What is hypersensitivity?
Immunological responses with excessive or undesirable consequences >>> that may result in tissue or organ damage
Types of Hypersensitivity
5 types:
Who did classify hypersensitivity into 4types in 1963?
Gell and Coombs
Names of different types of hypersensitivity
Type-I hypersensitivity: Main pathophysiology
Importants are >>>
Antigen binds to IgE bound to mast cells > degranulation > histamin release
Type-I hypersensitivity: Mechanism
Allergen >>> Antigen presenting cell (APC) presents the allergen on its surface >>> Th2 recognises it >>> releases IL-4, IL-5 >>> they activate B-cells >>> B-cells become plasma cells (class-switching) >>> releases IgE antibody >>> IgE (through its Fc portion) binds to mast cell and basophil >>>
When re-exposue, Antigen binds to Fab portion of IgE >>> Then, Mast cells >>
>>> smooth muscle contraction, vasodilation & increased permeability
>>> Bronchospasm, Urticaria, Anaphylactic reaction
Type-I & type IV hypersensitivity: Time period
Immediate (within 24hours)
Delayed (after 24hours)
Type-I hypersensitivity: Types
Immediate hypersensitivity has 2 divisions:
Type-I hypersensitivity: Examples
Type-II hypersensitivity: Main pathophysiology
Direct antibody-driven cytotoxicity
(IgG or IgM binds to antigen on the cell surface >> cell destruction)
Type-II hypersensitivity: Mechanism
Target cells have surface antigens >>> Antibodies bind to that surface antigens (with Fab portion) >>> 3 consequences:
Type-II hypersensitivity: Examples
Type-III hypersensitivity: Main pathophysiology
Immune complex deposition
Free antigen and antibody (IgG, IgA) combine
Type-III hypersensitivity: Mechanism
Phase-I: immune complex formation:
Free antigen in the circulation >>> Antigen binds on the surface of B cells >>> B cells becomes plasma cells (Class-switching) >>> releases specific antibody IgG >>> IgG bind to antigens (through Fab portion) >>> Formation of ‘immune complex’
Phase-II: Immune complex deposition:
Phase-III: Immune complex mediated inflammation:
Type-III Hypersensitivity: Examples
Type-IV hypersensitivity: Main pathophysiology
Cell mediated (T cell driven/mediated)
Type IV hypersensitivity: Main goal
Early elimination of responsible agent
Type-IV hypersensitivity: Mechanism
Sensitization phase: (1-2 weeks after primary contact)
Pathogen/foreign body >>> APCs (Macrophages, Langerhans cells) recognise & presents antigen to T-helper cells >>> releases IL-12, IL-6 >>> activates CD4+ T-helper cells >>> Further activation of type-I T-helper cells (Th-1): generally (Occasionally CD8+ cytotoxic T cells)
Effector phase:
Sensitised (Effective) Th-1 cell produces IFN-gamma (also TNF-beta, IL-1, IL-2, IL-8, MCAF, GM-CSF, MIF) >>> resting macrophage >>> Activated macrophage >>> Effect of macrophage activation: high MHC/HLA class II, TNF receptor, oxygen radicals, Nitric oxide, lysosomal enzymes >>> tissue damage
Type-IV hypersensitivity: Examples
(BCG = Bacille Calmette-Guerin)
Type-V hypersensitivity: Main pathophysiology
Stimulating/Inhibiting
(Antibodies stimulate cells they are directed against)
Type-V hypersensitivity: Mechanism
Antibody >>> binds to cell surface receptors (instead of cell surface) >>> either:
Type-V hypersesnsitivity vs Type-II hypersensitivity
Some suggests type-V to be under type-II hypersensitivity
But most suggests it to be an independant type (type-V), because >>>
Type V hypersensitivity: Examples
Grave’s disease
Myasthenia gravis
Antibody types in Type I, II, III, V hypersensitivity