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strategy of the adaptive immune response
first response to an antigen → primary response
may take a week or more to develop
immune system remembers pathogen on subsequent exposure → secondary response
gets rid of the pathogen before you even know you encountered it
vaccine exploits phenomenon of immunologic memory
for long term protection, very important: memory B cells will differentiate into plasma cells → rapid production of antibodies
strategy of the adaptive immune response - humoral and cell-mediated immunity*
adaptive (acquired) immunity divided into
humoral immunity
eliminates extracellular pathogens
mediated by B cells
mature in bone marrow
*some become plasma (b?) cells that produce antibodies
some become memory cells
allows rapid secondary response if encounter antigen again
cell-mediated immunity
eliminates intracellular pathogens
mediated by T cells
mature in thymus
cytotoxic T cells, helper T cells, regulatory T cells (suppressor T cells)
for every T cell that is stimulated by a specific antigen, there’s a B cell that produces specific antibodies
overview of the adaptive immune response
both parts work together to produce a strong immune response

the nature of antigens
antigen
antibody or generator
any compounds that elicit an immune response (immunogen) → antibody production
epitopes
antigenic determinants on surface of microbes that trigger response
macromolecules
proteins, lipids, and polysaccharides

the nature of antibodies
antibodies also called immunoglobulins
structure
four chains of amino acids held together by disulfide bonds
Y-shaped proteins with two general parts
constant region (Fc region)
variable region (Fab)
unique to each Ab
recognizes and binds to a specific Ag

the nature of antibodies - protective outcomes of antibody-antigen binding
neutralization
prevents toxins, viruses from binding
immobilization and prevention of adherence
binding to bacterial flagella or pili
cross-linking
clumping of bacterial cells by specific antibody
enhances phagocytosis
opsonization
enhances phagocytosis

the nature of antibodies - Ab divided into 5 classes
based on constant region of the antibody
IgM
IgG
IgA
IgD
IgE
five classes of antibodies - IgM
pentamer
first Ab produced in primary response to infection
more forgiving (recognition is less specific)
only Ab that can be formed by the fetus

five classes of antibodies - IgG
second to be produced
most protective and most specific
most abundant Ab in blood (80-85%) and long lasting
only Ab that can cross the placenta and found breast milk
last 6 months to several in child
the antibody of memory ⭐

five classes of antibodies - IgA
most form dimer
found in secretions, important in mucosal immunity
found in breast milk, mucus, tears, and saliva

five classes of antibodies - IgD
help in maturation of antibody response (IgG)
function well not understood

five classes of antibodies - IgE
barely detectable in circulation
active in allergic reaction → produces histamines
tightly bound via Fc region to basophils and mast cells
allows these cells to detect, respond to antigens

clonal selection and expansion of lymphocytes
antigen in body → antibody production
process called clonal selection
B cell bind antigen, divides and
differentiate into plasma cells → produce lots of antibodies
become memory cells
responsible for secondary response
without sustained stimulation, cells undergo apoptosis


The B-Cell Response: Humoral Immunity
Primary Response
occur after first encounter with antigen
takes 10-14 days for substantial antibody accumulation
activated B cells divides and become plasma cells as long as antigen is present
net result = increase in antibody titer
Secondary Response
occurs after subsequent exposures
fast, more effective response due to memory cells
pathogens usually eliminated before causing harm
vaccine exploits this natural phenomenon of immunologic memory

T Cell Response: Cell-Mediated Immunity
involves T cells
two types: cytotoxic T cells and helper T cells
interact directly with target cells
never produce antibodies

Two major T cell populations - Cytotoxic T Cells
have CD8 marker
activated by dendritic cells
recognize antigen display by MHC class I cells (all nucleated cells)
release of proteases and perforin to induce apoptosis
destroy infected or cancerous “self” cells


Two major T cell populations - Helper T Cells
have CD4 marker
recognize antigen presented on MHC class II from antigen-presenting cells (APCs)
orchestrate immune response
activate B cells and macrophages
stimulate other T cells

Natural Killer (NK) Cells
induce apoptosis in abnormal “self” cells
recognize foreign proteins on cell membrane bound by antibodies
bind, deliver perforin - and protease - containing granules to cell, initiating apoptosis
also recognize host cells lacking MHC class I
some viruses interfere with antigen presentation
