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논문 기본 정보

자료유형
학술저널
저자정보
Sunghyun Kim (Yonsei University) Jang-Eun Cho (Daegu Health College) Hyunjung Kim (Yonsei University) Dongsup Lee (Yonsei University) Bo-young Jeon (Yonsei University) Hyejon Lee (Yonsei University) Sang-Nae Cho (Yonsei University) Young Keun Kim (Yonsei University) Hyeyoung Lee (Yonsei University)
저널정보
대한의생명과학회 대한의생명과학회지 대한의생명과학회지 제19권 제2호
발행연도
2013.6
수록면
90 - 97 (8page)

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The tuberculin skin test (TST) and interferon gamma (IFN-γ) release assay (IGRA) have been widely used for diagnosis of latent tuberculosis infection (LTBI). In order to overcome limitations of current LTBI diagnostic methods, the development of a novel molecular assay which is able to measure the IFN-γ messenger RNA (mRNA) expression level after stimulation with Mycobacterium tuberculosis (MTB) specific antigen was recently developed. The ability of a molecular assay to detect MTB infection was similar to commercial IGRA however, the optimal incubation time for stimulating IFN-γ was not yet established. Therefore, in this study the direct comparisons of MTB Ag stimulation times (4 and 24 hrs) were performed for diagnosis of MTB infection. Data showed that the coincident rate between QFT-GIT IFN-γ ELISA and IFN-γ RT-PCR (4 hrs) was 88.35% and that of QFT-GIT and IFN-γ RT-PCR (24 hrs) was 70.85%. Based on a receiver operating characteristic (ROC) curve, the 4 hrs-MTB specific Ag stimulation time for IFN-γ RT-PCR had the significant P value, 95% CI value, and AUC (P < 0.0001, 95% CI=0.82 to 1.02, and AUC=0.9214) in comparison with 24 hrs-MTB specific Ag stimulation time (P = 0.009, 95% CI=0.06 to 0.94, and AUC=0.7711). These results show that 4-hr was the most optimal MTB Ag stimulation time for performing IFN-γ RT-PCR. Although semi-quantitative RT-PCR had a few analytical limitations, it might be useful as an alternative molecular diagnostic method for detecting MTB infection.

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INTRODUCTION
MATERIALS AND METHODS
RESULTS
DISCUSSION
REFERENCES

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UCI(KEPA) : I410-ECN-0101-2014-500-003262882