen quickly go through apoptosis
Activation of antibody producing clones
• Each B cell can only produce an antibody against a particular antigen
• A mature B cell can have 100,000 IgM or IgD antibody bound to it’s surface
• When antigen binds to antigen receptor, the B cell proliferates into clones that will recognize this one antigen (clonal selection)
• Each B cell has the ability to respond to 100 million antigens thanks to the variable region, but once it has responded it can only make clones for ONE type.
Antigen/antibody complex
• B cells usually require the help of a helper T cell• An antigen that requires the helper T cells for antibody
production is called a T-dependent antigen• B cell contacts the antigen and is processed inside the B
cell• Fragments of the antigen combine with MHC and are
displayed on the B cell surface.• The T cell comes in contact with the antigenic
fragment/MHC presented on the B cell and activates the T cell
• The T cell produces cytokines that in turn activate the B cell to produce clones, some of which become the plasma cell.
Antigen-antibody binding and results
• Antigen/antibody complex is formed quickly• Binding targets the antigen for phagocytosis or
complement• Agglutination is clumping of antigens to make
them easier for phagocytes to digest• Neutralization-IgG antibodies inactivate viruses
by blocking their attachment to a host• Opsonization-antigen is covered by antibody to
aid in ingestion/digestion by phagocytic cells• IgG and IgM trigger complement
T cells and Cell mediated Immunity
• The chemical messengers of immune cells are called cytokines
• These chemical messengers allow the cells to communicate with each other
• There are 60 different cytokines identified to date• Some cytokines help the communication between
leukocytes and are called interleukins • There are 18 of these (IL-1, IL-2 etc) (see table
17.3)• Another group is called chemokines that help
induce leukocytes to migrate into infected areas.
Cellular components of immunity
• T cells are the key component
• They develop from stem cells in bone marrow and mature in the thymus gland
• After maturation they migrate to lymphoid organs
• T cells respond to specific antigen, multiply as clones into effector T cells, and destroy the invader
Types of T cells
• Helper T-have central role in immune response, these activate macrophages and help form cytotoxic T cells
• Cytotoxic T destroy target cells on contact by producing perforin that lysis a bacterial or viral infected cells
• Delayed hypersensitivity T involved in allergic reactions and tissue rejection,
• Suppressor T are involved in stopping the reaction once the danger is passed. (Now called regulatory T cells).
• Another way to classify T cells is by the type of surface receptor called CD (clusters of differentiation)
• Two are CD4 and CD8.
Nonspecific cellular components
• Natural killer cells or NK cells -lymphocytes that can destroy other cells, especially tumor cells and other viral infected cells
• Activated macrophages are stimulated macrophages that have been activated by the cytokines produced by helper T cells
• These macrophages can be activated by digesting antigen too.
• Macrophages often act as antigen presenting cells (APC’s)
• This is identified by the T cells
Interrelationship between cell mediated and humoral immunity
• Antibody production depends on macrophages and T cells (T dependent antigen)
• 1. antigen is ingested and presented by the APC
• 2. The helper T cells reacts with this MHC-antigen complex
• 3. This activates the T cell and it begins to proliferate and produce cytokines.
• 4. The cytokines activate macrophages, CD8 cells, and natural killer cells
continued
• 5. IL-2 influences a B cell to differentiate into a plasma cell that produces antibody
• Sometimes antigen can stimulate B cells directly without the help of T cells. This is called T independent antigen
• In this case the antigen reacts directly with the B cell receptors.
• This is usually weaker
Immunological memory
• Intensity of the antibody mediated humoral response is reflected by antibody titer
• This is the amount of antibody in the serum after infection has been cleared
• There is no detectable titer in the serum for 4-7 days (initial infection)
• IgG peaks in 10-17 days, and titer increases• This is the primary response• If you are exposed again, the memory response
peaks in 2-7 days and is much greater!
When the immune system goes haywire!
• Hypersensitivity-antigenic response beyond the normal response due to previous exposure (sensitization) by an allergen
• 4 types:– Type I-anaphylatic reactions– Type II cytotoxic reactions– Type III-Immune complex reactions– Type IV-delayed cell mediated (delayed
hypersensitivity)– http://www.cehs.siu.edu/fix/medmicro/hyper.htm
Type I
• Occur quickly (2-30 minutes) after exposure• May be localized or systemic• Localized reactions include hives, hay fever,
asthma• Systemic includes shock and breathing difficulty
(death can result)• Over reactive IgE ( you inherit the sensitivity but
may have a completely different allergy)
Type II
• Involve activation of complement by IgG or IgM antibodies within an antigenic cell
• This causes lysis of the cell• Common type II reactions are transfusion
reactions (ABO blood group)• Erthryoblastosis fetalis or hemolytic
disease of the newborn (Rh negative mom has a second Rh positive baby, the second baby is likely to develop this)
Type III
• Form when certain ratios of antigen and antibody occur• Usually involves IgG• IF there is a slight excess of antigen, the soluble
complex that forms is small and escape phagocytosis• It this happens the complex may become trapped in the
basement membrane beneath cells, activating complement and inflammation
• Neutrophils enter and release enzymes that can damage the cells within 2-8 hours.
• An example is glomerulonephritis which damages kidney glomeruli causing kidney failure
• Another is serum sickness following injection of antitoxin produced by an animal
Type IV
• Caused by T cells
• Delay may be a day or more
• Include allergic contact dermatitis (allergic to latex)
• T B tine test