Cytomegalovirus in ulcerative colitis: an evidence-based approach to diagnosis and treatment

Expert Rev Gastroenterol Hepatol. 2022 Feb;16(2):109-120. doi: 10.1080/17474124.2022.2032662. Epub 2022 Jan 31.

Abstract

Introduction: The detection of cytomegalovirus (CMV) in the setting of inflammatory bowel disease often creates confusion whether CMV is a 'bystander' or 'disease.'

Areas covered: This review discusses the clinical conundrum of CMV in ulcerative colitis, approach to discriminate infection from disease, and therapeutic considerations (immunosuppressive and anti-CMV treatment). CMV disease should be considered in corticosteroid refractory- dependent and thiopurine refractory disease. Endoscopy may reveal deep punched out ulcers, irregular ulcers, or cobble-stoning. The diagnosis rests on the presence and abundance of viral inclusion bodies on hematoxylin and eosin stain, positive immunohistochemistry, and/or positive tissue polymerase chain reaction. CMV disease is associated with worse outcomes including increased colectomy rates.

Expert opinion: The timing and duration of antiviral drugs in CMV disease is debatable but depends on the load of CMV in tissue. In high-grade infection, CMV needs to be treated while increasing immunosuppression may work in the setting of low-grade infection. Ganciclovir is the drug of choice for treatment of CMV disease. Tumor necrosis factor inhibitors may be useful for treating underlying disease activity in the setting of CMV. Other emerging therapies include fecal microbiota transplantation. Randomized studies are necessary to define the best timing and duration of anti-CMV therapy.

Keywords: Ulcerative colitis; colectomy; ganciclovir; inflammatory bowel disease; steroids; thiopurine.

Publication types

  • Review

MeSH terms

  • Antiviral Agents / therapeutic use*
  • Colitis, Ulcerative / complications*
  • Colonoscopy
  • Cytomegalovirus Infections / diagnosis*
  • Cytomegalovirus Infections / therapy*
  • Evidence-Based Medicine
  • Fecal Microbiota Transplantation
  • Ganciclovir / therapeutic use
  • Humans
  • Immunohistochemistry
  • Immunosuppressive Agents / therapeutic use*
  • Polymerase Chain Reaction
  • Steroids / therapeutic use
  • Tumor Necrosis Factor-alpha / antagonists & inhibitors

Substances

  • Antiviral Agents
  • Immunosuppressive Agents
  • Steroids
  • Tumor Necrosis Factor-alpha
  • Ganciclovir