Adaptive Immunity
is the 3rd line of defense
The triggering of specialized cells to specifically target antigens of pathogens with the aid of antibodies to create a specific immune response.
Can be activated quickly or prolongedly
Dendritic B & T- Lymphocytes are the main cells
Key components:
Specificity: Targeted response to distinct antigen
Diversity: Recognition of a wide range of antigens
Memory: Rapid and robust response to previously recognized antigens
Self & non-self Recognition: able to identify antigens on body cells and foreign antigens
Innate immunity
The second line of defense
Also known as inflammation, the fast-acting response to damage of cells through the use of chemical mediators and phagocytic WBCs
Antigen
A substance on or in a pathogen that inflicts a immune response
Antibody
Known as immunoglobulins (Ig)
Produced by differentiated B-lymphocytes
Will detect and bind to specific antigens
IgA, IgM, IgE, IgD
Immune cell origins: Lymphoid progenitor
Natural Killer cells
T-Lymphocytes
B-Lymphocytes
Immune cell origins: Myeloid progenitor
Monocytes
Dendritic cells
Granulocytes
Mast cells
T-Lymphocytes
Target cancer and viruses
Mature and differentiate in the Thymus
Have specific receptors that bind to antigens
Requires direct contact with an antigen and then will proliferate and differentiate into:
cytotoxic T-Lymphocytes (direct destruction of antigen-carrying pathogens)
Helper T-Lymphocytes (enhances humoral & cell-mediated immune responses)
Suppressor T-Lymphocytes (inhibits humoral & cell-mediated responses to not be excessive)
Attack the cells that are infected
Humoral Immunity
adaptive immunity that involves that antibodies within the bloodstream
IgG is the most abundant immunoglobulin and only able to cross placenta
Cell-mediated immunity
Cytotoxic T-Lymphocytes are the main part of this
The recognition of cells carrying non-self antigens
Cytotoxic T-Lymphocytes
Attack tumour and viruses
Direct destruction of antigen carrying pathogens
Express CD8
Helper T-Lymphocytes
Enhance humoral and cell-mediated immune responses
Express CD4
Suppressor T-Lymphocytes
Inhibit humoral and cell-mediated immune responses so they don’t become excessive
Dendritic cells
When they come into contact with a pathogen, it will act as a phagocyte and bring the antigens displayed to T-Lymphocytes for identification
APC’s (antigen presenting cells)
B-Lymphocytes
mature in the bone marrow
Migrate to the lymph tissues and are activated when in contact with an antigen, which causes the B-lymphocyte to differentiate into antibody-secreting plasma cells
They identify specific antigens based off a specific receptor, which causes adaptive immunity involving specific antibodies to be produced
The antibodies are known as immunoglobulins
Attack on the outside of the cell through antibodies
Known as effector cells
Natural Killer (NK) Cells
A large granular lymphocyte
When they come into contact with cells they deem a threat (cancer, virus) they will exert their cytotoxic effect through attacking and killing that cell
Granulocytes
Neutrophils (target bacteria)
Esophils (Target parasites)
Basophils (enhance mast cells, important in allergic reactions)
Monocytes
Will differentiate when in the presence of a antigen into a macrophage
Macrophages will engulf the pathogen and display its antigen so T & B-Lymphocytes can identify it
Active (adaptive immunity) Natural
from infection
Passive (adaptive immunity) maternal
comes from mother to fetus through placenta barrier
Only IgG is small enough to transfer
Artificial (adaptive immunity) Passive
antibody transfer
(immunoglobulins given to someone with rabies)
Artificial (adaptive immunity) Active
getting immunization
Apoptosis
programmed cell death after pathogen is destroyed
The ones that don’t are called memory cells
Clonal Expansion
the producing of more cells
Clonal selection
selects what B-cells antibodies best fit the invader and then those cells will go through clonal expansion and then create monoclonal antibodies or the same
Major Histocompatibility Complexes (MHC)
or
Human Leukocyte antigens
Traps an antigen within the cell and transports it to the cells surface so T-Lymphocytes can identify it
MHC I : found on nucleated body cells and detected by CD8 cytotoxic T-Lymphocytes
MHC II : found on APC’s and is detected by CD4 Helper T-Lymphocytes
Neutralization
The bind of a antigen to a antibody resulting in the pathogen unable to infect other cells
clusters of differentiation (CD’s)
T-lymphocytes express clusters of differentiation (CD’s) which our membrane surface molecules used too determine specific function of T-cell subtype
Toxoids
are antigens in the form of exotoxins that have been chemically modified not to cause harm and can be injected to bind to T-Lymphocytes to enlist a immune response
BRM’s Biological response-modifying drugs
These drugs can enhance or restrict the bodies immune response to disease
The three mechanisms:
enhancement or restoration of the hosts immune system defences against the tumour
direct toxic effects on the tumour cells which causes them to lyse or rupture
adverse modification of the tumours biology which makes it hard for those cells to reproduce
immunomodulating drugs (IMD)
a class of BRMS use to treat autoimmune disorders
Antibody titire
how many antibodies are needed per antigen which is why we may need booster shots