Allogeneic HSCT for adult-onset leukoencephalopathy with spheroids and pigmented glia

Brain. 2020 Feb 1;143(2):503-511. doi: 10.1093/brain/awz390.

Abstract

Adult-onset leukoencephalopathy with spheroids and pigmented glia (ALSP) is an autosomal dominant leukoencephalopathy caused by mutations in colony stimulating factor 1 receptor (CSF1R). Here we report clinical and imaging outcomes following allogeneic haematopoietic stem cell transplantation (HSCT) in two patients with ALSP at the University of California, San Francisco between January 2016 and December 2017. Patient 1 proceeded to transplantation at age 53 with a haplo-identical sibling donor. Patient 2, whose sister and mother had died of the disease, proceeded to transplantation at age 49 with a 12/12 human leukocyte antigen-matched unrelated donor. Both patients received reduced intensity conditioning regimens. At 28 and 26 months post-HSCT, respectively, both patients were alive, without evidence of graft-versus-host disease, with major infection at 1 year in one and new-onset seizures in the other. In both cases, neurological worsening continued post-HSCT; however, the progression in cognitive deficits, overall functional status and gait impairment gradually stabilized. There was continued progression of parkinsonism in both patients. On brain MRI, within 1 year there was stabilization of T2/FLAIR abnormalities, and after 2 years there was complete resolution of abnormal multifocal reduced diffusion. In summary, after >2 years of follow-up, allogeneic HSCT in ALSP led to interval resolution of diffusion MRI abnormalities, stabilization of T2/FLAIR MRI abnormalities, and partial clinical stabilization, supportive of treatment response. Allogeneic HSCT may be beneficial in ALSP by providing a supply of bone marrow-derived brain-engrafting myeloid cells with donor wild-type CSF1R to repopulate the microglial niche.

Keywords: clinical practice; dementia; genetics; leukodystrophy; microglia.

Publication types

  • Case Reports

MeSH terms

  • Brain / physiopathology*
  • Cognition Disorders / pathology
  • Cognition Disorders / physiopathology
  • Disease Progression
  • Female
  • Humans
  • Leukoencephalopathies / genetics*
  • Leukoencephalopathies / therapy
  • Male
  • Microglia / pathology*
  • Middle Aged
  • Mutation / genetics
  • Neuroglia / cytology*
  • Receptors, Granulocyte-Macrophage Colony-Stimulating Factor

Substances

  • Receptors, Granulocyte-Macrophage Colony-Stimulating Factor