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The TB GOLD Interferon Gamma Release Assay (IGRA) (NHC) is an advanced blood test used to detect latent tuberculosis infection (LTBI) by measuring the body’s cell-mediated immune response to specific Mycobacterium tuberculosis antigens. Unlike the traditional Tuberculin Skin Test (TST), the IGRA test is not usually affected by prior BCG (Bacillus Calmette-Guérin) vaccination, making it a highly specific method for identifying latent TB infection. A positive result suggests that infection with Mycobacterium tuberculosis is likely, although additional clinical evaluation and diagnostic tests are required to determine whether the infection is latent or active.
This test is commonly recommended for individuals who have been in close contact with TB patients, healthcare workers, people with weakened immune systems, and those at increased risk of tuberculosis. The test requires a blood sample collected in special QuantiFERON-TB Gold tubes or a heparinized blood tube, following specific collection and transport guidelines. No special patient preparation is required. Early detection of latent TB allows healthcare providers to consider preventive treatment, reducing the risk of progression to active tuberculosis and helping control the spread of the disease.
The TB GOLD Interferon Gamma Release Assay (IGRA) (NHC) Test-
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