Literature DB >> 23933510

CD8low T-cell subpopulation is increased in patients with chronic hepatitis B virus infection.

Lichen Ouyang1, Xiaoyi Li, Zhihui Liang, Daofeng Yang, Feili Gong, Guanxin Shen, Xiufang Weng, Xiongwen Wu.   

Abstract

Recent studies suggest that CD8(+) T cells with down-regulated CD8 expression (CD3(+)CD8(low) T cells) represented as a distinct phenotype of CD8(+) T cells are increased and linked to disease severity in some chronically persistent infection, such as chronic HIV and parasite infection. However, the role of CD3(+)CD8(low) T cells in the context of chronic HBV infection is poorly understood. In this study, peripheral blood samples of 47 chronic hepatitis B patients and 19 healthy controls were collected and tested for the frequency and phenotype of CD8(low) T cells. The circulating CD8(low) T cells were significantly more frequent in the patients compared to those in healthy controls, and the CD8(low) T cells in the patients expressed less IFN-γ and more mTGF-β1 than those in the controls, suggesting their type-2 polarized and suppressive properties. Meanwhile, the concentrations of plasma soluble HLA class I molecules were found elevated in the patients, and positively associated with the frequencies of CD8(low) T cells. Furthermore, the CD8(low) T-cell frequency in the HLA-A2-positive patients (n=21) was found negatively correlated with the T-cell responsiveness against the HBc₁₈₋₂₇ peptide, the latter was impaired as revealed by IFN-γ Elispot assay. Our findings suggested that a better understanding of the involvement of CD8(low) T cells in chronically persistent HBV infection would add to our knowledge of the impaired T-cell response in the patients.
Copyright © 2013 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  CD8(low) T subpopulation; Chronic hepatitis B virus infection; HBc(18–27)-specific CD8(+) T-cell response; Membrane-bound TGFβ1

Mesh:

Substances:

Year:  2013        PMID: 23933510     DOI: 10.1016/j.molimm.2013.07.003

Source DB:  PubMed          Journal:  Mol Immunol        ISSN: 0161-5890            Impact factor:   4.407


  7 in total

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  7 in total

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