Autoimmunity

Anti-PL-12 Antibodies

Test details

SARDs are a heterogeneous group of disorders characterized by dysregulation of the immune system, that starts to turn against the body’s own tissues. Major SARDs include systemic lupus erythematosus, rheumatoid arthritis, systemic sclerosis and Sjögren’s syndrome. These diseases can affect multiple organs and share common symptoms such as fatigue, fever, joint pain and skin rash. Diagnosis relies on a combination of clinical assessment and specific autoantibody tests. Early diagnosis is crucial to initiate appropriate therapy and slow down disease progression.

 

Anti-PL-7 and anti-PL-12 autoantibodies are directed against tRNA synthetases; specifically, anti-PL-7 targets threonyl-tRNA synthetase, while anti-PL-12 targets alanyl-tRNA synthetase. Both belong to the family of eight anti-synthetase autoantibodies (ASA). These autoantibodies are linked to anti-synthetase syndrome, a condition characterised by interstitial lung disease (ILD), Raynaud’s phenomenon, “mechanic’s hands,” non-erosive arthritis, fever, and occasionally skin rash. The presence of ASA has generally been associated with a better ILD treatment response compared to ILD in myositis patients without ASA. Therefore, their serological detection is highly relevant for identifying different clinical phenotypes, stratifying prognosis and guiding therapeutic management.

Sample type

Serum, EDTA plasma, heparin plasma, citrate plasma

Method

Immunoblot

Preparation

Fasting for at least 8-12 hours before sampling

Storage conditions

Refer to the Health Service Charter to check storage conditions

Shipping

+2/+8°C

References

Betteridge Z, McHugh N. Myositis-specific autoantibodies: an important tool to support diagnosis of myositis. J Intern Med. 2016 Jul;280(1):8-23. doi: 10.1111/joim.12451. Epub 2015 Nov 25. PMID: 26602539.

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