Expanding epidemic of recently acquired HCV in HIV-coinfected patients over a period of 10 years.

Acute HCV infection HCV HIV coinfection MSM NS5B phylogeny

Journal

JHEP reports : innovation in hepatology
ISSN: 2589-5559
Titre abrégé: JHEP Rep
Pays: Netherlands
ID NLM: 101761237

Informations de publication

Date de publication:
Jul 2023
Historique:
received: 04 10 2022
revised: 12 01 2023
accepted: 01 02 2023
medline: 12 6 2023
pubmed: 12 6 2023
entrez: 12 6 2023
Statut: epublish

Résumé

Ongoing transmission of HCV infections is associated with risk factors such as drug injection, needlestick injuries, and men who have sex with men (MSM). Ways of transmission, the course of acute infection, changes of virologic features, and incidence over time are not well known. Over a period of 10 years, n = 161 patients with recently acquired HCV infection (RAHC) (median follow-up 6.8 years) were prospectively enrolled. NS5B sequencing was performed to re-evaluate the HCV genotype (GT) and for phylogenetic analyses. Patients with RAHC were mainly male (92.5%), MSM (90.1%), and HIV-coinfected (86.3%). Transmission risk factors for MSM and non-MSM were sexual risk behaviour (100 and 6.3%, respectively), injection drug use (9.7 and 37.5%, respectively), and nasal drug use (15.2 and 0%, respectively). Spontaneous and interferon- or direct-acting antiviral-based clearance rates were 13.6, 84.3 and 93.4%, respectively. Mean RAHC declined from 19.8 in the first to 13.2 in the past five study years. Although the majority of infections was caused by HCV GT1a, the frequency of HCV GT4d and slightly HCV GT3a increased over time. No relevant clustering of HCV isolates was observed in non-MSM. However, 45% of HCV GT1a and 100% of HCV GT4d MSM cases clustered with MSM isolates from other countries. Travel-associated infections were supported by personal data in an MSM subgroup. No international clustering was detected in MSM with HCV GT1b or HCV GT3a. RAHCs were mainly diagnosed in HIV-coinfected MSM patients and were associated with sexual risk behaviour. Spontaneous clearance rates were low, and phylogenetic clusters were observed in the majority of patients. We evaluated the occurrence and transmission of recently acquired HCV infections (RAHCs) over a period of 10 years. Our data demonstrate that the presence of RAHC was mainly found in HIV-coinfected MSM, with internationally connected transmission networks being observed in the majority of patients. Spontaneous clearance rates were low, and reinfection rates increased mainly driven by a small subset of MSM patients with high-risk behaviour.

Sections du résumé

Background & Aims UNASSIGNED
Ongoing transmission of HCV infections is associated with risk factors such as drug injection, needlestick injuries, and men who have sex with men (MSM). Ways of transmission, the course of acute infection, changes of virologic features, and incidence over time are not well known.
Methods UNASSIGNED
Over a period of 10 years, n = 161 patients with recently acquired HCV infection (RAHC) (median follow-up 6.8 years) were prospectively enrolled. NS5B sequencing was performed to re-evaluate the HCV genotype (GT) and for phylogenetic analyses.
Results UNASSIGNED
Patients with RAHC were mainly male (92.5%), MSM (90.1%), and HIV-coinfected (86.3%). Transmission risk factors for MSM and non-MSM were sexual risk behaviour (100 and 6.3%, respectively), injection drug use (9.7 and 37.5%, respectively), and nasal drug use (15.2 and 0%, respectively). Spontaneous and interferon- or direct-acting antiviral-based clearance rates were 13.6, 84.3 and 93.4%, respectively. Mean RAHC declined from 19.8 in the first to 13.2 in the past five study years. Although the majority of infections was caused by HCV GT1a, the frequency of HCV GT4d and slightly HCV GT3a increased over time. No relevant clustering of HCV isolates was observed in non-MSM. However, 45% of HCV GT1a and 100% of HCV GT4d MSM cases clustered with MSM isolates from other countries. Travel-associated infections were supported by personal data in an MSM subgroup. No international clustering was detected in MSM with HCV GT1b or HCV GT3a.
Conclusions UNASSIGNED
RAHCs were mainly diagnosed in HIV-coinfected MSM patients and were associated with sexual risk behaviour. Spontaneous clearance rates were low, and phylogenetic clusters were observed in the majority of patients.
Impact and Implications UNASSIGNED
We evaluated the occurrence and transmission of recently acquired HCV infections (RAHCs) over a period of 10 years. Our data demonstrate that the presence of RAHC was mainly found in HIV-coinfected MSM, with internationally connected transmission networks being observed in the majority of patients. Spontaneous clearance rates were low, and reinfection rates increased mainly driven by a small subset of MSM patients with high-risk behaviour.

Identifiants

pubmed: 37305441
doi: 10.1016/j.jhepr.2023.100701
pii: S2589-5559(23)00032-0
pmc: PMC10250927
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100701

Informations de copyright

© 2023 The Authors.

Déclaration de conflit d'intérêts

CG has received speaking and/or consulting fees from AbbVie and Gilead. FF has received travel support from Abbvie and Novartis, speaker fees from Abbvie and MSD, and consulting fees from Fresenius and Ibsen. GD has received speaking and/or consulting fees from AbbVie and Gilead. SZ has received speaking and/or consulting fees from Abbvie, BMS, Gilead, Janssen, and Merck/MSD. JD has received research support from Gilead. CZ has received speaking and/or consulting fees from Abbvie, BMS, Gilead, and Merck/MSD, and research support from Abbvie and Gilead. LH, TL, CS, GK, PG, MB, KHP, AM, NW, NF, EH, and NB have no conflicts to disclose. Please refer to the accompanying ICMJE disclosure forms for further details.

