QFT is a simple blood test that used for detection of
mycobecterium tuberculosis, the bacteria which causes
tuberculosis (TB).
SAMPLE COLLECTION TUBE FOR QUANTIFERON TB GOLD
PRINCIPLE OF QUANTIFERON TB GOLD
• After 16 to 24 hour incubation period, the tubes are centrifuged, the
plasma is removed and the amount of IFN-y (IU/ml) measured by
ELISA.
• Nil The baseline interferon gamma level produced by the patient’s
lymphocytes.
• Tb Antigen-Nil (TbAg-Nil) The level of interferon-gamma production
by the patient’s lymphocytes due to stimulation by M. tuberculosis
antigens minus the Nil (i.e., basal) level of interferon-gamma.
• Mitogen-Nil The maximum non-specific stimulated interferongamma
level that may be produced by the patient’s lymphocytes minus the Nil
(i.e., basal) level of interferon-gamma.
PROCEDURE OF QUANTIFERON TB GOLD
A. During sample collection
1. In proper mixing / filling : Reduced lymphocytes activity.
2. Reduced incubation time (less than 16 to 24 hour) : Reduced lymphocytes activity.
B. During test procedure
1. Kit have expired.
2. Incomplete washing of plate.
3. Enzyme substrate solution contaminated.
4. Incorrect plate reader filter used.
QUANTIFERON TB GOLD

QUANTIFERON TB GOLD

  • 1.
    QFT is asimple blood test that used for detection of mycobecterium tuberculosis, the bacteria which causes tuberculosis (TB).
  • 3.
    SAMPLE COLLECTION TUBEFOR QUANTIFERON TB GOLD
  • 8.
    PRINCIPLE OF QUANTIFERONTB GOLD • After 16 to 24 hour incubation period, the tubes are centrifuged, the plasma is removed and the amount of IFN-y (IU/ml) measured by ELISA. • Nil The baseline interferon gamma level produced by the patient’s lymphocytes. • Tb Antigen-Nil (TbAg-Nil) The level of interferon-gamma production by the patient’s lymphocytes due to stimulation by M. tuberculosis antigens minus the Nil (i.e., basal) level of interferon-gamma. • Mitogen-Nil The maximum non-specific stimulated interferongamma level that may be produced by the patient’s lymphocytes minus the Nil (i.e., basal) level of interferon-gamma.
  • 9.
  • 12.
    A. During samplecollection 1. In proper mixing / filling : Reduced lymphocytes activity. 2. Reduced incubation time (less than 16 to 24 hour) : Reduced lymphocytes activity. B. During test procedure 1. Kit have expired. 2. Incomplete washing of plate. 3. Enzyme substrate solution contaminated. 4. Incorrect plate reader filter used.