Literature DB >> 31840744

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

Jeffrey M Gelfand1, Ariele L Greenfield1, Matthew Barkovich2, Bryce A Mendelsohn3, Keith Van Haren4, Christopher P Hess1,2, Gabriel N Mannis5.   

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.
© The Author(s) (2019). Published by Oxford University Press on behalf of the Guarantors of Brain. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Entities:  

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

Mesh:

Substances:

Year:  2020        PMID: 31840744     DOI: 10.1093/brain/awz390

Source DB:  PubMed          Journal:  Brain        ISSN: 0006-8950            Impact factor:   13.501


  15 in total

1.  Case Report: Novel CSF1R Variant in a Patient With Behavioral Variant Frontotemporal Dementia Syndrome With Prodromal Repetitive Scratching Behavior.

Authors:  Adit Friedberg; Eliana Marisa Ramos; Zhongan Yang; Luke W Bonham; Jennifer S Yokoyama; Peter A Ljubenkov; Kyan Younes; Daniel H Geschwind; Bruce L Miller
Journal:  Front Neurol       Date:  2022-06-22       Impact factor: 4.086

2.  Dominant-acting CSF1R variants cause microglial depletion and altered astrocytic phenotype in zebrafish and adult-onset leukodystrophy.

Authors:  Woutje M Berdowski; Herma C van der Linde; Marjolein Breur; Nynke Oosterhof; Shanice Beerepoot; Leslie Sanderson; Lieve I Wijnands; Patrick de Jong; Elisa Tsai-Meu-Chong; Walter de Valk; Moniek de Witte; Wilfred F J van IJcken; Jeroen Demmers; Marjo S van der Knaap; Marianna Bugiani; Nicole I Wolf; Tjakko J van Ham
Journal:  Acta Neuropathol       Date:  2022-06-17       Impact factor: 15.887

3.  Altered intrinsic brain activity in patients with CSF1R-related leukoencephalopathy.

Authors:  Jingying Wu; Yikang Cao; Mengting Li; Binyin Li; Xize Jia; Li Cao
Journal:  Brain Imaging Behav       Date:  2022-04-07       Impact factor: 3.224

4.  Is Pre-Symptomatic Immunosuppression Protective in CSF1R-Related Leukoencephalopathy?

Authors:  Philip W Tipton; E Richard Stanley; Violeta Chitu; Zbigniew K Wszolek
Journal:  Mov Disord       Date:  2021-02-15       Impact factor: 10.338

Review 5.  The Role of Microglia in Inherited White-Matter Disorders and Connections to Frontotemporal Dementia.

Authors:  Daniel W Sirkis; Luke W Bonham; Jennifer S Yokoyama
Journal:  Appl Clin Genet       Date:  2021-03-31

Review 6.  Microglial replacement therapy: a potential therapeutic strategy for incurable CSF1R-related leukoencephalopathy.

Authors:  Jinming Han; Heela Sarlus; Zbigniew K Wszolek; Virginija Danylaité Karrenbauer; Robert A Harris
Journal:  Acta Neuropathol Commun       Date:  2020-12-07       Impact factor: 7.801

7.  Attenuated CSF-1R signalling drives cerebrovascular pathology.

Authors:  Conor Delaney; Michael Farrell; Colin P Doherty; Kiva Brennan; Eoin O'Keeffe; Chris Greene; Kieva Byrne; Eoin Kelly; Niamh Birmingham; Paula Hickey; Simon Cronin; Savvas N Savvides; Sarah L Doyle; Matthew Campbell
Journal:  EMBO Mol Med       Date:  2020-12-22       Impact factor: 12.137

8.  Microglial reduction of colony stimulating factor-1 receptor expression is sufficient to confer adult onset leukodystrophy.

Authors:  Fabrizio Biundo; Violeta Chitu; Gabriel G L Shlager; Eun S Park; Maria E Gulinello; Kusumika Saha; Harmony C Ketchum; Christopher Fernandes; Şölen Gökhan; Mark F Mehler; E Richard Stanley
Journal:  Glia       Date:  2020-10-20       Impact factor: 7.452

Review 9.  Modeling CSF-1 receptor deficiency diseases - how close are we?

Authors:  Violeta Chitu; Şölen Gökhan; E Richard Stanley
Journal:  FEBS J       Date:  2021-07-05       Impact factor: 5.622

Review 10.  The multicellular interplay of microglia in health and disease: lessons from leukodystrophy.

Authors:  Woutje M Berdowski; Leslie E Sanderson; Tjakko J van Ham
Journal:  Dis Model Mech       Date:  2021-07-20       Impact factor: 5.758

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