Second-Phase Hepatitis C Plasma Viral Kinetics Directly Reflects Reduced Intrahepatic Burden of Hepatitis C Virus.
direct acting antivirals
intrahepatic infection
single-cell laser capture microdissection
viral kinetics
hepatitis C virus
Journal
The Journal of infectious diseases
ISSN: 1537-6613
Titre abrégé: J Infect Dis
Pays: United States
ID NLM: 0413675
Informations de publication
Date de publication:
11 08 2023
11 08 2023
Historique:
received:
04
10
2022
accepted:
26
01
2023
pmc-release:
01
02
2024
medline:
14
8
2023
pubmed:
2
2
2023
entrez:
1
2
2023
Statut:
ppublish
Résumé
Mathematical models explain how antivirals control viral infections. Hepatitis C virus (HCV) treatment results in at least 2 phases of decline in viremia. The first phase reflects clearance of rapidly produced virions. The second phase is hypothesized to derive from loss of infected cells but has been challenging to prove. Using single-cell methods, we quantified the number of hepatitis C virus (HCV)-infected hepatocytes in liver biopsies taken before and within 7 days of initiating direct-acting antivirals (DAAs) in a double-blinded randomized controlled trial testing 2 (sofosbuvir-velpatasvir) versus 3 (sofosbuvir-velpatasvir-voxilaprevir) DAAs. We employed thousands of intrahepatic measurements in 10 persons with chronic genotype 1a HCV infection: median proportion of infected hepatocytes declined from 11.3% (range, 1.3%-59%) to 0.6% (range, <0.3%-5.8%), a loss of 75%-95% infected hepatocytes. Plasma viremia correlated with numbers of HCV-infected hepatocytes (r = 0.77; P < .0001). Second-phase plasma dynamics and changes in infected hepatocytes were indistinct (P = .16), demonstrating that second-phase viral dynamics derive from loss of infected cells. DAAs led to a decline in intracellular HCV RNA and interferon-stimulated gene expression (P < .05 for both). We proved that second-phase viral dynamics reflect decay of intrahepatic burden of HCV, partly due to clearance of HCV RNA from hepatocytes. NCT02938013.
Sections du résumé
BACKGROUND
Mathematical models explain how antivirals control viral infections. Hepatitis C virus (HCV) treatment results in at least 2 phases of decline in viremia. The first phase reflects clearance of rapidly produced virions. The second phase is hypothesized to derive from loss of infected cells but has been challenging to prove.
METHODS
Using single-cell methods, we quantified the number of hepatitis C virus (HCV)-infected hepatocytes in liver biopsies taken before and within 7 days of initiating direct-acting antivirals (DAAs) in a double-blinded randomized controlled trial testing 2 (sofosbuvir-velpatasvir) versus 3 (sofosbuvir-velpatasvir-voxilaprevir) DAAs.
RESULTS
We employed thousands of intrahepatic measurements in 10 persons with chronic genotype 1a HCV infection: median proportion of infected hepatocytes declined from 11.3% (range, 1.3%-59%) to 0.6% (range, <0.3%-5.8%), a loss of 75%-95% infected hepatocytes. Plasma viremia correlated with numbers of HCV-infected hepatocytes (r = 0.77; P < .0001). Second-phase plasma dynamics and changes in infected hepatocytes were indistinct (P = .16), demonstrating that second-phase viral dynamics derive from loss of infected cells. DAAs led to a decline in intracellular HCV RNA and interferon-stimulated gene expression (P < .05 for both).
CONCLUSIONS
We proved that second-phase viral dynamics reflect decay of intrahepatic burden of HCV, partly due to clearance of HCV RNA from hepatocytes.
CLINICAL TRIALS REGISTRATION
NCT02938013.
Identifiants
pubmed: 36722133
pii: 7017769
doi: 10.1093/infdis/jiad025
pmc: PMC10420397
doi:
Substances chimiques
Sofosbuvir
WJ6CA3ZU8B
Antiviral Agents
0
velpatasvir
KCU0C7RS7Z
Lactams, Macrocyclic
0
RNA, Viral
0
Banques de données
ClinicalTrials.gov
['NCT02938013']
Types de publication
Randomized Controlled Trial
Journal Article
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
311-320Subventions
Organisme : NIAID NIH HHS
ID : R01 AI116868
Pays : United States
Organisme : NIDA NIH HHS
ID : R01 DA016065
Pays : United States
Informations de copyright
© The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.
Déclaration de conflit d'intérêts
Potential conflict of interest. J. H. U. reports provision of study drugs by Gilead Sciences. M. S. S. reports scientific advisor board and Data and Safety Monitoring Board (DSMB) (COVID-19 related) membership for Gilead Sciences. All other authors report no potential conflicts. All authors have submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. Conflicts that the editors consider relevant to the content of the manuscript have been disclosed.
Références
Ann Intern Med. 2015 Dec 1;163(11):818-26
pubmed: 26551051
Proc Natl Acad Sci U S A. 2008 May 13;105(19):7034-9
pubmed: 18467494
Gastroenterology. 2016 Dec;151(6):1131-1140.e5
pubmed: 27565882
Gastroenterology. 2017 Jul;153(1):113-122
pubmed: 28390869
Gastroenterology. 2013 Dec;145(6):1404-13.e1-10
pubmed: 23973767
Lancet. 1999 Nov 20;354(9192):1782-5
pubmed: 10577640
Hepatology. 2010 Apr;51(4):1127-36
pubmed: 20044805
Lancet Gastroenterol Hepatol. 2018 Mar;3(3):172-180
pubmed: 29371017
J Viral Hepat. 2020 Mar;27(3):261-269
pubmed: 31670859
Ann Intern Med. 2017 Jun 06;166(11):792-798
pubmed: 28437794
J Viral Hepat. 2021 Feb;28(2):334-344
pubmed: 33128322
Proc Natl Acad Sci U S A. 2005 Feb 22;102(8):2992-7
pubmed: 15710891
N Engl J Med. 2014 May 15;370(20):1879-88
pubmed: 24720702
Lancet Gastroenterol Hepatol. 2016 Oct;1(2):97-104
pubmed: 27917405
AIDS. 2022 Mar 1;36(3):337-346
pubmed: 34690280
Ann Intern Med. 2015 Dec 15;163(12):899-907
pubmed: 26595450
Cold Spring Harb Perspect Med. 2020 Nov 2;10(11):
pubmed: 31964653
Hepatology. 1994 Jul;20(1):15-20
pubmed: 8020885
Lancet. 2015 Mar 21;385(9973):1107-13
pubmed: 25591505
Nat Rev Immunol. 2002 Jan;2(1):28-36
pubmed: 11905835
J Clin Invest. 2020 Jun 1;130(6):3205-3220
pubmed: 32163375
J Infect Dis. 2020 Jul 23;222(4):601-610
pubmed: 32201883
Nature. 2005 Oct 20;437(7062):1167-72
pubmed: 16177806
PLoS Comput Biol. 2014 Nov 13;10(11):e1003934
pubmed: 25393308