U1 RNP Ab in serum

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Etiology

Reference interval

Principle

Highly purified SM/RNP antigen complex is purified from calf thymus, bound to microwells & stabilized for extended shelf life. Diluted patient sera are placed in the microwells & incubated. If anti-RNP (or anti-Sm) antibodies are present, they will bind to the antigen in the microwell. The microwells are then washed to remove residual sample & a second incubation with anti-human IgG conjugated to alkaline phosphatase is carried out. The conjugate will bind immunologically to the anti-SM and/or anti-RNP IgG of the antigen-antibody complex, forming a 'sandwich' consisting of:

Conjugate (Enzyme-labeled Anti-human IgG)

Human anti-SM and/or anti-RNP (IgG)

Well Coated with SM/RNP antigen

Unbound conjugate is removed in the subsequent washing step. Enzyme substrate is then added to the microwell & if bound conjugate is present, the colorless substrate (p-nitrophenyl phosphate), will be hydrolyzed to form a yellow end product, (p-nitrophenol). The reaction is then stopped and the color fixed. The intensity of the color is measured photometrically at 405 nm & is proportional to the concentration of anti-SM and/or anti-RNP present in the patient sample. The anti-Sm antibody value in EU/mL is then subtracted from the test EU/mL to give the anti-RNP value.

Clinical significance

Antibodies to RNP are detected at high frequency (up to 46%) in patients with systemic lupus erythematosus (SLE) either alone or in parallel with Sm antigen. The RNP antigen is very closely associated with the Sm antigen. However, in contrast to anti-Sm, anti-RNP is found in patients with a variety of connective tissue diseases, including scleroderma, rheumatoid arthritis, discoid lupus & Sjogren's syndrome. A very high titer of anti-RNP, in the absence of other antibodies, is highly characteristic of mixed connective tissue disease (MCTD).

SLE patients who produce RNP antibodies in the absence of anti-Sm antibodies have a low frequency of nephritis & antibodies to DNA whereas patients who produce both RNP & Sm have a higher frequency of nephritis & anti-DNA antibodies. The comparative data on anti-Sm & anti-RNP presence/absence & levels can thus have diagnostic significance.

Specimen

Serum is separated from the clot & refrigerated, 2-8 degrees C for short term storage or stored frozen, -20 degrees C, for long term storage. Avoid freeze-thaw cycles. CAUTION: Serum samples should not be heat inactivated, as this may cause false positive results.

Interpretation

More general terms

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Additional terms

References

  1. Henry, John Bernard, Clinical Diagnosis amd Management by Laboratory Methods, W. B. Saunders Co., Philadelphia, 1991. pp 891-892.
  2. The Physicians Guide to Anti-DNA Antibody Testing, Diamedix Corporation, Miami, Aug. 1989. pp 1-6.
  3. Summary of Procedure. DiaMedix Corporation, Miami, June 1991. pp 1-8.
  4. 4.0 4.1 4.2 Medical Knowledge Self Assessment Program (MKSAP) 14, 16, 17 American College of Physicians, Philadelphia 2006, 2012, 2015