Connective Tissue Diseases

Single Analytes 2

Autoantibodies against

ssDNA | Histones (IgG/IgM) | Scl-70CENP | Jo-1 

 

 

ssDNA

Product

Article No.

No. of tests

Varelisa ssDNA Antibodies 148 96 96 tests

Antigen

In 1971 Cohen et al. proposed three categories of antibodies directed against the DNAmolecule:

  • The first category is directed against conformational epitopes associated with the native doublehelical structure. By definition these DNA antibodies are the only true dsDNA antibodies. However, they seem to be rare.
  • The second group targets the polymers of purine and pyrimidine bases, which as antigens are accessible to the immunocompetent cells only in the singlestranded DNA, i.e. in the denatured state. These antibodies are considered the only true ssDNA antibodies.  
  • The third group targets the desoxyribose-phosphate backbone, which is equally present in ssDNA and dsDNA molecules. Accordingly they are neither true dsDNA nor ssDNA antibodies. The majority (85 to 95%) of DNA antibodies in patient samples belongs to this category.

From a technical point of view it is impossible for a single test to measure in a single test true ssDNA antibodies (with purine and pyrimidine bases being the sole antigen). All ssDNA antibodies tests measure DNA antibodies belonging to category 2 and 3. ssDNA antibodies are commonly found in SLE and drug-induced lupus (DIL). Together with histone antibodies and in the absence of dsDNA antibodies they may be an aid in the diagnosis of DIL. However, they are not specific but occur also in systemic and localized scleroderma, liver disorders, a number of connective tissue diseases and some normal individuals.

In the Varelisa assay the plate is coated with synthetic single stranded DNA.

When is the measurement recommended?

Suspicion of SLE or drug-induced lupus.

Antibody isotypes

IgG

Detection methods

Enzyme-linked immunosorbent assays (ELISA).

References

  • Takehara K et al. Anti-Single-Stranded DNA Antibody and Muscle Involvement in Localized Scleroderma. Arch Dermatol 1990; 126:1368-1369
  • Ruffati A et al. Prevalence and Characteristics of Anti-Single-Stranded DNA Antibodies in Locolized Scleroderma.
  • Lange A. Evaluation of the simultaneous estimation of anti-dsDNA and anti-ssDNA antibodies for clinical purposes. Clin Exp Immunol 1978; 31:472-481

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Histones

Product

Article No.

No. of tests

Varelisa Histone (IgG/IgM) Antibodies 164 96 96 tests

Antigen

As an autoimmune disease SLE is characterized by a complex clinical picture and by a great diversity of autoantibodies. Antibodies against dsDNA and RNP-Sm are the most prominent ones in the diagnosis of SLE since they demonstrate high specificity for the disease. Of comparable prevalence are antibodies against DNA binding histone proteins (H1, H2A/H2B, H3 and H4). They can be found in up to 50 % of all SLE patient sera. Their frequency increases to 80 % in patients with the acute disease. Anti Histone Antibodies (AHA) are of clinical importance for the diagnosis of drug-induced lupus erythematosus. Drugs such as hydralazine, procainamide and isoniazide are known for their LE inducing effect. In addition to antibodies against single histones, antibodies against histone complexes such as H2A-H2B and H3-H4 are frequently found in DIL. Dependent on the inducing drug, up to 90-95 % of DIL patients are positive for histone autoantibodies. However, the test is of limited value as these antibodies are found in other diseases such as infections. AHA have also been found in patients with rheumatoid arthritis, mixed connective tissue disease and progressive scleroderma. The incidence of AHA in these patients however is low ranging from 10 to 15 percent.

In the Varelisa assay the plate is coated with purified human histone proteins H1, H2A, H2B, H3 and H4.

When is the measurement recommended?

Suspicion of drug-induced lupus. 

Antibody isotypes

IgG and IgM (measured with mixed conjugate)

Detection methods

Enzyme-linked immunosorbent assays (ELISA).

References

  • Rubin R. Histone (H2A-H2B)-DNA Autoantibodies. In: Peter JB, Shoenfeld Y (eds) Autoantibodies. 1996; pp 364-372. Elsevier, Amsterdam
  • Harmon CE, Portanova JP. Drug-induced lupus erythematosus. Clin Rheum Dis 1982; 8:121-135
  • Shoenfeld Y, Segol O. Anti-histone antibodies in SLE and other autoimmune diseases. Clin Exp Rheumatol 1989; 7:265-271

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Scl-70 / DNA topoisomerase I

Products

Article No.

