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Age-specific cut-offs for the tuberculin skin test to detect latent tuberculosis in BCG-vaccinated children
Insights
Neonatal bacille Calmette-Guérin (BCG) vaccination wanes in its effect on tuberculin skin test (TST) reactivity by age 6-7 years. New age-specific TST cut-offs are proposed to better detect latent tuberculosis infection (LTBI) in children.
Area of Science:
- Pediatric Infectious Diseases
- Immunology
- Tuberculosis Research
Background:
- Neonatal bacille Calmette-Guérin (BCG) vaccination is widely used globally.
- The tuberculin skin test (TST) is a key tool for diagnosing tuberculosis infection.
- BCG vaccination can affect TST reactivity, complicating the diagnosis of latent tuberculosis infection (LTBI).
Purpose of the Study:
- To evaluate the impact of neonatal BCG vaccination on TST reactivity over time.
- To establish optimal age-specific TST induration cut-off values for detecting LTBI in children.
Main Methods:
- TSTs were administered to 783 children aged 3 months to 14 years with prior neonatal BCG.
- The annual risk of LTBI was estimated using TSTs from 2504 children aged 7 years without BCG scars.
- Goodness-of-fit analysis determined age-specific TST cut-off values.
Main Results:
- BCG's effect on TST induration decreased with age, reaching a minimum at 6-7 years, followed by increased reactivity.
- Optimal age-specific TST cut-off values for LTBI detection were determined: 21 mm (0-1 yr), 18 mm (2-3 yr), 13 mm (4-5 yr), and 10 mm (6-7 yr).
- These new cut-offs showed a strong correlation with the estimated risk of LTBI in the first 7 years (r = 0.93, P < 0.001).
Conclusions:
- The influence of neonatal BCG on TST reactivity diminishes within the first seven years of life.
- Proposed age-specific TST cut-off values can aid in distinguishing BCG response from LTBI in young children.
Objective:
To evaluate the effect of neonatal vaccination with bacille Calmette-Guérin (BCG) on tuberculin skin test (TST) reactivity over time and to define the optimal age-specific induration cut-offs to detect latent tuberculosis infection (LTBI).
Design:
TSTs were performed on 783 children aged 3 months to 14 years who had received neonatal BCG. The estimated annual risk of LTBI was derived from TSTs administered to 2504 children aged 7 years who lacked BCG scars. Goodness-of-fit analysis was used to determine the optimal age-specific cut-off values.
Results:
The effect of neonatal BCG on TST induration waned with age, reaching a nadir at age 6-7 years. This was followed by a rise in TST reactivity. The optimal age-specific TST cut-off values for the detection of LTBI was estimated to be respectively 21, 18, 13 and 10 mm at ages 0-1, 2-3, 4-5 and 6-7 years. There was a close correlation between these new cut-off values with the estimated risk of LTBI for the first 7 years of life (r = 0.93, P < 0.001).
Conclusions:
The effect of neonatal BCG on TST gradually declines over the first 7 years of life. Our proposed new age-specific TST induration cut-off values could help differentiate between response to BCG and LTBI in young children.
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