Références

J Clin Virol. 2017 Jul;92:42-47
pubmed: 28521213
J Hepatol. 2020 May;72(5):855-864
pubmed: 31862485
AIDS. 2011 Nov 13;25(17):F21-7
pubmed: 21857492
Clin Infect Dis. 2019 Nov 27;69(12):2127-2135
pubmed: 30810158
Can Commun Dis Rep. 2019 Sep 05;45(9):230-237
pubmed: 31650986
AIDS Res Hum Retroviruses. 2015 Jul;31(7):718-22
pubmed: 25858663
Int J Antimicrob Agents. 2019 May;53(5):678-681
pubmed: 30742957
J Infect Dis. 2019 Jun 5;220(1):91-99
pubmed: 30759225
Hepatology. 2014 Nov;60(5):1571-1580
pubmed: 25042607
J Infect Dis. 2004 Jan 15;189(2):292-302
pubmed: 14722895
AIDS. 2013 Oct 23;27(16):2551-7
pubmed: 23736152
Lancet Infect Dis. 2017 Feb;17(2):215-222
pubmed: 28029529
J Viral Hepat. 2014 Jun;21(6):e19-28
pubmed: 24674023
Gut. 2011 Jun;60(6):837-45
pubmed: 21139063
Liver Int. 2018 Jun 30;:
pubmed: 29959866
Clin Infect Dis. 2016 Mar 15;62(6):683-694
pubmed: 26787172
Clin Infect Dis. 2021 Aug 2;73(3):460-467
pubmed: 32459339
Gastroenterology. 2018 Mar;154(4):976-988.e4
pubmed: 29146520
Clin Infect Dis. 2021 Oct 5;73(7):e2194-e2202
pubmed: 32761122
Mol Biol Evol. 2020 May 1;37(5):1530-1534
pubmed: 32011700
J Viral Hepat. 2017 May;24(5):359-370
pubmed: 28027424
Clin Infect Dis. 2013 Aug;57 Suppl 2:S80-9
pubmed: 23884071
Lancet Gastroenterol Hepatol. 2019 Jun;4(6):435-444
pubmed: 30981685
Clin Infect Dis. 2020 Aug 22;71(5):1248-1254
pubmed: 31562816
Liver Int. 2010 Sep;30(8):1169-72
pubmed: 20633101
JAMA Intern Med. 2020 May 1;180(5):637-639
pubmed: 32119030
AIDS. 2017 Jul 17;31(11):1603-1610
pubmed: 28657964
Gastroenterology. 2009 May;136(5):1609-17
pubmed: 19422083
Virology. 2015 Nov;485:213-22
pubmed: 26295281
PLoS One. 2012;7(10):e47335
pubmed: 23110068
Nat Methods. 2017 Jun;14(6):587-589
pubmed: 28481363
Clin Infect Dis. 2021 Jan 27;72(2):233-238
pubmed: 32211763
Clin Infect Dis. 2014 Jan;58(1):136
pubmed: 24046306

Auteurs

Christiana Graf (C)

Department of Internal Medicine 1, University Hospital, Goethe University, Frankfurt, Germany.

Lara Fuhrmann (L)

Department of Biosystems Science and Engineering, ETH Zurich, Basel, Switzerland.
SIB Swiss Institute of Bioinformatics, Basel, Switzerland.

Thomas Lutz (T)

Infektiologikum, Frankfurt, Germany.

Christoph Stephan (C)

HIVCENTER, Department of Infectious Diseases, University Hospital, Goethe University, Frankfurt, Germany.

Gaby Knecht (G)

Infektiologikum, Frankfurt, Germany.

Peter Gute (P)

Infektiologikum, Frankfurt, Germany.

Markus Bickel (M)

Infektiologikum, Frankfurt, Germany.

Kai-Henrik Peiffer (KH)

Department of Internal Medicine 1, University Hospital, Goethe University, Frankfurt, Germany.

Fabian Finkelmeier (F)

Department of Internal Medicine 1, University Hospital, Goethe University, Frankfurt, Germany.

Georg Dultz (G)

Department of Internal Medicine 1, University Hospital, Goethe University, Frankfurt, Germany.

Antonia Mondorf (A)

Department of Internal Medicine 1, University Hospital, Goethe University, Frankfurt, Germany.

Nils Wetzstein (N)

HIVCENTER, Department of Infectious Diseases, University Hospital, Goethe University, Frankfurt, Germany.

Natalie Filmann (N)

Institute of Biostatistics and Mathematical Modeling, Goethe University, Frankfurt, Germany.

Eva Herrmann (E)

Institute of Biostatistics and Mathematical Modeling, Goethe University, Frankfurt, Germany.

Stefan Zeuzem (S)

Department of Internal Medicine 1, University Hospital, Goethe University, Frankfurt, Germany.

Niko Beerenwinkel (N)

Department of Biosystems Science and Engineering, ETH Zurich, Basel, Switzerland.
SIB Swiss Institute of Bioinformatics, Basel, Switzerland.

Julia Dietz (J)

Department of Internal Medicine 1, University Hospital, Goethe University, Frankfurt, Germany.

Christoph Sarrazin (C)

Department of Internal Medicine 1, University Hospital, Goethe University, Frankfurt, Germany.
Medizinische Klinik II, St. Josefs-Hospital, Wiesbaden, Germany.

Classifications MeSH