No. of tests

Varelisa Scl-70 Antibodies 169 96 96 tests
EliA Scl-70 14-5506-01 2x12 tests

Promotion Material

Performance Folder
EliA ENA (extractable nuclear antigens) (pdf)
Sm, U1RNP, RNP70, Ro, La, Scl-70, CENP, Jo-1 

Antigens

In 1979 antibodies of scleroderma patients where described, which react with a 70 kDa protein. Thus, the antigen was named Scl-70. In 1986, Scl-70 was identified as topoisomerase I (topo-I). Topoisomerase I catalyzes the breaking/rejoining of single-stranded DNA and relaxes supercoiled DNA in vitro. The native enzyme is larger than 70 kDa (100 kDa) but often only its smaller proteolytic fragment is found.

The Varelisa Scl-70 Antibodies assay and the EliA Scl-70 Wells are coated with a human, recombinant Topoisomerase I antigen.

Disease association, antibody prevalence and specificity

  • Scleroderma (30-60%), highly specific 
  • Anti-Scl-70 do not exclude additional AI disorders like SLE, Sjögren's syndrome etc. 
  • Not present in relatives of scleroderma patients or other healthy individuals 
  • Rarely found in Raynaud's syndrome, but than often as predictor of scleroderma

Information about Scleroderma

Anti-Scl-70 are rarely found in the same patients as anti-centromere antibodies.

Disease activity

Most studies found, that titer does not correlate with disease activity or duration. However, there is evidence, that anti-Scl-70 levels correlate with disease severity and activitiy in systemic sclerosis (see reference Hu et al., 2003).

When is the measurement recommended?

Suspicion of scleroderm.

Antibody isotypes

IgG

References

  • Vazquez-Abad D, Rothfield NF (1996) Topoisomerase-I (Scl-70) autoantibodies. In: Peter JB, Shoenfeld Y (eds.), Autoantibodies, pp 830-835, Elsevier Science B.V., Amsterdam 
  • Verheijen R (1996) DNA topoisomerase I. In: Van Venrooij WJ, Maini RN (eds.) Manual of Biological Markers of Disease, Kluwer Academic Publishers, Amsterdam 
  • Spencer-Green G, Alter D, Welch HG (1997) Test performance in systemic sclerosis: Anti-centromere and anti-Scl-70 antibodies. Am J Med 103, 242-248 
  • Hu PQ, Fertig N, Medsger TA, Wright TM (2003) Correlation of Serum Anti-DNA Topoisomerase I Antibody Levels With  Disease Severity and Activity in Systemic Sclerosis. Arthritis Rheum 48, 1363-1373

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Centromere Protein (CENP)

Products

Article No.

No. of tests

Varelisa CENP Antibodies 168 96 96 tests
EliA CENP 14-5505-01 2x12 tests

Promotion Material

Performance Folder
EliA ENA (extractable nuclear antigens) (pdf)
Sm, U1RNP, RNP70, Ro, La, Scl-70, CENP, Jo-1

Antigens

The centromere is the primary constriction site of eukaryotic chromosomes where sister chromatids appear most tightly paired. The three main centromere antigens are CENP-A (19 kDa), CENP-B (80 kDa) and CENP-C (140 kDa) but the most important centromere antigen is the CENP-B. Antibodies to CENP-A and -C are usually cross-reacting and are found almost always in combination with anti-CENP-B antibodies. CENP-B is recognized by virtually all sera with anti-centromere antibodies (ACA).

CENP-B is located within the heterochromatin underneath the kinetochore and probably forms a dimer that binds DNA and has an important role in regulating higher order chromatin structure within the centromere.

The Varelisa CENP Antibodies assay and the EliA CENP Well are coated with human recombinant CENP-B.

Disease association, antibody prevalence and specificity

  • CREST (about 55%)  
  • Raynaud's disease (10-15%)  
  • Diffuse systemic scleroderma (very rarely - ACA in SSc indicate a significantly better prognosis)  
  • Other rheumatic conditions with Raynaud's phenomenon, e.g. rheumatoid arthritis, Sjögren's syndrome etc. (33%)  
  • Primary biliary cirrhosis (PBC) (10-20%) 
  • Not found in healthy individuals, even in low titers (or extremely rare)
ACA are rarely found in the same patients as anti-Scl-70

Disease activity

The titer does not correlate with disease activity or duration.

