Phenotypic and functional alterations of primary human PBMCs induced by HCV non-enveloped capsid-like particles uptake

• Published in: Cellular and molecular life sciences : CMLS Vol. 70; no. 18; pp. 3463 - 3474
• Main Authors: Doumba, Polyxeni P, Serti, Elisavet, Boutsikou, Maria, Konstadoulakis, Manousos M, Georgopoulou, Urania, Koskinas, John
• Format: Journal Article
• Language: English
• Published: Basel Springer-Verlag 01.09.2013; Springer Basel; Springer Nature B.V
• Subjects: Biochemistry; Biomedical and Life Sciences; Biomedicine; blood serum; Capsid - metabolism; CD4-positive T-lymphocytes; CD4-Positive T-Lymphocytes - cytology; CD4-Positive T-Lymphocytes - virology; CD8-positive T-lymphocytes; CD8-Positive T-Lymphocytes - cytology; CD8-Positive T-Lymphocytes - virology; Cell Biology; CTLA-4 Antigen - metabolism; Cytokines; Cytokines - metabolism; Gene Expression Regulation; Genotype & phenotype; Hepacivirus - metabolism; Hepatitis; Hepatitis C virus; Humans; Immune response; interferon-gamma; interleukin-10; Interleukin-10 - metabolism; interleukin-2; Interleukin-2 - metabolism; Interleukin-7 Receptor alpha Subunit - metabolism; Leukocytes, Mononuclear - cytology; Leukocytes, Mononuclear - virology; Life Sciences; messenger RNA; patients; Phenotype; Research Article; secretion; T cell receptors; Time Factors; transcriptional activation; transforming growth factor beta; Transforming Growth Factor beta - metabolism; viral proteins; Cytokines; Hepatitis C virus; Tregs; Non-enveloped particles
• ISSN: 1420-682X; 1420-9071
• DOI: 10.1007/s00018-013-1344-y

Hepatitis C virus non-enveloped particles circulate in the serum of HCV-infected patients and are believed to be involved in viral persistence. It was previously demonstrated that recombinant HCVne particles can efficiently enter T cells. In this study we investigated the effect of this entry on the phenotype and function of PBMCs, focused on the CD4+ and CD8+ T-cells. We have generated recombinant HCVne in the absence of other viral proteins. PBMCs from healthy donors were sampled after incubation either with HCVne or the control at different time points. Levels of expression of CD107a, CD25, CTLA-4, and T regulatory cells were estimated and cytokine expression and secretion were also monitored. Peripheral T cells expressed elevated CD127. The intracellular expression of the inhibitory marker CTLA-4 (CD152) increased significantly on peripheral T cells at late hours post-treatment, compared to the respective non-treated group. Despite the fact that there was an initial immune response due to HCVne uptake, T cells were driven to a partial exhausted phenotype. A significant induction of CD4+CD25+ʰⁱCD127-regulatory T cells at late hours was observed. Consistently, Foxp3+CD4+ T cells were also increased. In parallel, a significant transcriptional activation and increased secretion of IL-2, IL-10, and IFN-γ, was recorded. Moreover, mRNA transcription of TGF-β was considerably elevated. HCVne particles have the potential to shape the immune response by modifying specific phenotypic and functional markers mainly on CD4+ T cells and driving them to partial exhaustion as well as to Treg expansion.