HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Diagnostic role of inflammatory and anti-inflammatory cytokines and effector molecules of cytotoxic T lymphocytes in tuberculous pleural effusion.

AbstractBACKGROUND AND OBJECTIVE:
Early diagnosis of tuberculous pleural effusion (TPE) remains difficult. While some inflammatory markers in pleural effusion (PE) are helpful in diagnosis, the roles of anti-inflammatory cytokines and effector molecules of cytotoxic T lymphocytes have not been investigated.
METHODS:
Lymphocyte-predominant exudative PE samples were assayed for inflammatory and anti-inflammatory cytokines and effector molecules of cytotoxic T lymphocytes. Logistic regression analysis was used to predict the probability of TPE and identify independently associated factors. Receiver operating characteristic (ROC) curve analysis was applied to determine the optimal cut-off value for the predicted probability.
RESULTS:
Of 95 patients enrolled, 35 had TPE, 46 had malignant PE and 14 had PE due to other aetiologies. Interferon-γ (IFN-γ), adenosine deaminase (ADA), decoy receptor (DcR) 3, monocyte chemo-attractant protein (MCP)-1, IFN-induced protein (IP)-10, granzyme A and perforin were higher in TPE than in PE of other aetiologies. By logistic regression analysis, IFN-γ ≥ 75 pg/mL, ADA ≥ 40 IU/mL, DcR3 ≥ 9.3 ng/mL and soluble tumour necrosis factor receptor 1 (TNF-sR1) ≥ 3.2 ng/mL were independent factors associated with TPE. The predicted probability based on the four predictors had an area under the ROC curve of 0.920, with 82.9% sensitivity and 86.7% specificity under the cut-off value of 0.303. In the TPE group, patients with positive PE/pleural culture for Mycobacterium tuberculosis had higher pleural IFN-γ, MCP-1, IP-10 and perforin than those with positive sputum but negative PE culture.
CONCLUSIONS:
While pleural interferon-γ and ADA are conventional markers for diagnosing TPE, simultaneous measurements of DcR3 and TNF-sR1 can improve the diagnostic efficacy.
AuthorsChin-Chung Shu, Jann-Yuan Wang, Chia-Lin Hsu, Li-Ta Keng, Kochung Tsui, Jeng-Feng Lin, Hsin-Chih Lai, Chong-Jen Yu, Li-Na Lee, Kwen-Tay Luh
JournalRespirology (Carlton, Vic.) (Respirology) Vol. 20 Issue 1 Pg. 147-54 (Jan 2015) ISSN: 1440-1843 [Electronic] Australia
PMID25355638 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Copyright© 2014 Asian Pacific Society of Respirology.
Chemical References
  • Biomarkers
  • Receptors, Tumor Necrosis Factor, Member 6b
  • Receptors, Tumor Necrosis Factor, Type I
  • Perforin
  • Interferon-gamma
  • Adenosine Deaminase
Topics
  • Adenosine Deaminase (metabolism)
  • Aged
  • Biomarkers (metabolism)
  • Female
  • Humans
  • Inflammation (metabolism, pathology)
  • Interferon-gamma (metabolism)
  • Male
  • Middle Aged
  • Mycobacterium tuberculosis (isolation & purification, pathogenicity)
  • Perforin (metabolism)
  • Pleural Effusion (diagnosis, etiology, metabolism, physiopathology)
  • ROC Curve
  • Receptors, Tumor Necrosis Factor, Member 6b (metabolism)
  • Receptors, Tumor Necrosis Factor, Type I (blood)
  • Sensitivity and Specificity
  • T-Lymphocytes, Cytotoxic (pathology)
  • Tuberculosis, Pleural (complications, diagnosis, metabolism, physiopathology)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: