membrane and cytoplasm of phagocyte move around the pathogen, engulfing it. This can be made easier by opsonins - molecules in blood that attach to foreign antigens to aid phagocytosis.
pathogen now contained in a phagosome (vesicle) in cytoplasm of phagocyte.
a lysosome fuses with phagosome to break down pathogen.
phagocyte then presents the pathogen's antigens. It sticks the antigens on its surface to activate other immune system cells. Phagocyte is acting as an antigen-presenting cell
neutrophils
first WBC to respond to a pathogen inside the body.
neutrophils move towards a wound in response to signals from cytokines (proteins that act as messenger molecules).
cytokines are released by cells at the site of the wound.
phagocytes activate T lymphocytes
their surface is covered with receptors
the receptors bind to antigens presented by APCs
each T lymphocyte has a different receptor on its surface.
when the receptor on the surface meets a complementary antigen, it binds to it. Each T lymphocyte will bind to a different antigen.
this activates the T lymphocyte - clonal selection
the T lymphocyte undergoes clonal expansion. It divides to produce clones of itself.
T lymphocytes activate B lymphocytes
they're covered with antibodies
antibodies bind to antigens to from an antigen-antibody complex.
each B lymphocyte has a different shaped antibody on it surface.
when the antibody on the surface of a B lymphocyte meets a complementary antigen, it binds to it. Each B lymphocyte binds to a different antigen.
This with substances released from T helper cells activate the B lymphocyte. This is also clonal selection.
The activated B lymphocyte divides by mitosis into plasma & memory cells. This is also clonal expansion.
plasma cells make more antibodies to a specific antigen
plasma cells are clones of B lymphocyte
secrete lot of the antibody specific to the antigen, into blood
these antibodies will bind to antigens on surface of pathogen to form lots of antigen-antibody complexes.
antibodies
glycoproteins made of 4 polypeptide chains
2 heavy chains, 2 light chains. Each chain has a variable region & a constant region
variable regions of antibody from antigen binding sites
shape of variable region is complementary to a particular antigen. Variable regions differ between antibodies.
hinge regions allow flexibility when the antibody binds to antigen
constant regions allow binding to receptors on immune system cells. It is the same in all antibodies.
disulfide bridges hold the peptide chains of the protein together.
agglutinating pathogens
each antibody has 2 binding sites
antibody can bind to 2 pathogens at the same time
pathogens become clumped together.
phagocytes bind to antibodies and phagocytose a lot of pathogens all at once.
antibodies that behave in this way are known as agglutinins.
neutralising toxins
toxins have different shapes
antibodies called anti-toxins can bind to toxins.
this prevents the toxins from affecting human cells
toxins are neutralised
the toxin-antibody complexes are also phagocytosed.
Preventing the pathogen binding to human cells
when antibodies bind to the antigens on pathogens, they may block the cell surface receptors that the pathogens need to bind to the host cells.
This means the pathogen can't attach to or infect the host cells.
When a pathogen enters the body for the first time, the antigens on its surface activate the immune system
The immune response is slow initially because there aren't many B lymphocytes that can produce the necessary antibody
The body eventually produces enough antibodies to overcome the infection, but the person will show symptoms in the meantime
After exposure to an antigen, both T and B lymphocytes produce memory cells that remain in the body for a long time
Memory T lymphocytes remember the specific antigen and will recognize it
Memory B lymphocytes record the specific antibodies needed to bind to the antigen
The presence of memory cells means that the person is now immune to that specific pathogen
Define the term parasite [3]
lives in / on host
gains nutrition from host
at the expense of host
bacterial diseases
tuberculosis
bacterial meningitis
ring rot
viral diseases
HIV/AIDS
influenza
TMV
protoctist diseases
Malaria
tomato/potato blight
fungal diseases
black sigatoka
ringworm
athlete's foot
neutrophil specialisations
specific receptors
well-developed cytoskeleton
many lysosomes
many mitochondria
lobed nucleus
Outline the processes that lead to the production of antibodies against an unfamiliar bacterium.
B cells have antigen receptor on surface complementary to only one antigen