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. 2025 Jul 23:8830738251353034.
doi: 10.1177/08830738251353034. Online ahead of print.

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

Affiliations

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

Melissa A Wright et al. J Child Neurol. .

Abstract

ObjectivesMore 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.MethodsWe 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November 1, 2024, and surveyed expert clinicians worldwide caring for cerebral adrenoleukodystrophy patients for unpublished agent use.ResultsWe identified 20 publications with primary data on human cerebral adrenoleukodystrophy immunopathology.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 We identified 14 publications reporting use of 7 different agents; unpublished clinician reports identified use of 9 different agents.ConclusionsCerebral adrenoleukodystrophy immunopathology represents complex dysregulation of cytokines,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.

Keywords: ALD; X-linked adrenoleukodystrophy; cerebral ALD; immunopathology; leukodystrophy.

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Conflict of interest statement

Declaration of Conflicting Interest

MAW: has no disclosures.

CDR: has no disclosures

KPVH: Grants from NIH, European Leukodystrophy Association, and the American Academy of Neurology. Participated in clinical trials with bluebird bio, Spur Therapeutics, Minoryx, Ionis. Consulted with Poxel, bluebird bio, and Viking Therapeutics.

TCL: has clinical trials with bluebird bio; consulting for Aspen Therapeutics.

FE: has grants from NIH, the European Leukodystrophy Association and n-Lorem; clinical trials with Minoryx, bluebird bio, ASPA Therapeutics, Calico, and Ionis; consulting with Spur Therapeutics, Affinia Therapeutics, Atlas Venture, Leal Therapeutics, Acadia Pharmaceuticals and Sanofi; writing content for UpToDate.

JLB: has grants from NIH; clinical trials with Spur Therapeutics, Calico, and Ionis; consulting with Ionis; writing content for UpToDate; stock in Orchard Therapeutics; and royalties from BioFire.

Figures

Figure 1.
Figure 1.
PRISMA flow diagram of cALD immunopathology, immunological agent, and biomarker review, showing records identified, included and excluded, and reasons for exclusions.

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