Kinetics of T-cell-based assays on cerebrospinal fluid and peripheral blood mononuclear cells in patients with tuberculous meningitis

被引:6
|
作者
Park, Ki-Ho [1 ]
Lee, Mi Suk [1 ]
Lee, Sang-Oh [2 ]
Choi, Sang-Ho [2 ]
Kim, Yang Soo [2 ]
Woo, Jun Hee [2 ]
Kang, Joong Koo [3 ]
Lee, Sang-Ahm [3 ]
Kim, Sung-Han [2 ]
机构
[1] Kyung Hee Univ, Sch Med, Dept Internal Med, Div Infect Dis, Seoul, South Korea
[2] Univ Ulsan, Coll Med, Dept Infect Dis, Seoul 138736, South Korea
[3] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Neurol, Seoul 138736, South Korea
来源
KOREAN JOURNAL OF INTERNAL MEDICINE | 2014年 / 29卷 / 06期
基金
新加坡国家研究基金会;
关键词
Tuberculosis; Meningitis; Enzyme-linked immunosorbent assay; Cerebrospinal fluid; INTERFERON-GAMMA RESPONSES; RAPID DIAGNOSIS; RELEASE ASSAYS; ESAT-6; EFFICACY;
D O I
10.3904/kjim.2014.29.6.793
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background/Aims: The goal of this study was to monitor tuberculosis (TB)-specific T-cell responses in cerebrospinal fluid-mononuclear cells (CSF-MCs) and peripheral blood mononuclear cells (PBMCs) in patients with tuberculous meningitis (TBM) over the course of anti-TB therapy. Methods: Adult patients (>= 16 years) with TBM admitted to Asan Medical Center, Seoul, South Korea, were prospectively enrolled between April 2008 and April 2011. Serial brood or CSF samples were collected over the course of the anti-TB therapy, and analyzed using an enzyme-linked immunosorbent spot (ELISPOT) assay. Results: Serial ELISPOT assays were performed on PBMCs from 17 patients (seven definite, four probable, and six possible TBM) and CSF-MC from nine patients (all definite TBM). The median number of interferon-gamma (IFN-gamma)-producing T-cells steadily increased during the first 6 months after commencement of anti-TB therapy in PBMCs. Serial CSF-MC ELISPOT assays revealed significant variability in immune responses during the first 6 weeks of anti-TB therapy, though early increases in CSF-MC ELISPOT results were associated with treatment failure or paradoxical response. Conclusions: Serial analysis of PBMCs by ELISPOT during the course of treatment was ineffective for predicting clinical response. However, increases in TB-specific IFN-gamma-producing T-cells in CSF-MC during the early phase of anti-TB therapy may be predictive of clinical failure.
引用
收藏
页码:793 / 799
页数:7
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