Is Quantiferon Gold (Interferon Gamma Release Assay) the same as an Interferon Gamma Release Assay (IGRA)?

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QuantiFERON-TB Gold is a Type of Interferon Gamma Release Assay (IGRA)

Yes, QuantiFERON-TB Gold is a specific brand of Interferon Gamma Release Assay (IGRA). QuantiFERON-TB Gold represents one type of IGRA that measures the release of interferon-gamma in blood samples when exposed to specific Mycobacterium tuberculosis antigens 1.

Understanding IGRAs and QuantiFERON-TB Gold

IGRAs are blood tests that detect the release of interferon-gamma (IFN-γ) from sensitized T cells when exposed to specific M. tuberculosis antigens. There are two main types of IGRAs:

  1. QuantiFERON-TB Gold tests - These measure the amount of IFN-γ released using an enzyme-linked immunosorbent assay (ELISA) method 1, 2

    • Original QuantiFERON-TB test (QFT) - now discontinued
    • QuantiFERON-TB Gold (QFT-G)
    • QuantiFERON-TB Gold In-Tube (QFT-GIT)
    • QuantiFERON-TB Gold Plus (QFT-Plus) - the newest version 3
  2. T-SPOT.TB - Uses the ELISPOT method to enumerate cells releasing IFN-γ 2, 4

How QuantiFERON-TB Gold Works

QuantiFERON-TB Gold tests detect the release of interferon-gamma in fresh heparinized whole blood from sensitized persons when incubated with specific M. tuberculosis antigens:

  • Uses synthetic peptides representing M. tuberculosis-specific proteins such as early secretory antigenic target-6 (ESAT-6) and culture filtrate protein-10 (CFP-10) 1, 2
  • These proteins are present in all M. tuberculosis but absent from BCG vaccine strains and most nontuberculous mycobacteria (except M. kansasii, M. szulgai, and M. marinum) 1
  • The newer QFT-Plus has two TB antigen tubes: TB1 (stimulates CD4+ T cells) and TB2 (stimulates both CD4+ and CD8+ T cells) 3

Advantages of IGRAs Over Tuberculin Skin Tests (TST)

  • Results available within 24 hours without requiring a return visit 1, 2
  • Not subject to reader bias or interpretation errors 1, 2
  • Higher specificity in BCG-vaccinated individuals 2
  • Does not trigger an anamnestic response (boosting) 1
  • More specific for M. tuberculosis than tests using purified protein derivative (PPD) 1

Limitations of IGRAs

  • Requires proper blood collection and handling 2
  • May have higher costs than TST (though potentially offset by reduced false positives) 2
  • Cannot distinguish between latent TB infection and active TB disease 2
  • Indeterminate results can occur, particularly in immunocompromised patients 2

Clinical Applications

The CDC recommends that IGRAs like QuantiFERON-TB Gold may be used in all circumstances in which the TST is currently used, including:

  • Contact investigations
  • Evaluation of recent immigrants
  • Sequential-testing surveillance programs for infection control (e.g., healthcare workers) 1

IGRAs are particularly preferred for:

  • BCG-vaccinated individuals
  • Healthcare workers
  • Children under 5 years of age
  • Populations with low rates of return for TST reading 2

Evolution of QuantiFERON Tests

The QuantiFERON tests have evolved over time:

  • Original QFT (approved 2001, now discontinued) - used PPD as antigen 1
  • QFT-G (approved 2005) - uses ESAT-6 and CFP-10 antigens 1
  • QFT-GIT - improved version with antigens in specialized tubes 2
  • QFT-Plus - newest version with additional TB2 tube to capture CD8+ T cell responses 3

Comparative studies show good agreement between newer versions, with QFT-Plus potentially offering advantages for patients with active TB, recent TB, and specific immune conditions involving CD8+ T-cell responses 3.

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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