Variations in IL-22, IL-27 and IL-35 serum levels in untreated and treated hepatitis C patients (notice n° 236175)

détails MARC
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control field 20250112064024.0
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Language code of text/sound track or separate title fre
042 ## - AUTHENTICATION CODE
Authentication code dc
100 10 - MAIN ENTRY--PERSONAL NAME
Personal name Taghinejad, Azam
Relator term author
245 00 - TITLE STATEMENT
Title Variations in IL-22, IL-27 and IL-35 serum levels in untreated and treated hepatitis C patients
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Date of publication, distribution, etc. 2020.<br/>
500 ## - GENERAL NOTE
General note 20
520 ## - SUMMARY, ETC.
Summary, etc. Background: Hepatitis C virus (HCV) is the leading cause of chronic liver diseases including hepatic fibrosis, cirrhosis, and hepatocellular carcinoma. We aimed to assess serum levels of interleukin (IL)-22, IL-27 and IL-35 in patients with hepatitis C and healthy controls to investigate their possible relationship with viral genotypes and liver enzyme levels. Method: A total of 30 newly diagnosed hepatitis C patients with no history of antiviral therapy and 30 healthy individuals participated in this study. Serum levels of IL-22, IL-27 and IL-35 were determined by ELISA in peripheral blood samples from patients prior to and following treament with pan-genotypic direct-acting anti-viral therapy. Serum levels of alanine transaminase (ALT), aspartate transaminase (AST), and alkaline phosphatase (ALP) were measured to determine any possible association between hepatic enzymes and cytokine serum levels concentrations. Result: The results show elevated serum levels of of IL-35 in HCV-infected patients compared to treated cases and healthy controls, whereas there was no significant difference in IL-22 and IL-27 serum levels among the three groups. Additionally, the cytokine levels were not significantly correlated with certain genotypes and levels of liver enzymes. Conclusion: Our findings indicate a potential role for IL-35 in chronic HCV infection and therapeutic management of patients with hepatitis C infection.
690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN)
Topical term or geographic name as entry element sofosbuvir
690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN)
Topical term or geographic name as entry element liver enzymes
690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN)
Topical term or geographic name as entry element daclatasvir
690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN)
Topical term or geographic name as entry element IL-22
690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN)
Topical term or geographic name as entry element IL-35
690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN)
Topical term or geographic name as entry element IL-27
690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN)
Topical term or geographic name as entry element Hepatitis C virus
700 10 - ADDED ENTRY--PERSONAL NAME
Personal name Barani, Shaghik
Relator term author
700 10 - ADDED ENTRY--PERSONAL NAME
Personal name Gholijani, Naser
Relator term author
700 10 - ADDED ENTRY--PERSONAL NAME
Personal name Ghandehari, Farzad
Relator term author
700 10 - ADDED ENTRY--PERSONAL NAME
Personal name Khansalar, Soolmaz
Relator term author
700 10 - ADDED ENTRY--PERSONAL NAME
Personal name Asadipour, Morvarid
Relator term author
700 10 - ADDED ENTRY--PERSONAL NAME
Personal name Davarpanah, Mohammadali
Relator term author
700 10 - ADDED ENTRY--PERSONAL NAME
Personal name Fattahi, Mohammadreza
Relator term author
700 10 - ADDED ENTRY--PERSONAL NAME
Personal name Kalantar, Kurosh
Relator term author
786 0# - DATA SOURCE ENTRY
Note European Cytokine Network | Volume 31 | 4 | 2020-12-01 | p. 134-139 | 1148-5493
856 41 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://shs.cairn.info/revue-european-cytokine-network-2020-4-page-134?lang=en">https://shs.cairn.info/revue-european-cytokine-network-2020-4-page-134?lang=en</a>

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