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4.1.1 Disease
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Herd
immunity
If a significant number of the population are
immune
, even those without immunity are
protected
SKIN
skin flora that competes with
pathogens
a
lower
pH
BLOOD CLOTTING
mesh of
protein
fibres plug up wounds
WOUND
REPAIR
tissue
below
the wound contracts
repaired with
COLLAGEN
fibres
INFLAMMATION
tissue
damage
mast
cells release
HISTAMINES
AND CYTOKINES
redness, swelling, heat and pain
CYTOKINES
attract
phagocytes
for phagocytosis
HISTAMINE
VASODILATION - more blood in area so
increased
temp to kill pathogens
INCREASED
PERMEABILITY
OF BLOOD VESSELS - more tissue fluid pushed out to trap pathogens
NEUTROPHIL
LOBED
nucleus
NO major
histocompatibility
complex
under 10 mins for phagocytosis
MACROPHAGE
ROUND
nucleus
MAJOR
HISTOCOMPATIBILITY
COMPLEX
takes much longer for phagocytosis
PHAGOCYTOSIS - macrophages
non-self pathogen antigen's discovered
phagosome
formed in macrophage
fuses with
lysosome
phagolysosome
formed
hydrolytic
enzymes (lysozymes) digest the pathogen
MAJOR HISTOCOMPATABILITY COMPLEX binds to antigens and presents the antigens on its plasma membrane
ANTIGEN
PRESENTING
CELL formed
cell
mediated response - T-cells
antigen on APC binds to T-cell
CD-4
receptor which is
complementary
clonal selection
T-helper
cell is activated and produces interleukins that stimulate
mitosis
- clonal expansion
T-killer
cells, T-memory cells and
T-helper
cells
T-killer cells
release
PERFORINS
make holes in plasma membranes
apoptosis
T
-helper cells
release
interleukins
that stimulate
phagocytosis
and division of B cells
T-memory cells
remain in circulation to allow a
rapid
response to
reinfection
humeral response - B cells
B cell with antibody complimentary to antigen binds to antigen
OR is activated with
interleukins
from T-helper cells
clonal selection occurs and are activated
B cells divide by mitosis and clonal expansion occurs to form B plasma cells and B memory cells
B
plasma cells
Clones of B
lymphocytes
that produce and recreate specific
antibodies
B memory cells
remain in circulation to rapidly divide into
plasma
cells upon
reinfection
antigen
-antibody complexes allow for
AGGLUTINATION
NEUTRALISATION
OF
TOXINS
OPSINONS
PREVENT PATHOGEN
BINDING
opsinons
increase
likelyhood of
phagocytosis
ANTIBODIES
variable
region - antigen binding sites
hinge
region - flexibility
constant
region - binding to immune cells
disulphide
bridges - hold polypeptide chains together
Primary
response
Slow
clonal
selection +
expansion
Person feels
symptoms
Secondary
response
faster clonal selection and expansion
B
and
T
memory cells are present
B memory
cells divide and a large number of
antibodies
are produced in a short period of time
no
symptoms experienced
rheumatoid
arthritis
Immune system attacks
cells
in the joints
Causing
pain
and
inflammation
Treatment:
No cure
Pain relief
Immunosuppressants
Autoimmune
disease
immune system stops recognising
self-antigens
attacks own
cells
an
abnormal
immune response against
normal
tissues in the body
Lupus
Skin
and
joints
Causes fatigue
Can
attack
any
organ
in body
No cure
Anti-inflammatory
drugs
Immunosuppressants
Type 1 Diabetes
Insulin-secreting
cells in pancreas
Insulin
injections
Immunosuppressants
Pancreas
transplant
Epidemic
– Communicable disease spreads rapidly at local/national level
Pandemic – Communicable disease spreads rapidly across
multiple countries
Preventing
epidemics with vaccines
Mass vaccination
at start of epidemic prevents spread of
pathogen
to wider population
If significant number of population are
immune
, even those without immunity are
protected
This is
herd immunity
Diseases
without vaccines
Malaria
Plasmodium
proctocista spends time in RBCs
So is protected by
self-antigens
HIV
Enters
T-cells
and
macrophages
Disables
immune
system
itself
Some
vaccines need changing
each
year
Eg influenza
:
There are different strains
of the virus
each
year
- immunologically different
So antibody produced
needs to match the new antigen
Personalised
medicine
Medicine tailored to an individual’s
genome
Synthetic
Biology
Synthesis
of new organisms
Genetically
modified organisms to produce a
drug
Medicine
and Biodiversity
Biodiversity is being
reduced
Eg
deforestation
But only a
fraction
of
life
on earth has been investigated by scientists
And we need to make sure we aren’t
destroying organisms
that could provide us with a
life-saving drug
Aspirin
Based on compounds from
willow
bark
Pain killer
Digoxin
Based on digitoxin from foxgloves
Heart drug – to treat atrial fibrillation + heart failure
Risks
of antibiotics:
Side effects
Severe
allergic
reactions
Antibiotic
resistance
Penicillin
was the first antibiotic discovered (Alexander Fleming 1928)
Widely used by mid 20th century to treat bacterial infections
MRSA
– causes serious wound infections
- resistant to
methicillin
C. Difficile – causes diarrhoea, fever, cramps
Tuberculosis (TB)
Bacteria
Animals + humans
Ring rot
Bacteria
Potatoes,
tomatoes
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