| Literature DB >> 33604556 |
Wenjuan Nie1, Jun Wang1, Wei Jing1, Wenhui Shi1, Qingfeng Wang1, Xuerui Huang1, Baoyun Cai1, Qiping Ge1, Lihui Nie1, Xiqin Han1, Yadong Du1, Jing Wang1, Ru Guo1, Naihui Chu1.
Abstract
Tuberculosis (TB) patient serum cytokine levels may be predictive of anti-tuberculosis treatment progress. Here, serum levels of cytokines TNF-α, IL-4, sIL-2R and IFN-γ were measured then correlated to clinical TB manifestations, bacterial burden, chest imaging findings and clinical course. Study subjects included 67 newly diagnosed pulmonary TB (PTB) patients with active disease admitted to Beijing Chest Hospital for anti-TB chemotherapeutic treatment. Blood was drawn at 0 months (pre-treatment), 1-2 months (at any time between 1 and 2 month) and after 6 months completion of treatment and serum TNF-α, IL-4, sIL-2R and IFN-γ levels were measured in duplicate using enzyme-linked immunosorbent assays (ELISAs). Correlation analysis was conducted to evaluate sensitivity and specificity of cytokine levels as predictors of disease activity and treatment progress. The results indicated that the pre-treatment serum TNF-α level of the smear-negative group was lower than that of the smear 1+ group, while serum TNF-α after 6 months completion of treatment and IFN-γ levels at 1-2 months and after 6 months completion of treatment were significantly lower, respectively, than at 0 months (before treatment) (P < 0.05). Using a cut-off value of 845 pg/ml, serum TNF-α level was predictive of treatment progress, with a sensitivity of 51%, specificity of 60% and AUC of 0.594 (P = 0.013). Meanwhile, using a cut-off value of 393 pg/ml, serum IFN-γ provided superior monitoring efficacy, with a sensitivity of 60%, specificity of 64% and AUC of 0.651 (P = 0.017). In conclusion, both serum TNF-α and IFN-γ levels might be useful biomarkers for monitoring treatment progress.Entities:
Keywords: Biomarker; IFN-γ; IL-4; Serum cytokine; TNF-α; Tuberculosis; sIL-2R
Year: 2020 PMID: 33604556 PMCID: PMC7885884 DOI: 10.1016/j.cytox.2020.100028
Source DB: PubMed Journal: Cytokine X ISSN: 2590-1532