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The status of hematopoietic stem cell transplantation in lysosomal storage disease
Abstract
Lysosomal storage diseases are a group of disorders which have in common an inherited defect in lysosomal function-in most cases, a missing intralysosomal enzyme. Research into potential treatment options for this group of disorders has focused on enzyme replacement. Over the past two decades, hematopoietic stem cell transplantation has been used with increasing frequency to treat patients with lysosomal storage disease by providing a population of cells with the capacity to produce the missing enzyme. The success of marrow transplantation depends on the specific enzyme deficiency and the stage of the disease. Generally, visceral symptoms can be improved, whereas skeletal lesions remain relatively unaffected. The effect on neurologic symptoms varies. Hematopoietic stem cell transplantation remains a viable treatment option in those lysosomal storage diseases where data supportive of disease stabilization or amelioration are known. Early transplantation is the goal so that enzyme replacement may occur before extensive central nervous system injury becomes evident. When inadequate clinical data are available, the decision to perform transplantation requires experimental data demonstrating that the enzyme in question is both excreted from normal cells and taken up by affected cells as evidenced by elimination of storage material in vitro.
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“Hematopoietic cell transplantation following myeloablative conditioning has been used to treat various genetic metabolic syndromes but is largely ineffective in diseases affecting the brain presumably due to poor and variable myeloid cell incorporation into the central nervous system.”
From Treatment of a genetic brain disease by CNS-wide microglia replacement (2022) · cites this paper as [5]
In the citing paper
“In addition to diseases of the bone marrow, allogeneic HCT has been used to treat systemic genetic syndromes (5, 6).”
From Treatment of a genetic brain disease by CNS-wide microglia replacement (2022) · cites this paper as [5]
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Cited by
Treatment of a genetic brain disease by CNS-wide microglia replacement
Shibuya, Y., Kumar, K. K., Mader, M. M.-D., Yoo, Y., Ayala, L. A., Zhou, M., Mohr, M. A., Neumayer, G., Kumar, I., Yamamoto, R., et al. (2022) · Science Translational Medicine · doi:10.1126/scitranslmed.abl9945 · Cited by 126
Enzyme, cell and gene‐based therapies for metachromatic leukodystrophy
Sevin, C., Aubourg, P., & Cartier, N. (2007) · Journal of Inherited Metabolic Disease · doi:10.1007/s10545-007-0540-z · Cited by 88
Metadata
- Authors
- Malatack, J. J., Consolini, D. M., & Bayever, E.
- Venue
- Pediatric Neurology
- Publisher
- Elsevier BV
- Published
- 2003-11
- Volume
- 29
- Issue
- 5
- Pages
- 391-403
- ISSN
- 0887-8994
- Cited by
- 65
- References
- 2
- Language
- en
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- Malatack, J. J., Consolini, D. M., & Bayever, E. (2003). The status of hematopoietic stem cell transplantation in lysosomal storage disease. Pediatric Neurology. https://doi.org/10.1016/j.pediatrneurol.2003.09.003