Abstract

ObjectiveTo assess the utility of QuantiFERON®-TB Gold In-tube (QFT-GIT) for targeting preventive therapy in BCG-vaccinated contacts of tuberculosis (TB), based on its high specificity and negative predictive value for development of TB.MethodsWe compared two screening strategies for TB contact tracing in two consecutive periods: the tuberculin skin test (TST) period, when all contacts were screened with the TST alone; and the QFT-GIT period, when BCG-vaccinated contacts underwent TST and QFT-GIT. Diagnosis of TB infection among BCG-vaccinated contacts relied on TST ≥5 mm in the TST period, while in the QFT-GIT period either a positive QFT-GIT or a TST ≥15 mm was required.Measurements and main resultsSix hundred and sixty-one contacts were compared. In the QFT-GIT period there was a reduction in diagnoses of TB infection (77.4% vs. 51.2%; p <0.01) and preventive therapy prescribed (62.1% vs. 48.2%; p = 0.02) among the 290 BCG-vaccinated contacts. After a median follow-up of 5 years, cumulative incidences of TB were 0.62 and 0.29 in the TST and QFT-GIT periods respectively (p = 0.59).ConclusionsIn BCG-vaccinated TB contacts, the addition of QFT-GIT safely reduced TB diagnosis and treatment rates without increasing the risk of subsequent active TB.

Highlights

  • Detection and treatment of recently infected people is an essential measure of tuberculosis (TB) control in low-prevalence countries [1]

  • By contrast to the TST, the interferon-γ release assays (IGRAs), the in vitro immunodiagnostic tests based on M. tuberculosis complex-specific antigens, have no cross-reactivity with the Bacillus Calmette–Guerin (BCG)-vaccine strains and most non-tuberculous mycobacteria [4,5,6]

  • The QuantiFERON®-TB Gold In-tube (QFT-GIT) period included a higher proportion of foreign-born individuals (p

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Summary

Introduction

Detection and treatment of recently infected people is an essential measure of tuberculosis (TB) control in low-prevalence countries [1]. A positive TST response indicates infection with Mycobacterium tuberculosis indirectly, by measuring the delayed-type hypersensitivity response to the intradermal injection of a mixture of wall antigens, the socalled PPD (purified protein-derivate), which is shared by many mycobacteria species and the Bacillus Calmette–Guerin (BCG) strain [2]. By contrast to the TST, the interferon-γ release assays (IGRAs), the in vitro immunodiagnostic tests based on M. tuberculosis complex-specific antigens, have no cross-reactivity with the BCG-vaccine strains and most non-tuberculous mycobacteria [4,5,6]. IGRAs yield fewer positive results than TST, are more specific, and have shown a high negative predictive value for better selecting those immunocompetent individuals who will not develop TB; their use for targeting TB contacts for preventive therapy, especially in BCG-vaccinated subjects, may still be preferable to TST and more cost-effective in certain settings [9]

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