| Topoisomerase I (human)
| Autoantigen gene || TOP1
| Affected organ(s) || Dermis
| AssociatedDisease(s) || Scleroderma,
| AutoantibodyIg Class || IgG, IgA
| || DR2
| HLA associations ||DR15
| OtherSusceptibilitygenes || lymphoid protein
phatase type 22
Anti-topoisomerase antibodies (ATA) are directed against topoisomerase and found in several diseases, most importantly scleroderma. Diseases with ATA are autoimmune disease because they react with self-proteins. They are also referred to as anti-DNA topoisomerase I antibody (anti-topo I).
Additional recommended knowledge
Epitopes and subtypes
Anti Scl-70 is recognized as one of two major classes of autoantibodies in sclerosis (systemic or scleroderma). The antigen of Anti Scl-70 was recognized as topoisomerase I in 1986 with anti-centromere antibodies constituting the other class. ATA is associated with more severe disease.
Anti-topoisomerase antibodies can be classified according to their immunoglobulin class (IgM, IgG or IgA). IgG-ATA is found most frequently in scleroderma, with IgA being quite common but IgM very infrequent.
Topoisomerase I is an enzyme that relaxes the strain on DNA by nicking and ligating the DNA. ATA inhibits the activity of this enzyme. Since this activity occurs in the nucleus of the cell ATA is a form of anti-nuclear antibody. Scleroderma results from the overproduction of collagen in affected tissues, one study claims that there is an increased density of Topoisomerase I sites in the collagen genes, and that the antibodies may be altering transcription at these loci.
ATA correlates with rapid progression of disease.
In systemic lupus erythematosus ATA are associated with nephritis.
Increases in ATA+ in scleroderma and SLE are associated with increases in serum CTLA4.
HLA-DR2 (DR15 and DR16) are associated with Scleroderma and systemic sclerosis. It has been found that patients with ATA that recognize the ET4 domain of topoisomerase were frequently HLA-DR2,, and in another population study it was found that DR-15 is associated with ATA in systemic sclerosis. In addition to HLA-DR, the protein tyrosine phosphatase, non-receptor type 22 (lymphoid) (1p13.2 - PTPN22), "CT/TT" genotype showed significant association with anti-topo I. The TAP1gene(6p21.3, HLA complex) has also been found in association with ATA+ sclerosis.
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