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1.
Chinese Medical Journal ; (24): 2225-2230, 2010.
Article in English | WPRIM | ID: wpr-237475

ABSTRACT

<p><b>BACKGROUND</b>The Toll-like receptors (TLRs) represent a group of single-pass transmembrane receptors expressed on sentinel cells that are central to innate immune responses.The aim of this study was to investigate the presence of soluble TLRs in pleural effusions, and the diagnostic values of TLRs for pleural effusion with various etiologies.</p><p><b>METHODS</b>Pleural effusion and serum samples were collected from 102 patients (36 with malignant pleural effusion, 36 with tuberculous pleural effusion, 18 with bacterial pleural effusion, and 12 with transudative pleural effusion). The concentrations of TLR1 to TLR10 were determined in effusion and serum samples by enzyme linked immunosorbent assay. Four classical parameters (protein, lactate dehydrogenase, glucose and C-reactive protein (CRP)) in the pleural fluid were also assessed. Receiver-operating characteristic curves were used to assess the sensitivity and specificity of pleural fluid TLRs and biochemical parameters for differentiating bacterial pleural effusion.</p><p><b>RESULTS</b>The concentrations of TLR1, TLR3, TLR4, TLR7 and TLR9 in bacterial pleural effusion were significantly higher than those in malignant, tuberculous, and transudative groups, respectively. Analysis of receiver operating characteristic curves revealed that the area under the curves of TLR1, TLR3, TLR4, TLR7 and TLR9 were 0.831, 0.843, 0.842, 0.883 and 0.786, respectively, suggesting that these TLRs play a role in the diagnosis of bacterial pleural effusion. Also, the diagnostic value of TLRs for bacterial pleural effusions was much better than that of biochemical parameters (protein, lactate dehydrogenase, glucose and CRP).</p><p><b>CONCLUSIONS</b>The concentrations of TLR1, TLR3, TLR4, TLR7 and TLR9 appeared to be increased in bacterial pleural effusion compared to non-bacterial pleural effusions. Determination of these pleural TLRs may improve the ability of clinicians to differentiate pleural effusion patients of bacterial origin from those with other etiologies.</p>


Subject(s)
Adolescent , Adult , Aged , Aged, 80 and over , Female , Humans , Male , Middle Aged , Young Adult , Bacterial Infections , Metabolism , Enzyme-Linked Immunosorbent Assay , Pleural Effusion , Metabolism , Microbiology , Prospective Studies , Toll-Like Receptor 1 , Metabolism , Toll-Like Receptor 3 , Metabolism , Toll-Like Receptor 4 , Metabolism , Toll-Like Receptor 7 , Metabolism , Toll-Like Receptor 9 , Metabolism , Toll-Like Receptors , Metabolism
2.
Chinese Journal of Medical Genetics ; (6): 306-309, 2006.
Article in Chinese | WPRIM | ID: wpr-263790

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the relationship between the polymorphic (AT)n repeats in 3ountranslated region of exon 4 of CTLA4 gene [CTLA4(AT)n] and Graveso disease (GD) in Zhuang nationality population of Guangxi province.</p><p><b>METHODS</b>The studied groups comprised 48 patients with GD and 44 normal controls. Amplification of target DNA was carried out by polymerase chain reaction (PCR). The amplified products were run by 8% polyacrylamide gel electrophoresis, and then followed by 0.1% silver staining. Some of amplified products were sequenced directly.</p><p><b>RESULTS</b>Nineteen alleles of CTLA4 gene microsatellite polymorphism were found in Guangxi Zhuang nationality individuals. The 106 bp long allele was apparently increased in patients with GD of Zhuang nationality but not in healthy controls (P< 0.05).</p><p><b>CONCLUSION</b>CTLA4 gene microsatellite polymorphism is strongly associated with Graveso disease in Zhuang nationality population of Guangxi province. CTLA4(AT)n 106 bp may be the susceptible gene in GD patients of Zhuang nationality in Guangxi; 19 alleles of CTLA4 gene microsatellite polymorphism were found in Guangxi Zhuang nationality individuals.</p>


Subject(s)
Adult , Female , Humans , Male , Middle Aged , Antigens, CD , Genetics , Base Sequence , CTLA-4 Antigen , China , Dinucleotide Repeats , Genetics , Genetic Predisposition to Disease , Genetics , Graves Disease , Genetics , Molecular Sequence Data , Polymerase Chain Reaction , Polymorphism, Genetic , Genetics , Sequence Analysis, DNA
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