[Hepatitis C virus-associated cryoglobulinemic vasculitis: A 20-year experience with treatment]

T M Ignatova1, L V Kozlovskaya2, N B Gordovskaya2

  • 1I.M. Sechenov First Moscow State Medical University, Ministry of Health of Russia, Moscow, Russia; V.A. Nasonova Research Institute of Rheumatology, Moscow, Russia.

Insights

Antiviral therapy (AVT) is the preferred treatment for hepatitis C virus (HCV)-associated cryoglobulinemic vasculitis (CV). For severe cases, combining AVT with rituximab offers the best outcomes for patients with HCV-associated CV.

Area of Science:

  • Hepatology
  • Rheumatology
  • Immunology

Background:

  • Hepatitis C virus (HCV)-associated cryoglobulinemic vasculitis (CV) is a serious condition impacting patient prognosis.
  • Understanding treatment efficacy is crucial for managing this complex autoimmune manifestation.

Purpose of the Study:

  • To evaluate the treatment experience of a multidisciplinary hospital for HCV-associated CV.
  • To compare the effectiveness of different therapeutic strategies, including antiviral therapy (AVT) and immunosuppressive therapy (IST).

Main Methods:

  • Retrospective analysis of 72 patients with HCV-associated CV.
  • Assessment of traditional IST (corticosteroids ± cyclophosphamide), rituximab, and AVT.
  • Vasculitis activity measured by Birmingham vasculitis activity score (BVAS); survival and prognostic factors analyzed.

Main Results:

  • Antiviral therapy (AVT) achieved clinical remission in 68% of patients and showed long-term advantages over IST.
  • Rituximab was more effective than traditional IST (73% vs. 13% remission).
  • Combined AVT and rituximab demonstrated highest efficacy in severe CV cases; factors like age >55, liver cirrhosis, and renal failure adversely affected prognosis.

Conclusions:

  • Antiviral therapy (AVT) is the primary treatment for HCV-associated CV.
  • Combination therapy with AVT and rituximab is recommended for severe CV presentations.
  • HCV-associated CV significantly influences the prognosis of chronic HCV infection.
Abstract

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