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Lack of Optimal T-Cell Reactivity Against the Hepatitis C Virus is Associated with the Development of Fibrosis/Cirrhosis During Chronic Hepatitis (from Human Immunology 2003, 64, 224-230)
Bibliografi
Author:
Sreenarasimhaiah, Jayaprakash
;
Jaramillo, Andres
;
Crippin, Jeffrey
;
Lisker-Melman, Mauricio
;
Chapman, William C.
;
Mohanakumar, T.
Topik:
CD4 T cells
;
CD8 T cells
;
Chronic infection
;
Cirrhosis
;
Hepatitis C virus
;
Validation ref - 6
Bahasa:
(EN )
Penerbit:
Elsevier
Tahun Terbit:
2003
Jenis:
Article - diterbitkan di jurnal ilmiah internasional
Fulltext:
sreenarasimhaiah2003.pdf
(129.67KB;
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)
Abstract
Chronic hepatitis C virus (HCV) infection develops in 85% of exposed individuals and 20% develop cirrhosis. However, the pathogenesis of this process is not well-understood. The objective of this study was to determine whether HCV-reactive T cells play a role in the process of development of cirrhosis during chronic HCV infection. We analyzed 21 human leukocyte antigen (HLA)-A2 patients with chronic HCV infection (9 with histology of inflammation and 12 with histology of fibrosis/cirrhosis). The frequency of CD8 T cells reactive to 12 HCV-derived epitopes was determined by an interferon- enzyme-linked immunospot (ELISPOT) assay. The frequency of CD4 Th1 and Th2 cells reactive to the HCV core antigen was determined by interferon- and interleukin-5 ELISPOT assays, respectively. Patients with histology of inflammation showed a significantly higher CD8 T-cell response to five HCV-derived epitopes (YLLPRRGPRL [core], CINGVCWTV [NS3], LLCPAGHAV [NS3], ILAGYGAGV [NS4B], and GLQDCTMLV [NS5B]) as compared with patients with histology of fibrosis/cirrhosis. Also, patients with histology of inflammation showed a significantly higher CD4 Th1 response to the HCV core antigen as compared to patients with histology of fibrosis/cirrhosis. These results indicate that a lack of an optimal T-cell response to HCV is associated with the development of cirrhosis during chronic HCV infection.
[validation ref - 6]
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