Uncommon immune-mediated extrahepatic manifestations of HCV infection

Ciro Romano1, Giovanna Cuomo1, Roberta Ferrara1

  • 1a Division of Internal Medicine, Department of Medical and Surgical Sciences , "Luigi Vanvitelli" University of Campania , Naples , Italy.

Insights

Chronic hepatitis C virus (HCV) infection can cause many immune-related conditions outside the liver. New direct-acting antiviral agents offer a cure, potentially resolving these HCV-related extrahepatic manifestations.

Area of Science:

  • Hepatology and Immunology
  • Virology
  • Rheumatology

Background:

  • Chronic hepatitis C virus (HCV) infection is linked to diverse extrahepatic manifestations driven by immune dysregulation.
  • Mixed cryoglobulinemia is a well-known immune-mediated complication, but less common manifestations also exist.
  • These include rheumatologic, dermatologic, ophthalmologic, renal, pulmonary, hematologic, cardiovascular, and neuropsychiatric conditions.

Purpose of the Study:

  • To review less common extrahepatic manifestations of HCV infection.
  • To discuss their presumed immune pathogenesis.
  • To evaluate the role of new oral direct-acting antiviral agents (DAAs) in their management.

Main Methods:

  • Literature review of extrahepatic manifestations associated with chronic HCV infection.
  • Analysis of the immunological pathways involved.
  • Assessment of the impact of novel antiviral therapies.

Main Results:

  • HCV-induced immune responses can lead to a wide spectrum of clinical presentations beyond liver disease.
  • Pathogenesis is multifactorial, involving various immune mechanisms.
  • Direct-acting antiviral agents achieve high cure rates for HCV infection.

Conclusions:

  • Etiologic treatment with DAAs is crucial to halt immune-driven hepatic and extrahepatic abnormalities.
  • Cure of HCV infection with modern antiviral therapies is expected to significantly reduce or eliminate these extrahepatic complications.
  • HCV-related extrahepatic manifestations may cease to be a significant comorbidity following successful antiviral treatment.
Abstract

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