Evidence map›Paper›PMID 29516328›Full record

ArticleDigestive diseases and sciences2018

Persistence of Circulating Hepatitis C Virus Antigens-Specific Immune Complexes in Patients with Resolved HCV Infection.

Ke-Qin Hu, Wei Cui

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Article in Digestive diseases and sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Ke-Qin HuDivision of GI/Hepatology, University of California, Irvine, School of Medicine, 101 The City Drive, Building 56, Ste. 237, Orange, CA, 92868, USA. kqhu@uci.edu.
Wei CuiDivision of GI/Hepatology, University of California, Irvine, School of Medicine, 101 The City Drive, Building 56, Ste. 237, Orange, CA, 92868, USA.
University of California, Irvine · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOur recent study indicated the possible presence of detectable hepatitis C virus antigens (HCV-Ags) after denaturation of sera with resolved HCV (R-HCV) infection. The present study determined and characterized persistent HCV-Ags-specific immune complexes (ICs) in these patients.

methodsSixty-eight sera with R-HCV and 34 with viremic HCV (V-HCV) infection were tested for free and IC-bound HCV-Ags using HCV-Ags enzyme immunoassay (EIA), the presence of HCV-Ags-specific ICs by immunoprecipitation and Western blot (IP-WB), HCV ICs containing HCV virions using IP and HCV RNA RT-PCR, and correlation of HCV ICs with clinical presentation in these patients.

resultsUsing HCV-Ags EIA, we found 57.4% of sera with R-HCV infection were tested positive for bound, but not free HCV-Ags. Using pooled or individual anti-HCV E1/E2, cAg, NS3, NS4b, and/or NS5a to precipitate HCV-specific-Ags, we confirmed persistent HCV-Ags ICs specific to various HCV structural and non-structural proteins not only in V-HCV infection, but also in R-HCV infection. Using IP and HCV RNA PCR, we then confirmed the presence of HCV virions within circulating ICs in V-HCV, but not in R-HCV sera. Multivariable analysis indicated significant and independent associations of persistent circulating HCV-Ags-specific ICs with both age and the presence of cirrhosis in patients with R-HCV infection.

conclusionsVarious HCV-Ag-specific ICs, but not virions, persist in 57.4% of patients who had spontaneous or treatment-induced HCV clearance for 6 months to 20 years. These findings enriched our knowledge on HCV pathogenesis and support further study on its long-term clinical relevance, such as extrahepatic manifestation, transfusion medicine, and hepatocarcinogenesis.

Indexed as

AdultAgedAged, 80 and overAntigen-Antibody ComplexBiomarkersBlotting, WesternCase-Control StudiesFemaleHepatitis CHepatitis C AntigensHumansImmunoenzyme TechniquesImmunoprecipitationLogistic ModelsMaleMiddle AgedAntigen-Antibody ComplexBiomarkersHepatitis C AntigensHCV core antigen (HCVcAg)HCV immune complexes (HCV ICs)HCV infectionHepatitis C virus antigens (HCV-Ags)Hepatitis C virus (HCV)

Identifiers

PMID29516328
OpenAlexW2794122423

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.