Characteristics | TST | IGRA |
---|---|---|
Protocol23,30 | After the 0.1-mL intradermal injection of PPD of Mycobacterium antigens into the patient, the area is measured between 48 to 72 hours for size of induration | After taking a 3- to 5-mL sample of peripheral blood mononuclear cells from the patient, the response of IFN-γ production by T-lymphocytes upon stimulation with specific Mycobacterium tuberculosis antigens (CFP-10, ESAT-6, TB7.7) is measured within 24 hours |
Estimated sensitivity21,32 | 75% to 90% (reduced in immunocompromised patients) | 78% to 92% |
Estimated specificity21,32 | 70% to 95% (reduced in BCG-vaccinated and NTM infections) | 93% to 98% |
Advantages23,33 | No laboratory procedures or costs | May be more cost-effective |
Requires one visit | ||
Objectivity in test interpretation | ||
Disadvantages32 | Requires follow-up visit (48 to 72 hours later) | Requires laboratory procedures |
High subjectivity in test interpretation | Should not be used in children <2 years of age because of limited data in children between 2 and 4 years of age |
BCG, Bacillus Calmette-Guérin; IFN, interferon; NTM, nontuberculous mycobacteria; PPD, purified protein derivative.