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1.
Front Med ; 11(1): 147-151, 2017 Mar.
Article in English | MEDLINE | ID: mdl-27917449

ABSTRACT

Nurses are subjected to high amount of stress in the medical setting, and work-related stress often leads to mental problems. This study aims to investigate the mental health status of nurses exposed to blood through needlestick injuries. A total of 302 nurses working in the hospital of Guangdong, China, participated in this study. Out of the 302 nurses, 140 did not experience any needlestick injuries during the previous week, whereas 162 nurses experienced needlestick injuries. The General Health Questionnaire (GHQ)-28 Standardized Questionnaire, which uses physical, anxiety, social function, and depression subscales, was used in this study. No significant difference between nurses exposed to blood and nurses not exposed to blood was found in terms of gender, age, length of employment, and civil status (P > 0.05). Results from the GHQ-28 Standardized Questionnaire showed that 75.9% (123/162) of nurses exposed to blood were suspected to suffer from mental disorders, whereas 40% (56/140) of nurses not exposed to blood were suspected to suffer from mental disorders. The mean mental health scores of nurses exposed to blood and those not exposed were 8.73 ± 7.32 and 5.69 ± 5.70, respectively. From these results, we can conclude that blood exposure from needlestick injuries leads to higher prevalence of depression, anxiety, and stress symptoms in nurses. This finding highlights the importance of providing efficient, adequate, and appropriate support services after nurses are exposed to blood from needlestick injuries.


Subject(s)
Anxiety/epidemiology , Depression/epidemiology , Needlestick Injuries/epidemiology , Nurses/psychology , Stress, Psychological/epidemiology , Adolescent , Adult , China , Cross-Sectional Studies , Female , Humans , Linear Models , Male , Mental Health , Psychiatric Status Rating Scales , Surveys and Questionnaires , Young Adult
2.
Diagn Microbiol Infect Dis ; 85(2): 154-8, 2016 Jun.
Article in English | MEDLINE | ID: mdl-26680298

ABSTRACT

The dysfunction of peripheral blood mononuclear cell (PBMC) plays an important role in hepatitis B virus (HBV) chronic infection and tolerance. This study is aimed to explore the changes of expression and distribution of Hepatitis B virus core antigen (HBcAg) in the PBMCs of patients infected with chronic hepatitis B virus by using confocal laser scanning microscopy (CLSM). The levels of HBcAg in PBMCs were correlated with the HBV load in serum, and the change of HBcAg distribution in different PBMC organelles may represent various HBV infection states. HBcAg was mainly distributed in the nuclei of PBMC in the cases of immune tolerance and no inflammatory activity. Taken together, our data suggest that the measurement of HBcAg and its distribution in PBMCs using CLSM may serve as an alternative approach to monitor HBV load and the immune states of HBV infection with ease of using and improved sensitivity.


Subject(s)
Blood/virology , Hepatitis B Core Antigens/analysis , Hepatitis B virus/isolation & purification , Hepatitis B, Chronic/virology , Leukocytes, Mononuclear/virology , Viral Load , Adult , Child, Preschool , Female , Humans , Male , Microscopy, Confocal , Middle Aged , Organelles/virology , Young Adult
3.
Article in Chinese | MEDLINE | ID: mdl-23547451

ABSTRACT

OBJECTIVE: To establish the differential expression profiles for exploring new immune mechanism of hepatitis B virus infection. METHODS: DCs were separated from the bone marrow of healthy mouse and cultured in vitro. Then DCs were stimulated with HBsAg, LPS, TNF-alpha, respectively. Twenty-four hours later, the total RNA of cell was extracted. cDNA microarray was used to compare the differential expression of RNA. The significant differential expression of miRNA after the stimulation of HBsAg was chosen. Subsequently, target genes of the significant differential miRNA were forecasted by using computer software. RESULTS: There were 30 miRNAs whose significant differential expressions were beyond two times after the stimulation of HBsAg. Among them, 16 miRNAs expressions were increased and 14 miRNAs expressions were decreased. There was significant difference in differential expression of miRNA among the 3 different stimulations. The selected target genes included relevant elements of signal pathway of DC. CONCLUSION: The alteration of expression profiles of miRNA was specific after DC was stimulated by HBsAg. The selected target genes further demonstrated that miRNA could play important roles in the immune mechanism of HBV infection.


Subject(s)
Dendritic Cells/metabolism , Gene Expression Profiling , Hepatitis B Surface Antigens/pharmacology , MicroRNAs/analysis , Animals , Dendritic Cells/drug effects , Lipopolysaccharides/pharmacology , Male , Mice , Mice, Inbred C57BL , Oligonucleotide Array Sequence Analysis , Tumor Necrosis Factor-alpha/pharmacology
4.
Mol Immunol ; 48(12-13): 1573-7, 2011 Jul.
Article in English | MEDLINE | ID: mdl-21481941

ABSTRACT

HBV replicates noncytopathically in hepatocytes, but HBV or proteins encoded by HBV genome could induce cytokines, chemokines expression by hepatocytes. Moreover, liver damage in patients with HBV infection is immune-mediated and cytokines play important roles in immune-mediated liver damage after HBV infection. Interleukin-32 (IL-32) is a proinflammatory cytokine and plays a critical role in inflammation. However, the role of HBV in IL-32 expression remains unclear. In the present study, we demonstrate that hepatitis B virus protein X (HBx) increases IL-32 expression through the promoter of IL-32 at positions from -746 to +25 and in a dose-dependent manner. Furthermore, we demonstrate that increase of NF-κB subunits p65 and p50 in Huh7 cells also augments IL-32 expression, and the NF-κB inhibitor blocks the effect of HBx on IL-32 induction. These results indicate that NF-κB activation is required for HBx-induced IL-32 expression. In conclusion, IL-32 is induced by HBx in Huh7 cells. Our results suggest that IL-32 might play an important role in inflammatory response after HBV infection.


Subject(s)
Hepatitis B virus/metabolism , Hepatocytes/immunology , Interleukins/genetics , NF-kappa B/metabolism , Trans-Activators/metabolism , Blotting, Western , Cell Line, Tumor , Enzyme-Linked Immunosorbent Assay , Gene Expression Regulation , Hepatitis B/immunology , Hepatocytes/metabolism , Humans , Interleukins/biosynthesis , Interleukins/immunology , Plasmids , Reverse Transcriptase Polymerase Chain Reaction , Signal Transduction , Viral Regulatory and Accessory Proteins
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