Literature DB >> 33818800

miRNA expression profiles in liver grafts of HCV and HIV/HCV-infected recipients, 6 months after liver transplantation.

Michela Bulfoni1, Riccardo Pravisani2, Emiliano Dalla1, Daniela Cesselli1,3, Masaaki Hidaka4, Carla Di Loreto1,3, Susumu Eguchi4, Umberto Baccarani2.   

Abstract

In hepatitis C virus (HCV)/human immunodeficiency virus (HIVco-infected patients, HIV enhances HCV replication and liver damage. Several microRNAs (miRNAs), active in pro-fibrotic and inflammatory pathways, have been implicated in the pathogenesis of this phenomenon. However, these miRNAs have been tested only in explanted cirrhotic livers, when the liver damage has become chronic and irreversible. No data are available on the early phase of viral infection, such as early after liver transplantation (LT). In the present study, the expression of miR-101, miR-122, miR-155, miR-192, miR-200c, miR-338, and miR-532 was determined by quantitative real-time polymerase chain reaction in liver biopsies of HCV (n = 19) and HCV/HIV-infected (n = 20) LT recipients, as well as in a control group (n = 18) of noninfected patients, transplanted for alcoholic cirrhosis. The timing of liver biopsy was 6 months post-LT. None of the patients was treated with direct-acting anti-HCV drugs. All co-infected recipients had suppressed HIV viral load. Grading and staging were assessed according to the Ishak Classification. HCV and HIV viral load were measured in the sera. miR-101 (p = .03), miR-122 (p = .012), and miR-192 (p = .038) were significantly downregulated in HCV/HIV co-infected and HCV mono-infected recipients when compared with noninfected recipients, and such downregulation was more pronounced in co-infected ones. Moreover, in co-infected recipients but not in mono-infected ones, miR-101 inversely correlated with the peripheral HCV-RNA levels (r = .41, p = .04) and miR-122 inversely correlated with peripheral HCV-RNA levels (r = .49, p = .03) and with the histological grading (r = .51, p = .02).  In conclusion, as early as 6 months after LT, the presence of HIV-HCV co-infection enhanced a significant downregulation of certain miRNAs that showed a direct correlation with HCV viral load and liver inflammation.
© 2021 The Authors. Journal of Medical Virology published by Wiley Periodicals LLC.

Entities:  

Keywords:  hepatitis C virus; human immunodeficiency virus; liver transplantation; microRNA; real-time polymerase chain reaction

Year:  2021        PMID: 33818800     DOI: 10.1002/jmv.26999

Source DB:  PubMed          Journal:  J Med Virol        ISSN: 0146-6615            Impact factor:   2.327


  3 in total

Review 1.  Circulating MicroRNAs as a Tool for Diagnosis of Liver Disease Progression in People Living with HIV-1.

Authors:  Miguel Angel Martinez; Cristina Tural; Sandra Franco
Journal:  Viruses       Date:  2022-05-24       Impact factor: 5.818

2.  Reinfection of Transplanted Livers in HCV- and HCV/HIV-Infected Patients Is Characterized by a Different MicroRNA Expression Profile.

Authors:  Emiliano Dalla; Michela Bulfoni; Daniela Cesselli; Riccardo Pravisani; Masaaki Hidaka; Susumu Eguchi; Umberto Baccarani
Journal:  Cells       Date:  2022-02-16       Impact factor: 6.600

Review 3.  The involvement of microRNAs in HCV and HIV infection.

Authors:  Nicky Joshi; Madhuri Chandane Tak; Anupam Mukherjee
Journal:  Ther Adv Vaccines Immunother       Date:  2022-07-05
  3 in total

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