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Gene expression and promoter region polymorphisms of interleukin-10 in meningitis patients
- Source :
- Genetic testing and molecular biomarkers. 15(5)
- Publication Year :
- 2011
-
Abstract
- Meningitis is an inflammatory disease caused by bacteria, fungi, and viruses with various clinical symptoms. Interleukin-10 (IL-10) levels have been shown to be increased in blood or cerebrospinal fluid of patients with meningitis, but the association of IL-10 gene promoter polymorphisms or gene expression with meningitis has not been evaluated. IL-10 gene promoter polymorphisms A-592C, T-819C, and A-1082G in 61 patients with meningitis and 64 healthy controls were determined by real-time polymerase chain reaction analysis. mRNA from blood and cerebrospinal fluid samples was extracted, and real-time polymerase chain reaction was performed for IL-10 gene expression. No statistically significant differences were found in the allele and genotypic frequencies between patients and control subjects. Expression of IL-10 in meningitis at mRNA levels was detected in the infiltrating leukocytes. IL-10 gene expression in blood from patients was significantly higher than the control group. Our results suggest that there was no association between promoter polymorphisms of IL-10 and meningitis, but a significant increase of IL-10 gene expression was present in patients with meningitis.
- Subjects :
- Adult
Male
Adolescent
Gene Expression
Biology
law.invention
Meningitis, Bacterial
Young Adult
Cerebrospinal fluid
Gene Frequency
law
Gene expression
medicine
Humans
RNA, Messenger
Allele
Child
Promoter Regions, Genetic
Allele frequency
Genetics (clinical)
Polymerase chain reaction
Aged
Polymorphism, Genetic
Infant
Promoter
General Medicine
Middle Aged
medicine.disease
Molecular biology
Meningitis, Viral
Interleukin-10
Interleukin 10
Case-Control Studies
Child, Preschool
Immunology
Female
Meningitis
Subjects
Details
- ISSN :
- 19450257
- Volume :
- 15
- Issue :
- 5
- Database :
- OpenAIRE
- Journal :
- Genetic testing and molecular biomarkers
- Accession number :
- edsair.doi.dedup.....3dfb23e4402167793d1b5a8aba0daa0b