How Vaccines Work Flashcards
Immunity
The ability of the human body to protect itself from infectious disease The defence mechanisms of the body are complex and include: Innate mechanisms – non-specific and non-adaptive Acquired systems – specific and adaptive
Innate/non-specific immunity
Present from birth
Includes:
Physical barriers e.g. intact skin and mucous membranes
Chemical barriers e.g. gastric acid, digestive enzymes and bacteriostatic fatty
acids of the skin
Phagocytic cells and the complement system
Enhances the body’s immune response to an antigen
-Adaptive/acquired immunity
Acquired immunity is usually specific to a single organism or to a group of closely related organisms – share common antigens
2 basic mechanisms for acquired immunity – active and passive
Active acquired immunity
How(Active acquired immunity):
Produced by an individual’sown immune system – usually
long-lasting
Involves cellular responses (cell-mediated), humoral
responses (antibody-
mediated) or a combination acting against one or more antigens on the infecting organism
Can be acquired by natural disease or by vaccination
Vaccines provide immunity similar to that provided by the natural infection, but without the risk from the disease or its complications
The Adaptive immune system -CD4 LINEAGE
APCs see antigen They chop it up and present it as peptides with MHC class II to naïve CD4 T-helper cells They then become effector T- cells of 4 basic types
Antibody mediated HUMORAL IMMUNITY
Antibody provides immunity against infection by:
1. Neutralising bacterial toxins, bacterial adhesins and viruses by blocking and binding
to cell-surface receptors = neutralising antibodies
2. Targeting CTLs to infected cells – antibody-dependent cellular cytotoxicity (ADCC)
3. Coating/opsonising pathogens and targeting them for phagocytosis
4. Antibody-antigen complexes activate classical complement cascade which leads to
destruction of pathogens by phagocytosis or bacterial membrane attack
Roles of antibody subtypes in protection
IgM: major role in complement activation – limited
role in neutralisation and induced by vaccination
(primary response) – blood
IgG: systemic (blood, tissues, lymph) – all major
roles (neutralisation, ADCC (antibody-dependant cellular cytotoxicity), opsonisation, complement activation) – induced by vaccination
IgA: principle isotype in secretions at mucosa (gut, respiratory tract, genital) – less potent at opsonising,a weak activator of complement but strong viral neutraliser – can be induced by
vaccination (but needs adjuvants)
IgE – Helminths
IgD – no role
Passive antibody immunisation
Passive immunity = protection provided by the transfer of antibodies from immune
individuals, most commonly across the placenta (IgG) and from breast milk (secretory
IgA)
Protection from cross-placental antibodies are more effective against some infections
(tetanus and measles) than for others (polio and whooping cough)
This protection is temporary – last for a few weeks or months, as neonates are very
vulnerable to disease
Mother should have an up-to-date vaccination profile, in particular MMR – to protect
their child (rubella can damage the foetus irreversibly)
As healthy immune system is dependent on nutritional status, mothers should also
eat well
Cell-mediated immunity
Cell-mediated immunity is provided by effector
lymphocytes (T-cells) of T-helper 1 type (includes
CD8 CTLs)
2 principal classes – each has specific function
1. CD8 T-cells/cytotoxic/killer T-lymphocytes – recognise and destroy infected cells
2. CD4 T-helper cells – activate phagocytic macrophages to destroy engulfed bacteria and activate B-cells to produce IgG1 and IgG2 subtypes – strongly opsonising