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Serum soluble CD40 is associated with liver injury in patients with chronic hepatitis B
- Source :
- Experimental and Therapeutic Medicine
- Publication Year :
- 2015
- Publisher :
- Spandidos Publications, 2015.
-
Abstract
- Soluble cluster of differentiation 40 (sCD40) is proteolytically cleaved from membrane-bound CD40 and binds to CD154, thereby inhibiting CD40-CD154-mediated immune responses. The aim of the present study was to clarify the role of sCD40 in chronic hepatitis B (CHB). The sCD40 levels in sera from 132 patients with CHB and 33 healthy individuals were retrospectively measured. sCD40 concentrations in patients with CHB were higher than those in healthy controls, and sCD40 levels correlated positively with serum levels of the liver dysfunction biomarkers alanine transaminase (ALT) and aspartate transaminase (AST). sCD40 concentrations increased with a rise in the severity of liver necroinflammation and fibrosis. Patients with >75% liver tissue staining positive for hepatitis B virus (HBV) antigen expression showed significantly lower sCD40 levels than those who stained negative for the HBV antigen. The area under the receiver operating characteristic curve of sCD40 was greater than that of ALT and AST; thus, sCD40 levels have a high diagnostic accuracy for detecting severe liver inflammation in patients with CHB, and could serve as an immunological marker of hepatic tissue injury.
- Subjects :
- Hepatitis B virus
Liver injury
Cancer Research
CD40
biology
business.industry
fibrosis
Aspartate transaminase
Articles
General Medicine
medicine.disease_cause
medicine.disease
medicine.anatomical_structure
Immunology and Microbiology (miscellaneous)
Alanine transaminase
Antigen
Fibrosis
Hepatocyte
Immunology
hepatocyte
biology.protein
medicine
immune
necroinflammatory
business
Subjects
Details
- ISSN :
- 17921015 and 17920981
- Volume :
- 9
- Database :
- OpenAIRE
- Journal :
- Experimental and Therapeutic Medicine
- Accession number :
- edsair.doi.dedup.....d951bfaec39b1ea1fd2a6f4436f44135
- Full Text :
- https://doi.org/10.3892/etm.2015.2182