Clinical course and therapeutic approach to varicella zoster virus infection in children with rheumatic autoimmune diseases under immunosuppression

Pediatr Rheumatol Online J. 2016 Jun 2;14(1):34. doi: 10.1186/s12969-016-0095-3.

Abstract

Background: To analyze the clinical presentation and complications of varicella zoster virus (VZV) infection in children with rheumatic diseases treated with immunosuppressive medication such as biological disease-modifying antirheumatic drugs (bDMARDs) and/or conventional disease-modifying antirheumatic drugs (cDMARDs), and to analyze the therapeutic approach to VZV infections with respect to the concomitant immunosuppressive treatment.

Methods: Retrospective multicenter study using the Swiss Pediatric Rheumatology registry. Children with rheumatic diseases followed in a Swiss center for pediatric rheumatology and treated with cDMARD and/or bDMARD with a clinical diagnosis of varicella or herpes zoster between January 2004 and December 2013 were included.

Results: Twenty-two patients were identified, of whom 20 were treated for juvenile idiopathic arthritis, 1 for a polyglandular autoimmune syndrome type III, and 1 for uveitis. Of these 22 patients, 16 had varicella and 6 had herpes zoster. Median age at VZV disease was 7.6 years (range 2 to 17 years), with 6.3 years (range 2 to 17 years) for those with varicella and 11.6 years (range 5 to 16 years) for those with herpes zoster. The median interval between start of immunosuppression and VZV disease was 14.1 months (range 1 to 63 months). Two patients had received varicella vaccine (1 dose each) prior to start of immunosuppression. Concomitant immunosuppressive therapy was methotrexate (MTX) monotherapy (n = 9) or bDMARD monotherapy (n = 2), or a combination of bDMARD with prednisone, MTX or Leflunomide (n = 11). Four patients experienced VZV related complications: cellulitis in 1 patient treated with MTX, and cellulitis, sepsis and cerebellitis in 3 patients treated with biological agents and MTX combination therapy. Six children were admitted to hospital (range of duration: 4 to 9 days) and 12 were treated with valaciclovir or aciclovir.

Conclusion: The clinical course of varicella and herpes zoster in children under immunosuppression is variable, with 4 (18 %) of 22 children showing a complicated course. Thorough assessment of VZV disease and vaccination history and correct VZV vaccination according to national guidelines at diagnosis of a rheumatic autoimmune disease is essential to minimize VZV complications during a later immunosuppressive treatment.

Keywords: Immunosuppression; Pediatric; Rheumatic autoimmune disease; Varicella zoster virus.

Publication types

  • Multicenter Study

MeSH terms

  • Acyclovir / analogs & derivatives
  • Acyclovir / therapeutic use
  • Adolescent
  • Antirheumatic Agents / therapeutic use*
  • Antiviral Agents / therapeutic use
  • Arthritis, Juvenile / complications*
  • Arthritis, Juvenile / drug therapy
  • Chickenpox / complications*
  • Chickenpox / drug therapy
  • Child
  • Child, Preschool
  • Etanercept / therapeutic use
  • Female
  • Herpes Zoster / complications*
  • Herpes Zoster / drug therapy
  • Humans
  • Immunocompromised Host
  • Immunosuppressive Agents / therapeutic use*
  • Isoxazoles / therapeutic use
  • Leflunomide
  • Male
  • Methotrexate / therapeutic use
  • Retrospective Studies
  • Treatment Outcome
  • Valacyclovir
  • Valine / analogs & derivatives
  • Valine / therapeutic use
  • Young Adult

Substances

  • Antirheumatic Agents
  • Antiviral Agents
  • Immunosuppressive Agents
  • Isoxazoles
  • Leflunomide
  • Valine
  • Valacyclovir
  • Etanercept
  • Acyclovir
  • Methotrexate