Please enable JavaScript.
Coggle requires JavaScript to display documents.
Systems of Immunity - Coggle Diagram
Systems of Immunity
-
Cell-Mediated
Immunity
involves
- T-lymphocytes
- operate from lymph nodes
- production of T cells stimulated by body's own cells
- that have been changed due to presence of non-self cells
role
- destroys antigens
within cells
TYPES OF T-CELLS
KILLER
destroy infected cells
- by attaching to antigens on cell
membrane (of infected/abnormal cells)
-
produce perforins
- destroy cell surface
mem of infected cell
- cause lysis
- cell dies
HELPER
stimulate other cells in immune response
- B-cells = produce plasma cells, produce antibodies)
promote process of phagocytosis
- attach special chemicals (opsonins) to pathogen
- mark out for phagocytes
secrete protein interferon
- helps limit ability of virus to replicate
-
SUPPRESSOR
switch off immune response
- after pathogens have been destroyed
-
-
-
definition
- production of T cells
- stimulated by body's own cells
(antigen-presenting cells)
- that have bee changed
- due to presence of non-self cells
antigen presenting cells
- PHAGOCYTES
- CANCER (tumour) CELLS
- any body cells INVADED by VIRUS
Active Immunity
D: individual's own immune system produces
specific antibodies, T cells + memory cells to
particular foreign antigen
-
-
-
Passive Immunity
-
NATURAL
IMMUNITY
placental transfer
foetus receives antibodies from its mother's
circulation across placenta - before birth
colostral transfer
colostrum (first formed milk) rich in antibodies
antibodies absorbed from intestines of new born baby - just after birth
ARTIFICIAL IMMUNITY
- results when antibodies preformed in 1 individual
- extracted + injected into blood of other individual
serum (containing antibodies)
- taken from person recovering from clinical infection
- injected into another person
immunising animals (older method)
- immunised horses w attenuated pathogens/inactivated toxins
- animal produces antibodies
- serum animals given to person
-
monoclonal antibody production
- specific antigen injected into mouse
- specific sensitised + cloned B-lympho. removed
- hybridised w/ cancer cells to
- produces long-lived lymphocytes
- lymphocytes produce required antibodies
- in a fermenter
- over a long time period.
why cancer cells?
- long life qualities
- rapid division
advantages
-
-
-
more ethically acceptable
- mice less close relationship than horse
- mouse only 1 injection
- antibody not continuously removed from animals
SPEED & DURATION
RAPID
- process of B-lympho. sensitisation + plasma cell production - NOT NEED TO OCCUR
TEMPORARY
- antibodies broken down + removed from blood
- immune system not make more antibodies
- ∴ NO MEMORY CELLS present
Lymphocytes
-
-
Lymphocyte Activation
-
when specific immune response occurs
- antigen comes into contact w compl. lymphocyte
- lymphocyte = SENSITISED
B-lymphocytes
- genes activated
- lead production antibodies
T-lymphocytes
- types T-cells produced
- w/ different roles
-
Herd Immunity
- if high enough proportion of pop. = vaccinated
- not vaccinated = less likely catch particular disease
- less likely come into contact w someone who has disease
important
- protect vulnerable in society
- are not vaccinated (medical reasons/new-borns)