Test Directory

Test Code
MYO11
Test Name
Myositis Specific 11 Antibody Panel
CPT Codes
84182 X 6, 86235 X 5
Included Tests
  • Jo-1 Ab
  • Pl-7 Ab
  • Pl-12 Ab
  • EJ Ab
  • OJ Ab
  • SRP Ab
  • Mi-2 Alpha Ab
  • Mi-2 Beta Ab
  • MDA5 Ab
  • TIF1 Gamma Ab
  • NXP-2 Ab
Expected Turnaround Time
3 - 5 days
Clinical Utility

Myositis-specific autoantibodies (MSAs) are highly selective, usually exclusive and are associated with particular clinical phenotypes within the myositis spectrum. Myositis-specific autoantibodies to cytoplasmic enzymes that catalyze the binding of specific amino acids to their cognate tRNA define the anti-synthetase syndrome characterized by myositis and lung inflammation, and include autoantibodies to Jo-1 (antihistidyl-tRNA synthetase), PL-7 (threonyl), PL-12 (alanyl), EJ (glycyl), and OJ (isoleucyl).

A further subset of myositis patients is characterized by the presence of autoantibodies directed against the signal recognition particle (SRP). Autoantibodies to Mi-2 (Mi-2/nucleosome remodeling and deacetylase (NuRD) complex) are detected in patients with hallmark dermatomyositis features. Autoantibody to a cytoplasmic 140-kDa protein, melanoma-differentiation associated gene 5 (MDA5), also known as anti-CADM140, identified patients with clinically amyopathic dermatomyositis (CADM) and rapidly progressive lung disease.

Autoantibodies to transcriptional intermediary factor 1-gamma (TIF-1 y), a p155/140 nuclear protein involved in cellular differentiation, have been reported in adult and juvenile dermatomyositis; in adults, it is associated with malignancy. Autoantibodies to nuclear matrix protein NXP-2, another 140-kDa protein, is found in juvenile dermatomyositis (JDM). Anti-TIF-1 y and anti-NXP-2, two novel serological subsets in JDM, occur collectively in >40% of children and appear to identify those with more severe disease.

Specimen and Container Info

Specimen Type: Serum

Preferred Collection Container: Red Top, Plain

Alternate Collection Container: Gold Top, Serum Separator

Desired Specimen Volume: 0.5 mL

Collection Instructions
  1. Collect a red top, plain tube via venipuncture.
Processing and Submission Instructions
  1. Separate serum from cells.
  2. Transfer 0.5 mL of serum to a clear aliquot tube (screw cap).
Patient Preparation

For patients receiving STRENSIQ, consideration should be given to using alternate methods.

Transport Instructions

Transport to the laboratory refrigerated.

Stability Requirements

Room Temperature

 7 days

Refrigerated

 14 days

Frozen

28 days

Methodology
Line Blot
Reference Intervals

See patient report.

Limitations

Administration of STRENSIQ may interfere in certain assays and may falsely elevate values.

Reference Lab
Quest Diagnostics Nichols Institute
Testing Schedule
Routine, 5 times per week