Recommendations for the differential diagnosis of PBC and AIH include:
- Testing for anti-mitochondrial antibodies (AMA)/anti-M2 antibodies and anti-LKM-1 antibodies.1,2
- Confirmatory testing of negative and positive immunofluorescence assay (IFA) results with high-quality solid phase tests to reduce false negative and false positive results.4,5,7
In case of anti-LKM-1 antibodies, the results of IFA and solid phase tests are considered interchangeable.1
Why choose Thermo Fisher Scientific as your partner in autoimmune liver disease diagnostics?
Best-in-class testing to support the diagnosis of PBC
In a scientific study, the EliA™ M2 test demonstrated a comparable sensitivity (100 percent) and a superior specificity (98 percent versus 77 percent) to IFA.8 The EliA M2 test enables you to detect AMA/anti-M2 antibodies with confidence, efficiently.
Best-in-class testing to support the diagnosis of AIH (Type 2)
In a comparative study, the EliA™ LKM-1 test demonstrated a higher sensitivity than IFA (72.8 percent versus 69.1 percent), at the stratified specificity of 94.8 percent, to support the diagnosis of AIH (type 2).9 The EliA LKM-1 test helps clinicians make an accurate diagnosis in this difficult to diagnose disease that can lead to cirrhosis and whose onset usually occurs in childhood and young adulthood.10
Driving efficiency in rare autoimmune disease testing
EliA M2 and EliA LKM-1 tests benefit from the fully automated features on Phadia™ Laboratory Systems. Unlike IFA, laboratorians with standard training can run these tests as part of your Phadia Laboratory Systems workflow. EliA M2 and EliA LKM-1 tests can be performed from the same patient sample at the same time when there is a clinical suspicion of PBC and AIH. For rare tests such as these, the random-access functionality of the Phadia™ 250 instrument and the Phadia™ 2500 series and Phadia™ 5000 series can help streamline workflows, further minimizing the impact on laboratory practice.