Goodpasture Syndrome

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Is a rare autoimmune disorder targeting glomerular basement membrane causing acute necrotizing glomerulonephritis. It is often accompanied by hemorrhagic interstitial pneumonitis. It is a type II hypersensitivity disorder. The antibodies are targeting the noncollagenous domain of the α3 chain of collagen IV. Cases of Goodpasture Syndrome always presents with glomerulonephritis. Pulmonary hemorrhage is present in two third of the cases. The reason for this is that the glomerular basement membrane is available for antibodies circulating in the blood in the physiologic state. All other basement membranes can only be reached in pathological states. The alveolar membrane is often damaged by e.g. smoking, thus making the basement membrane available for antibodies.

Epidemiology[✎ edit | edit source]

Goodpasture syndrome is a very rare disease. It only affects 1 in a million. It is more common among caucasians. There are no proven correlations with pathogen infections. It is however more frequent during sping and summer.

Females[✎ edit | edit source]

GS is most commonly presented in females around the age of 60. They usually only have glomerulonephritis.

Males[✎ edit | edit source]

GS is most commonly presented in males around the age of 30. They have both glomerulonephritis and pulmonary hemorrhage.

Pathogenesis[✎ edit | edit source]

The antibodies are directed against the globular NC1 domain of the α3 chain of collagen IV. This epitope is present in basement membranes of kidney, lungs, choroid plexus, the uveal tract, the thymus and the cochlea. There is however very rarely that GS patients presents with anything other than glomerulonephritis and pulmonary hemorrhage. Although a few may develop ocular lesions, none become deaf. This is due to the avaialability of the epitope. Glomerular basement membrane is constantly available since glomerular capillaries are fenestrated. This allows the antibodies to react with the basement membrane. Capillary endothelium in alveoli, which have tight junctions, would have to be damaged before antibodies can react with the basement membrane.

Kidney[✎ edit | edit source]

There is a linear binding of IgG along the glomerular basement membrane. The antibodies activate the complement which again recruits neutrophils and macrophages that causes damage to the tissue. This causes disruption of the membrane integrity, allowing larger molecules and cells of the blood to leak out into the urine. The results are proteinuria, hemauria and oliguria.

Immunopathogenesis[✎ edit | edit source]

The autoantibodies are mainly of the IgG1 and IgG4 subclasses, but in one third of the cases IgA and IgM autoantibodies are also present. Even though improvement are directly related to the fall in circulating autoantibodies, the antibodies alone are not able to produce the classical Goodpasture Syndrome. There is also increasing evidence of cell-mediated immunity playing a part in both initiating and maintaining the disease. The mechanism is unknown, but GS is likely to be a T-cell-dependent immune response.

Treatment[✎ edit | edit source]

Goodpasture syndrome is fatal if left untreated. Before the treatment arrived, mortality rate was almost 100%. Death was either caused by end-stage renal failure or pulmonary hemorrhage. Immunosuppressive therapy, intensive plasma exchange to remove circulating autoantibodies and administration of corticosteroids(prednisolone) and cytotoxic drugs(cyclophosphamide) has proven quite successful. Patiens with a creatinine level <500μmol/L had a 100% survival rate after 1 year with this treatment.

Links[✎ edit | edit source]

Related Articles[✎ edit | edit source]

Bibliography[✎ edit | edit source]

  1. "Cellular and Molecular Aspects of Goodpasture Syndrome", Faris Q Alenzi, Mohamed L Salem, Fawwaz A Alenazi, Richard K Wyse. IJKD 2012;6:2-8
  2. "Goodpasture Syndrome" Laura Bergs. CriticalCareNurse vol 25, no. 5, Oct. 2005.
  3. "Robbins Basic Pathology" Kumar et al, 8th ed, p. 507-508.

References[✎ edit | edit source]