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Dynamic changes of interferon gamma release assay results with latent tuberculosis infection treatment.

医学 潜伏性肺结核 肺结核 干扰素 结核菌素 内科学 γ干扰素 病毒学 免疫学 结核分枝杆菌
作者
Henan Xin,Xuetao Cao,Hao Zhang,J. Liu,Shouguo Pan,Xue Li,L. Guan,F. Shen,Zisen Liu,Dakuan Wang,X. Guan,J. Yan,Hengjing Li,Boxuan Feng,Ming Zhang,Qianting Yang,Qi Jin,Lei Gao
出处
期刊:Clinical Microbiology and Infection [Elsevier BV]
卷期号:26 (11) 被引量:2
标识
DOI:10.1016/j.cmi.2020.02.009
摘要

Abstract Objectives Using QuantiFERON-TB Gold In-Tube (QFT-GIT) for monitoring tuberculosis (TB) and latent TB infection treatment effect is controversial. The present study aimed to evaluate the dynamic changes of interferon gamma (IFN-γ) levels along with latent TB infection treatment via a randomized controlled study. Methods A total of 910 participants treated with 8 weeks of once-weekly rifapentine plus isoniazid (group A), 890 treated with 6 weeks of twice-weekly rifapentine plus isoniazid (group B) and 818 untreated controls (group C) were followed for 2 years to track active TB development. QFT-GIT tests were repeated three times for all groups: before treatment (T0), at completion of treatment (T1) and 3 months after completion of treatment (T2). Results Similar rates of persistent QFT-GIT reversion were observed in groups A (19.0%, 173/910), B (18.5%, 165/890) and C (20.7%, 169/818) (p 0.512). The dynamic changes of IFN-γ levels were not statistically significant among the three groups. In treated participants, individuals with higher baseline IFN-γ levels showed increased TB occurrence (1.0%, 9/896) compared to those with lower baseline levels (0.2%, 2/904) (p 0.037). A similar but statistically insignificant trend was also observed in untreated controls (1.8% (7/400) vs. 0.5% (2/418), p 0.100). When TB cases were matched with non-TB cases on baseline IFN-γ levels, no significant differences were found with respect to the dynamic changes in IFN-γ levels with time, regardless of whether they received treatment. Conclusions QFT-GIT reversion or decreased IFN-γ levels should not be used for monitoring host response to latent TB infection treatment.

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