Type II hypersensitivity

Type II hypersensitivity, in the Gell and Coombs classification of allergic reactions, is an antibody mediated process in which IgG and IgM antibodies are directed against antigens on cells (such as circulating red blood cells) or extracellular material (such as basement membrane). This subsequently leads to cell lysis, tissue damage or loss of function through mechanisms such as

  1. complement activation via the classical complement pathway
  2. antibody dependent cell-mediated cytotoxicity or
  3. anti-receptor activity.[1]
Type II hypersensitivity
SpecialtyImmunology

The activation of the complement system results in opsonization, the agglutination of red blood cells, cell lysis, and cell death.[2]

These reactions usually take between 2 and 24 hours to develop.[2]

Examples
DiseaseAutoantibody target
Autoimmune hemolytic anemiaRed blood cells
Goodpasture syndromeGlomerular basement membrane
Graves diseaseThyroid stimulating hormone receptor
Immune thrombocytopeniaPlatelets
Myasthenia gravisMuscle acetylcholine receptor

[3]

An example of complement dependent type II hypersensitivity is an acute haemolytic transfusion reaction following transfusion of ABO incompatible blood.[4] Preformed antibody (predominantly IgM) against donor red cell antigens not found in an individual of a particular blood group (e.g. anti-A IgM in an individual with blood group B), bind to the donor red cell surface and lead to rapid complement mediated haemolysis and potentially life-threatening clinical consequences. Complement-dependent type II hypersensitivity can also occur during the transmission of incompatible maternal antibodies to fetal red blood cells causing hemolytic anemia in the fetus, known as erythroblastosis fetalis.[5][6]

Another example of a complement dependent type II hypersensitivity reaction is Goodpasture's syndrome, where the basement membrane (containing collagen type IV) in the lung and kidney is attacked by one's own antibodies in a complement mediated fashion.[7]

An example of anti-receptor type II hypersensitivity (also classified as type V hypersensitivity) is observed in Graves disease, in which anti-thyroid stimulating hormone receptor antibodies lead to increased production of thyroxine.[8]

However, there are questions as to the relevance of the Gell and Coombs classification of allergic reactions in modern-day understanding of allergy and it has limited utility in clinical practice.[9]

See also

References
  1. "Immunopathology".
  2. Warrington, Richard; Watson, Wade; Kim, Harold L.; Antonetti, Francesca Romana (10 November 2011). "An introduction to immunology and immunopathology". Allergy, Asthma, and Clinical Immunology. 7 (1): S1. doi:10.1186/1710-1492-7-S1-S1. ISSN 1710-1492. PMC 3245432. PMID 22165815.
  3. "Hypersensitivity reactions". Amboss. Retrieved 20 April 2019.
  4. Tinegate, Hazel; Birchall, Janet; Gray, Alexandra; Haggas, Richard; Massey, Edwin; Norfolk, Derek; Pinchon, Deborah; Sewell, Carrock; Wells, Angus; Allard, Shubha (October 2012). "Guideline on the investigation and management of acute transfusion reactions Prepared by the BCSH Blood Transfusion Task Force". British Journal of Haematology. 159 (2): 143–153. doi:10.1111/bjh.12017. PMID 22928769.
  5. Betts, J. Gordon; Young, Kelly A.; Wise, James A.; et al. Anatomy and Physiology – via Openstax.org.
  6. "Hemolytic Anemia". John Hopkins Medicine.
  7. Goodpasture Syndrome at eMedicine
  8. Graves Disease at eMedicine
  9. Descotes, Jacques; Choquet-Kastylevsky, Geneviève (February 2001). "Gell and Coombs's classification: is it still valid?". Toxicology. 158 (1–2): 43–49. doi:10.1016/S0300-483X(00)00400-5.
Classification
External resources

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