ABSTRACT
BACKGROUND: In the pathology of autoimmune hepatitis the immunity mechanism of T-helper 1 (Th1) and Th2 cells was recently evaluated. The purpose of the present study was to measure the mRNA levels in peripheral mononuclear cells and serum cytokines obtained from children with autoimmune hepatitis for a better understanding of the mechanism. METHODS: Twenty-five patients with autoimmune hepatitis and seven controls were enrolled. mRNA levels in peripheral mononuclear cells and serum cytokines were measured using real-time polymerase chain reaction and immunoassay. RESULTS: Serum interferon-gamma (IFN-gamma) and interleukin-4 (IL-4) were rarely detected. In contrast the IFN-gamma/beta-actin mRNA levels were high. CONCLUSION: Autoimmune hepatitis is a Th1-predominant state, therefore immune modulation therapies that target the control of Th1 cytokines should be used.
Subject(s)
Gene Expression , Hepatitis, Autoimmune/genetics , Interferon-gamma/genetics , Interleukin-4/genetics , RNA, Messenger/genetics , Th1 Cells/metabolism , Th2 Cells/metabolism , Actins/biosynthesis , Actins/genetics , Adolescent , Adult , Biomarkers/blood , Child , Child, Preschool , Hepatitis, Autoimmune/blood , Hepatitis, Autoimmune/immunology , Humans , Immunoassay , Interferon-gamma/biosynthesis , Interleukin-4/biosynthesis , Polymerase Chain Reaction , Prognosis , Th1 Cells/immunology , Th2 Cells/immunologyABSTRACT
The cause of influenza to the brain was investigated using the A/NWS/33 influenza virus infected BALB/c mouse model. NOS-2 mRNA levels in the infected mouse brain was greater than in control mice in all brain regions examined, particularly in the olfactory bulb and hippocampus by 1 day p.i. On the contrary, no differences in NOS-1 or NOS-3 mRNA levels were found between infected and control mice. There was also a marked increase in the levels of metabolites of nitric oxide in the olfactory bulb and hippocampus. Immunohistochemistry showed positive staining for anti-NOS-2 primarily in the hippocampus of infected mice. Further, anti-NOS-2 and GFAP staining was mostly found around capillary blood vessels of the hippocampus starting early in the course of the disease. These results indicate that the NWS enhances the activation of astrocytes and NOS-2 expression which in turn enhances NO production and the expansion of capillary blood vessels.
Subject(s)
Brain/metabolism , Glial Fibrillary Acidic Protein/metabolism , Influenza A virus , Nitric Oxide/metabolism , Orthomyxoviridae Infections/metabolism , Animals , Body Weight , Brain/cytology , Glial Fibrillary Acidic Protein/genetics , Male , Mice , Mice, Inbred BALB C , Nitric Oxide Synthase Type II/genetics , Nitric Oxide Synthase Type II/metabolism , Nitric Oxide Synthase Type IIIABSTRACT
To better understand the role of nitric oxide (NO) in pediatric nephrotic syndrome, we measured nitrite/nitrate (NOx) [NO2- and NO3-] in serum obtained from patients with several pediatric kidney diseases and investigated the locations of endothelial nitric oxide synthase (eNOS) and inducible nitric oxide synthase (iNOS). NOx in serum showed significantly higher levels than those in healthy controls (mean +/- SE: 297 +/- 55.7 vs. 158 +/- 13.1 pmol/10 microl). There was no significant difference between six patients with frequent relapse and five patients with nonfrequent relapse. The studies with immunostaining of iNOS and nitrotyrosine were negative for glomerulus in patients with nephrotic syndrome. Those findings suggest that NOx might indirectly influence disease progression in nephrotic syndrome.
Subject(s)
Nephrotic Syndrome/blood , Nitrates/blood , Nitric Oxide Synthase Type III/metabolism , Nitric Oxide Synthase Type II/metabolism , Nitrites/blood , Adolescent , Biomarkers/metabolism , Child , Child, Preschool , Female , Humans , Immunoenzyme Techniques , Infant , Kidney Glomerulus/enzymology , Kidney Glomerulus/pathology , Male , Nephrotic Syndrome/pathology , RecurrenceABSTRACT
We present a rare case of hydranencephaly with cholestasis and giant hepatitis. Studies for infectious agents were all negative including for the detection of virus in liver tissue by using polymerase chain reaction. Although the anterior pituitary functions (cortisol, thyroid stimulating hormone, free T4, human growth hormone) were normal, the patient revealed massive cholestasis and giant hepatitis.
Subject(s)
Cholestasis/pathology , Hepatitis/pathology , Hydranencephaly/pathology , Biomarkers/blood , Biomarkers/urine , Cholestasis/congenital , Cholestasis/diagnosis , Cholestasis/metabolism , Fatal Outcome , Female , Hepatic Insufficiency/congenital , Hepatic Insufficiency/metabolism , Hepatic Insufficiency/pathology , Hepatitis/congenital , Hepatitis/diagnosis , Hepatitis/metabolism , Humans , Hydranencephaly/diagnosis , Hydranencephaly/metabolism , Infant , Tomography, X-Ray Computed , Ultrasonography, InterventionalSubject(s)
Exocrine Pancreatic Insufficiency/genetics , Adolescent , Bone Marrow Diseases/genetics , Bone and Bones/abnormalities , Child , Diabetes Mellitus/etiology , Exocrine Pancreatic Insufficiency/complications , Exocrine Pancreatic Insufficiency/diagnostic imaging , Female , Genes, Recessive , Hepatitis, Chronic/etiology , Humans , Male , Neutropenia/etiology , Radiography , Siblings , SyndromeABSTRACT
The aim of this study was to assess the validity of serum and CSF oxidative status of patients with IE in their initial stage through the d-ROM (Diacron-Reactive Oxygen Metabolites, Italy) test, compared to those with other neurological diseases. The study was conducted on the following four groups: (1) influenza virus-associated encephalopathy (IE, n = 8), including four patients showing neurological sequelae or mortal; (2) influenza virus-associated febrile seizures (IFS, n = 11); (3) febrile convulsion (FC, n = 10): (4) enterovirus-associated encephalopathy (EE, n = 4), including one patient with neurological sequelae. The CSF d-ROM levels in the IE group were significantly higher than those in the IFS and the FC groups but not in the EE group. In addition, general laboratory findings such as leukocytes, platelets, C-reactive protein, aspartate aminotransferase, creatinine, creatinine kinase and LDH, including interleukin-6 (IL-6), were analyzed in each group. The CSF d-ROM levels in the IE group were significantly higher than those in the IFS and FC groups but not in the EE group. As for the serum d-ROM levels and general laboratory findings, with the exception of CSF IL-6 levels in IE, no significant differences were detected compared with the other groups. In patients with IE, the CSF d-ROM levels could be a valid predictive biomarker of the severity, and oxidative stress may be related to the pathogenesis of IE.
