TYPE
MECHANISM
TIMING · TEST
CLASSIC EXAMPLES
Type I — immediate
IgE · mast cells
First exposure: Th2 (IL-4) switches B cells to IgE, which coats mast cells. Re-exposure cross-links IgE → histamine now, then leukotrienes and eosinophils (late phase).
Minutes; late phase 2–8 h · skin prick test, ↑ IgE, ↑ tryptase after anaphylaxis
Anaphylaxis, allergic rhinitis, asthma, urticaria, food and insect-sting allergy
Type II — cytotoxic
antibody vs fixed antigen
IgG/IgM bind antigen on a cell or matrix → complement lysis, opsonization and splenic removal, ADCC by NK cells — or receptor stimulation/blockade without damage.
Hours to days · direct Coombs, tissue immunofluorescence (linear)
AIHA, ITP, HDFN, acute hemolytic transfusion reaction, Goodpasture, pemphigus, bullous pemphigoid, rheumatic fever, Graves, myasthenia gravis, pernicious anemia
Type III — immune complex
complexes deposit
Antigen–antibody complexes form in blood, lodge in vessel walls, glomeruli and joints → complement activation (↓ C3) → neutrophils damage tissue.
Local Arthus: hours · serum sickness: 5–14 days · granular immunofluorescence, ↓ complement
SLE, poststreptococcal GN, polyarteritis nodosa, cryoglobulinemia, serum sickness, Arthus reaction
Type IV — delayed
T cells, no antibody
CD4 Th1 cells release IFN-γ to activate macrophages; CD8 cells kill targets directly.
48–72 h · PPD skin test, patch test
Contact dermatitis (poison ivy, nickel), PPD, type 1 DM, MS, Hashimoto, Guillain-Barré, GVHD, acute cellular rejection
Mixed patterns
more than one type
Some diseases use several mechanisms together.
Read the dominant lesion
Hypersensitivity pneumonitis (III + IV), SLE (II cytopenias + III nephritis)
Anaphylaxis care
type I emergency
Systemic mast-cell degranulation → bronchospasm, vasodilation, airway edema.
IM epinephrine first; then antihistamines, steroids
Biphasic reaction can recur hours later