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Inflammation and Immunomodulation in Cerebral X-linked Adrenoleukodystrophy: Review of Pathology and Interventions

  • Melissa A. Wright
  • , Courtney Demmitt-Rice
  • , Keith P. Van Haren
  • , Troy C. Lund
  • , Florian Eichler
  • , Joshua L. Bonkowsky

Research output: Contribution to journalArticlepeer-review

Abstract

Objectives: More than half of males with X-linked adrenoleukodystrophy (ALD) develop progressive, inflammatory cerebral demyelination (cerebral adrenoleukodystrophy). Treatment for cerebral adrenoleukodystrophy is limited with no standard therapies for advanced cerebral adrenoleukodystrophy. We reviewed cerebral adrenoleukodystrophy literature and expert opinion, compiling immunopathology, biomarkers, and therapies tested. Methods: We reviewed published literature from January 1, 1970, through November 1, 2024, and surveyed expert clinicians worldwide caring for cerebral adrenoleukodystrophy patients for unpublished agent use. Results: We identified 20 publications with primary data on human cerebral adrenoleukodystrophy immunopathology. Seventeen publications reported cerebral adrenoleukodystrophy biomarkers. We identified 14 publications reporting use of 7 different agents; unpublished clinician reports identified use of 9 different agents. Conclusions: Cerebral adrenoleukodystrophy immunopathology represents complex dysregulation of cytokines, macrophages, T cells, astrocytes, oligodendrocytes, and microglia. Partial responses to cerebral adrenoleukodystrophy were noted with intravenous immunoglobulin, sirolimus, leriglitazone, and mycophenolate. Our findings suggest consideration for a randomized platform trial of immunomodulatory agents for advanced cerebral adrenoleukodystrophy.

Original languageEnglish (US)
Pages (from-to)221-234
Number of pages14
JournalJournal of Child Neurology
Volume41
Issue number2
DOIs
StatePublished - Feb 2026

Bibliographical note

Publisher Copyright:
© The Author(s) 2025

Keywords

  • ALD
  • X-linked adrenoleukodystrophy
  • cerebral ALD
  • immunopathology
  • leukodystrophy

PubMed: MeSH publication types

  • Journal Article
  • Review

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