Serum lymphocytes and cytokines: diagnostic value and influence on the immune status in patients with pulmonary tuberculosis

To determine the absolute number of serum T lymphocytes and cytokine levels and the characteristics of patients with active pulmonary tuberculosis and to assess their effect on the immune status of these patients and their diagnostic and predictive value for tuberculosis. We included 1,069 patients...

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Veröffentlicht in:Jornal brasileiro de pneumologia 2023, Vol.49 (5), p.e20230154-e20230154
Hauptverfasser: Ma, Zhiqiang, Li, Shenghao, Liu, Yuan, Li, Caixin, Wang, Xiaoyan, Tang, Xingrui, Dong, Rui, Zheng, Shitai, Wang, Lin
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Sprache:eng
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Zusammenfassung:To determine the absolute number of serum T lymphocytes and cytokine levels and the characteristics of patients with active pulmonary tuberculosis and to assess their effect on the immune status of these patients and their diagnostic and predictive value for tuberculosis. We included 1,069 patients with active tuberculosis, 51 patients with latent tuberculosis infection, and 600 health individuals. Absolute serum T-lymphocyte counts and cytokine levels were quantified. T lymphocytes were significantly reduced in patients with active tuberculosis when compared with healthy individuals. The immune function of patients gradually decreased with age and was stronger in female patients than in males. Th1 cells expressed higher levels of cytokines than did Th2 cells. Logistic regression analysis showed that reduced CD3+ T, CD8+ T, and NK cell counts, as well as reduced IL-4 and IFN-g expression, were independent influencing factors for active tuberculosis. ROC analysis showed that the sensitivity and specificity of absolute CD3+ T and CD8+ T lymphocyte counts and combined factors were significantly higher than were those of IL-4 and IFN-g for diagnosing active tuberculosis. Serum T-lymphocyte counts and cytokine levels can assess the immune status of tuberculosis patients; they are also useful biomarkers for predicting and diagnosing tuberculosis.
ISSN:1806-3756
1806-3713
1806-3756
DOI:10.36416/1806-3756/e20230154