Fumagillin Shortage: How to Treat Enterocytozoon bieneusi Microsporidiosis in Solid Organ Transplant Recipients in 2024?

Transpl Int. 2024 Dec 12:37:13518. doi: 10.3389/ti.2024.13518. eCollection 2024.

Abstract

Intestinal microsporidiosis caused by Enterocytozoon bieneusi is an opportunistic infection that especially affects solid organ transplant (SOT) recipients. Management revolves around tapering the immunosuppressive regimen and/or using a specific anti-microsporidia treatment, but only fumagillin has demonstrated efficacy for treatment of this infection. Since fumagillin has been commercially discontinued, nitazoxanide is increasingly being used in this indication. We aimed to describe therapeutic management of E. bieneusi infections in this context. We conducted a French nationwide observational retrospective study on reported cases of E. bieneusi infections in SOT recipients. We identified 154 cases: 64 (41.6%) were managed by simply modifying the immunosuppressive regimen, 54 (35.1%) were given fumagillin, and 36 (23.4%) were given nitazoxanide. Clinical remission rate ranged from 77.8% to 90.7% and was not significantly different between therapeutic strategies but tended to be lower with nitazoxanide. Stool negativization rate was highest with fumagillin (91.7%) and lowest with nitazoxanide (28.6%). Relapses occurred in 6.9% of cases and were more frequent with nitazoxanide (14.3%). This study shows that tapering immunosuppression can result in a satisfactory remission rate but is sometimes accompanied by relapses. Nitazoxanide had limited effectiveness, whereas fumagillin had good results that provide a solid rationale for bringing fumagillin back to market.

Trial registration number: ClinicalTrials.gov ID: NCT05417815.

Keywords: Enterocytozoon bieneusi; infectious diarrhea; microsporidiosis; nitazoxanide; solid organ transplant.

Publication types

  • Observational Study

MeSH terms

  • Adult
  • Aged
  • Antifungal Agents / therapeutic use
  • Cyclohexanes* / therapeutic use
  • Enterocytozoon*
  • Fatty Acids, Unsaturated*
  • Female
  • France
  • Humans
  • Immunosuppressive Agents* / therapeutic use
  • Male
  • Microsporidiosis* / drug therapy
  • Middle Aged
  • Nitro Compounds
  • Opportunistic Infections / drug therapy
  • Organ Transplantation* / adverse effects
  • Retrospective Studies
  • Sesquiterpenes* / therapeutic use
  • Thiazoles / therapeutic use
  • Transplant Recipients

Substances

  • fumagillin
  • Cyclohexanes
  • Fatty Acids, Unsaturated
  • Sesquiterpenes
  • Immunosuppressive Agents
  • nitazoxanide
  • Antifungal Agents
  • Thiazoles
  • Nitro Compounds

Associated data

  • ClinicalTrials.gov/NCT05417815

Grants and funding

The author(s) declare that no financial support was received for the research, authorship, and/or publication of this article.