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Compromised function of natural killer cells in acute and chronic viral hepatitis
- Source :
- The Journal of infectious diseases. 209(9)
- Publication Year :
- 2013
-
Abstract
- BACKGROUND Natural killer (NK) cells are an integral part of the innate immune system. They have been suggested to play an important role in both defense against viral hepatitis and the pathogenesis of other liver diseases. METHODS NK cells from 134 individuals including patients with acute hepatitis B and C as well as chronic hepatitis B, C, and delta (D) patients were studied. RESULTS Infection with viral hepatitis was associated with increased frequencies of NK cells in the peripheral blood; that NK cells showed a less activated phenotype and were compromised in cytolotytic function and cytokine production in all viral hepatitis infections: Hepatitis virus infections did not alter NK cell differentiation, and the activity and severity of liver disease were reflected by alterations of NK cell surface receptors as demonstrated by principal component analysis. CONCLUSION NK cell phenotypic and functional alterations can equally be observed in HBV, HCV, and HDV infections. Instead, patterns of NK cell alterations differ in acute and chronic infections. Thus, our data suggest a common mechanism in the alteration of NK cell phenotype and function with unique variations that depend on disease activity rather than virus-specific factors.
- Subjects :
- Adult
Male
Hepatitis C virus
medicine.medical_treatment
Biology
medicine.disease_cause
Pathogenesis
Interleukin 21
Liver disease
Young Adult
Antigens, CD
medicine
Immunology and Allergy
Humans
Aged
Hepatitis, Chronic
Hepatitis B virus
Principal Component Analysis
Innate immune system
Middle Aged
medicine.disease
Virology
Killer Cells, Natural
Infectious Diseases
Cytokine
Phenotype
Case-Control Studies
Immunology
Acute Disease
Female
Viral hepatitis
Subjects
Details
- ISSN :
- 15376613
- Volume :
- 209
- Issue :
- 9
- Database :
- OpenAIRE
- Journal :
- The Journal of infectious diseases
- Accession number :
- edsair.doi.dedup.....5acd6ac6b5d0852a084881fc6bee91cc