^

Health

A
A
A

Antibodies to extracted nuclear antigens in the blood

 
, medical expert
Last reviewed: 23.04.2024
 
Fact-checked
х

All iLive content is medically reviewed or fact checked to ensure as much factual accuracy as possible.

We have strict sourcing guidelines and only link to reputable media sites, academic research institutions and, whenever possible, medically peer reviewed studies. Note that the numbers in parentheses ([1], [2], etc.) are clickable links to these studies.

If you feel that any of our content is inaccurate, out-of-date, or otherwise questionable, please select it and press Ctrl + Enter.

Normally, the concentrations of antibodies to extracted nuclear antigens RNP / Sm, Sm, SS-A (Ro), SS-B (La) - less than 20 IU / ml, 20-25 IU / ml - boundary values; to the antigen Scl-70 antibodies are normally absent.

This study consists in the quantitative determination of IgG-AT against extractable nuclear antigens - RNP / Sm, Sm, SS-A (Ro) and SS-B (La) in serum. Antibodies to extracted nuclear antigens (ENA) are complexes of soluble ribonucleoproteins. Antibodies against various nuclear antigens are an important diagnostic feature for monitoring and diagnosing various rheumatic diseases.

  • Antibodies to RNP / Sm antigens (AT to the protein components of U 1 - small nuclear ribonucleoprotein - U 1 RNA) are detected with mixed connective tissue disease, less often with systemic lupus erythematosus and other rheumatic diseases. The concentration of antibodies does not correlate with the activity and development of exacerbation. In patients with systemic lupus erythematosus, in the serum of which antibodies to Sm-Ar are present, antibodies to the ribonucleoprotein are not detected. To avoid false positive results, an immunoblot analysis is used.
  • Sm-Ar consists of five small nuclear RNAs (U 1, U 2, U 4, U 5, U 6 ) associated with 11 or more polypeptides (A ', B ' / B ', C, D, E, F , G). Antibodies to the Sm antigen are specific for systemic lupus erythematosus and are present in 30-40% of patients with this disease. These antibodies are very rare in other connective tissue diseases (in the latter case, their detection indicates a combination of diseases). The concentration of antibodies to the Sm antigen does not correlate with the activity and clinical subtypes of systemic lupus erythematosus. Antibody to the Sm antigen is one of the criteria for diagnosing systemic lupus erythematosus.

The frequency of detection of antibodies to various extractable nuclear antigens

Type АТ

Diseases

Frequency,%

Sm

Systemic lupus erythematosus

10-40

PNP

Systemic lupus erythematosus

20-30

 

Mixed connective tissue diseases

95-100

SS-A (Ro)

Systemic lupus erythematosus

15-33

 

Systemic scleroderma

60

 

Neonatal lupus erythematosus

100

 

Sjogren's Syndrome

40-70

SS-B (La)

Systemic lupus erythematosus

10-15

 

Systemic scleroderma

25

 

Sjogren's Syndrome

15-60

Scl-70

Systemic scleroderma

20-40

  • SS-A (Ro) - polypeptides forming complexes with Ro RNA (hY1, hY3 and hY5). AT to Arg SS-A (Ro) are most often found in Sjogren's syndrome / disease and systemic lupus erythematosus. In systemic lupus erythematosus, the production of these antibodies is associated with a certain set of clinical manifestations and laboratory disorders: photosensitivity, Sjogren's syndrome, hyperproduction of rheumatoid factor. The presence of these antibodies in the blood of pregnant women increases the risk of developing neonatal lupus-like syndrome in newborns. AT to Arg SS-A (Ro) can be increased in 10% of patients with rheumatoid arthritis.
  • SS-B (La) -Ag - nucleocytoplasmic phosphoprotein complex with Ro small nuclear RNA (Ro hY1-hY5), transcriptor of RNA polymerase III. АТ to Ar SS-B (La) is found in diseases and Sjogren's syndrome (40-94%). In systemic lupus erythematosus, antibodies to SS-B (La) are more often detected at the onset of a disease that develops in the elderly (9-35%) and is associated with a low incidence of nephritis.
  • Scl-70-Ar-topoisomerase I is a protein with a molecular weight of 100,000 and its fragment has a molecular weight of 67,000. The AT to Scl-70 is more often detected in diffuse (40%), less often with limited (20%) form of systemic scleroderma. They are highly specific for this disease (sensitivity 20-55% depending on the analytical method) and are a poor prognostic sign. The presence of Scl-70 antibodies in systemic scleroderma in combination with the carriage of HLA-DR3 / DRw52 genes increases the risk of pulmonary fibrosis 17-fold. The detection of Scl-70 antibodies in the blood in patients with an isolated Raynaud phenomenon indicates a high probability of systemic scleroderma.

trusted-source[1], [2], [3], [4], [5], [6]

Translation Disclaimer: For the convenience of users of the iLive portal this article has been translated into the current language, but has not yet been verified by a native speaker who has the necessary qualifications for this. In this regard, we warn you that the translation of this article may be incorrect, may contain lexical, syntactic and grammatical errors.

You are reporting a typo in the following text:
Simply click the "Send typo report" button to complete the report. You can also include a comment.