When is the measurement recommended?

Raynaud's syndrome, suspicion or diagnosis of scleroderma, primary biliary cirrhosis.

Antibody isotype

IgG

References

  • McHugh NJ (1996) Centromere autoantibodies. In: JB Peter, Y Shoenfeld (eds.), Autoantibodies, pp. 161-167, Elsevier Science B.V. 
  • Rothfield NF (1996) Autoantibodies to scleroderma-associated antigens. In: Van Venrooij WJ, Maini RN (eds.), Manual of Biological Markers of Disease, Kluwer Academic Publishers, Amsterdam 
  • Spencer-Green G, Alter D, Welch HG (1997) Test performance in systemic sclerosis: Anti-centromere and anti-Scl-70 antibodies. Am J Med 103, 242-248

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Jo-1 / Histidyl-tRNA-Synthetase 

Products

Article No.

No. of tests

Varelisa Jo-1 Antibodies 167 96 96 tests
Elia Jo-1 14-5507-01 2x12 tests

Promotion Material

Performance Folder
EliA ENA (extractable nuclear antigens) (pdf)
Sm, U1RNP, RNP70, RO, La, Scl-70, CENP, Jo-1

Antigens

Jo-1 is synonymous with histidyl tRNA synthetase. This cytoplasmic enzyme catalyzes the esterification of histidine to its cognate tRNA. Binding of anti-Jo-1 antibodies is localized to the cytoplasm of the various cell types examined. Histidyl tRNA synthetase is persent as a homodimer within the cell; identical subunits of approximately 50 kDa are each bound to tRNA. Anti-Jo-1 sera do not recognize other aminoacyl-tRNA synthetases and only histidyl-tRNA synthetases from higher eukaryotes and react with greatest affinity with human enzyme.

The Varelisa Jo-1 Antibodies assay and the EliA Jo-1 Well are coated with human recombinant Jo-1.

Disease association, antibody prevalence and specificity

  • Adult myositis (about 30%) - almost exclusively in patients with myositis: 54% primary myositis, 40% dermatomyositis, 6% myositis in the setting of another connective tissue disease. Patients with anti-Jo-1 tend to have a severe disease with a tendency to relapse and a poorer prognosis. "Anti-synthetase syndrome" is defined by antibodies to anti-tRNA synthetase.
  • Anti-Jo-1 not in myositis: interstitial lung disease (very rarely)

Disease activity

The antibody usually remains detectable throughout the course of disease, and indefinitely thereafter despite control of disease activity. Occasionally, the antibody becomes undetectable, and in those cases it was assocaited with remission of disease. The clinical utility of anti-Jo-1 antibody fluctuation requires further investigation.

Although it would be extremely unusual for anti-Jo-1 antibodies to develop in a patient who was previously negative for the antibody, repeat testing of such a patient might be considered in order to confirm the accuracy of the previous result in a suggestive clinical situation, such as myositis with interstitial lung disease. In a patient found to be positive, besides confirmatory testing if question exist, repeat testing might be considered as treatment is being discontinued, since the risk of reexacerbation is high if the antibody persists.

When is the measurement recommended?

Suspicion of any kind of myositis.

Antibody isotype

IgG

References

  • Maddison PJ (1996) Aminoacyl-tRNA histidyl (Jo-1) synthetases autoantibodies. In: Peter JB, Shoenfeld Y (eds.), Autoantibodies, pp. 31-35, Elsevier Science B.V, Amsterdam
  • Targoff IN, Plotz PH (1996) The autoantibody system: Anti-aminoacyl-tRNA synthetase antibodies. In: Van Venrooij WJ, Maini RN (eds.), Manual of Biological Markers of Disease, Kluwer Academic Publishers, Amsterdam
  • Delarue M (1995) Aminoacyl-tRNA synthetases. Curr Opini Struct Biol 5, 48-55
  • Targoff IN (1992) Autoantibodies in polymyositis. Rheum Dis Clin North Am 18, 455-482

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