A safety study on intrathecal delivery of autologous mesenchymal stromal cells in rabbits directly supporting Phase I human trials

Bingkun K. Chen, Nathan P Staff, Andrew M. Knight, Jarred J. Nesbitt, Greg W. Butler, Douglas J. Padley, Joseph E Parisi, Allan B Dietz, Anthony John Windebank

Research output: Contribution to journalArticle

17 Scopus citations

Abstract

Background: There are no effective treatments that slow the progression of neurodegenerative diseases. A major challenge of treatment in neurodegenerative diseases is appropriate delivery of pharmaceuticals into the cerebrospinal fluid (CSF) of affected individuals. Mesenchymal stromal cells (MSCs - either naïve or modified) are a promising therapy in neurodegenerative diseases and may be delivered directly into the CSF where they can reside for months. In this preclinical study, we evaluated the safety of intrathecal autologous MSCs in a rabbit model. Study Design and Methods: Autologous adipose-derived MSCs (or artificial CSF) were delivered intrathecally, either with single or with repeated injections into the foramen magnum of healthy rabbits and monitored for 4 and 12 weeks, respectively. Results: Rabbits tolerated injections well and no definitive MSC-related side effects were observed apart from three rabbits that had delayed death secondary to traumatic foramen magnum puncture. Functional assessments and body weights were equivalent between groups. Gross pathology and histology did not reveal any abnormalities or tumor growth. Complete blood count data were normal and there were no differences in CSF interleukin-6 levels in all groups tested. Conclusion: Our data suggest that intrathecal delivery of autologous MSCs is safe in a rabbit model. Data from this study have supported two successful investigational new drug applications to the Food and Drug Administration, resulting in the initiation of two clinical trials using autologous MSCs in amyotrophic lateral sclerosis and multiple system atrophy.

Original languageEnglish (US)
Pages (from-to)1013-1020
Number of pages8
JournalTransfusion
Volume55
Issue number5
DOIs
StatePublished - May 1 2015

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ASJC Scopus subject areas

  • Hematology
  • Immunology
  • Immunology and Allergy

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