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1.
Article in Chinese | WPRIM | ID: wpr-316917

ABSTRACT

<p><b>OBJECTIVE</b>This study was designed to explore the incidence rate of occult HBV infection in patients with anti-HBc positive alone and analyze the possible reasons of occult infection.</p><p><b>METHODS</b>Sera of 183 patients carrying anti-HBc alone(A < or = 0.1) were collected and real-time PCR was used to select samples with HBV DNA positive. HBV pre-S/S amplification products were obtained by PCR, and clonal sequencing were then used for these samples with HBV DNA positive.</p><p><b>RESULTS</b>DNA quantitative results of three samples were greater than 10(3) copies/ml in 183 samples, with a fraction of 1.6%. Pre-S/S sequencing results of two samples from these three samples were obtained. Point mutations within "a" determinant with Q129R/P mutations and co-existence of the mutant type and wild type were found in the two samples.</p><p><b>CONCLUSIONS</b>Occult HBV infection existed in samples with anti-HBc alone. Factors contributing to the loss of HBsAg detection by immunoassays include S gene mutations and low levels of circulating antigen which are below the assay limit of detection. Occult HBV infection not only can lead to a false clinical diagnosis, but also can result in hematological pollution due to such occult infection of blood donors.</p>


Subject(s)
Humans , Base Sequence , Blood Donors , DNA, Viral , Genotype , Hepatitis B , Diagnosis , Allergy and Immunology , Hepatitis B Antibodies , Hepatitis B Core Antigens , Hepatitis B Surface Antigens , Genetics , Hepatitis B virus , Genetics , Allergy and Immunology , Polymerase Chain Reaction , Protein Precursors , Genetics
2.
Zhongguo dangdai erke zazhi ; Zhongguo dangdai erke zazhi;(12): 413-416, 2006.
Article in Chinese | WPRIM | ID: wpr-357802

ABSTRACT

<p><b>OBJECTIVE</b>Previous studies have shown that bacillus calmette-guerin (BCG) can deviate TH2 response toward TH1 response, resulting in a suppressive effect on the development of asthma/atopy. This study examined the effect of BCG treatment on regulatory T cells in asthmatic mice to investigate the possible mechanism.</p><p><b>METHODS</b>Kunming mice were sensitized and challenged with ovalbumin (OVA) to establish asthmatic models. Asthmatic mice were injected intradermally with BCG five days before and after sensitization. After 24 hrs of last challenge, bronchoaveolar lavage fluid (BALF) and peripheral blood were collected . The total cells and eosinophils were counted in the BALF. The percentage of CD4(+) CD25(+) in peripheral blood was detected with flow cytometry. Single spleen cell suspension was prepared and cultured in 1640 medium for 48 hrs and then the cytokine IL-10 level in the supernatant was determined using ELISA. The mice which were challenged with normal saline were used as the Normal control group.</p><p><b>RESULTS</b>The number of total cells and eosinophils in BALF in asthmatic mice [(27.27 +/- 5.36) x 10(7)/L and (6.59 +/- 1.32) x 10(7)/L respectively] were more than in the Normal control group [(1.52 +/- 0.36) x 10(7)/L and zero respectively] (P < 0.01). The number of total cells and eosinophils in BALF in asthmatic mice were reduced after BCG treatment [(13.71 +/- 3.17) x 10(7)/L and (1.43 +/- 0.37) x 10(7)/L respectively] (P < 0.01). The percentage of CD4(+) CD25(+) in peripheral blood of asthmatic mice [(11.59 +/- 1.33)%] was noticeably lower than that of the Control group [(13.66 +/- 1.68)%] (P < 0.01), but increased significantly in asthmatic mice after BCG treatment [(14.40 +/- 2.70)%] (P < 0.05). The IL-10 level in spleen cell supernatant in the BCG-treated group (7.79 +/- 1.34 pg/mL) also increased compared with that in the untreated asthmatic mice (5.54 +/- 0.66 pg/mL) (P < 0.01).</p><p><b>CONCLUSIONS</b>BCG can markedly inhibit the airway inflammation in asthmatic mice possibly by promoting the production of regulatory T cells.</p>


Subject(s)
Animals , Male , Mice , Asthma , Allergy and Immunology , Therapeutics , BCG Vaccine , Therapeutic Uses , Bronchoalveolar Lavage Fluid , Cell Biology , Interleukin-10 , Physiology , T-Lymphocytes, Regulatory , Allergy and Immunology , Toll-Like Receptor 2 , Physiology
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