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Jo-1-Ab ELISA

Catalog no.RE75271
Regulatory Status
EU: CE
Kit size
12 x 8
Method
ELISA
Incubation time
3 x 30 min
Standard range
0 - 100 U/mL, cut-off 4 U/mL
Specimen / Volumes
10 µL serum, plasma
Substrate / isotope
TMB 450 nm
instructions for usecertificateMSDS

Enzyme immunoassay for the qualitative and quantitative determination of IgG antibodies against Jo-1 in human serum or plasma (EDTA, citrate or heparin).

Polymyositis (PM) and dermatomyositis (DM) are inflammatory, autoimmune mediated disorders of the connective tissue with unknown etiology (1). They primarily damage skin and/or muscles, but may also affect other organs as e. g. the lung. Without treatment (standard therapy is immune suppression), they tend to develop into a life threatening state(2). Since immunosuppressive agents are known to cause considerable side effects, early diagnosis of PM/DM is essential, in order to keep their dosage as low as possible.

A striking feature of PM/DM is the occurrence of antibodies to aminoacyl-tRNA synthetases; functionally related but immunologically distinct enzymes(3,4,5). About 30 % of all myositis patients carry antibodies against histidyl-tRNA synthetase (EC 6.1.1.21), a 100 kDa dimeric antigen, located in the cytoplasma and known as Jo-1 (derived from a patient’s name) (6). Jo-1 Ab positive sera represent about 75 % of all sera with anti-synthetase autoantibodies (7). With few exceptions, these antibodies tend to be mutually exclusive. (6,8)

The term Jo-1 (or anti-synthetase) syndrome comprises the symptoms of interstitial pulmonary disease with fibrosing alveolitis. For these symptoms, Jo-1 antibodies possess a high predictive value (80 %). In most cases, this condition is clinically significant and may fatally end in adult respiratory distress syndrome (ARDS).(7,9,10)

The present enzyme-linked immuno sorbent assay (ELISA) is intended for the quantitative or qualitative determination of IgG antibodies directed against Jo-1 in human serum or plasma. The antigen used is a highly purified preparation of human histidyl-tRNA synthetase, expressed by baculovirus infected insect cells. The test is fast (incubation time 30 - 30 - 30 minutes) and flexible (divisible solid phase, readyto-use reagents). Six calibrators allow quantitative measurements; a negative and a positive control check the assay performance.

For concrete data please consult the Instruction for Use in the download box on the top right side.

  1. Callen, J. P.: Dermatomyositis: diagnosis, evaluation and management. Minerva Medica 93-3 (2002), 157 - 167
  2. Ghate, J., et al.: A therapeutic update on dermatomyositis/polymyositis. Int J Dermatol 39 (2000), 81 - 87
  3. Mathews, M. B., Bernstein, R. M.: Myositis autoantibody inhibits histidyl-tRNA synthetase: a model for autoimmunity. Nature 304 (1983), 177 - 179
  4. Miller, F. W., et al.: Origin and regulation of a disease-specific antibody response. Antigenic epitopes, spectrotype stability, and isotype restriction of anti-Jo-1 autoantibodies. J Clin Invest 85 (1990), 468 - 475
  5. Miller, F. W., et al.: The role of an autoantigen, histidyl-transfer RNA synthetase, in the induction and maintenance of autoimmunity. Proc Natl Acad Sci USA 87 (1990), 9933 - 9937
  6. Messinger, M.: Autoantikörper bei systemischen entzündlich-rheumatischen Erkrankungen (Kollagenosen). In: L. Thomas (ed.): Labor und Diagnose (2005), TH-Books-Verlags-Gesellschaft, Frankfurt/Main, 1139 - 1161
  7. Thomas, L.: Autoantikörper bei Muskelerkrankungen. In: L. Thomas (ed.): Labor und Diagnose (2005), TH-Books-Verlags-Gesellschaft, Frankfurt/Main, 1161 - 1168
  8. Targoff, I. N.: Myositis antibodies: aminoacyl-tRNA synthetase, signal recognition particle, Mi-2, and PMScl autoantibodies. In: Shoenfield, Y., et al. (eds.): Autoantibodies (2007), Elsevier Science, Amsterdam, 577 - 589
  9. Bernstein, R. M., et al.: Anti-Jo-1 antibody: a marker for myositis with interstitial lung disease. Br Med J 289 (1984), 151 - 152
  10. Sommer, R., Eitelberger, F.: Wertigkeit der Gliadin-Antikörper im Serum zur Diagnose der Zöliakie. Wien Klin Wochenschr 104/4 (1992), 86 - 92

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