Dawson G, Sun JM, Davlantis KS, Murias M, Franz L, Troy J,
Simmons R, Sabatos-DeVito M, Durham R, Kurtzberg J. Autologous Cord
Blood Infusions Are Safe and Feasible in Young Children with Autism Spectrum
Disorder: Results of a Single-Center Phase I Open-Label Trial. Stem Cells Transl
Med. 2017 May;6(5):1332-1339.
Abstract
Despite advances in early diagnosis and behavioral
therapies, more effective treatments for children with autism spectrum disorder
(ASD) are needed. We hypothesized that umbilical cord blood-derived cell
therapies may have potential in alleviating ASD symptoms by modulating
inflammatory processes in the brain. Accordingly, we conducted a phase I,
open-label trial to assess the safety and feasibility of a single intravenous
infusion of autologous umbilical cord blood, as well as sensitivity to change
in several ASD assessment tools, to determine suitable endpoints for future
trials. Twenty-five children, median age 4.6 years (range 2.26-5.97), with a
confirmed diagnosis of ASD and a qualified banked autologous umbilical cord
blood unit, were enrolled. Children were evaluated with a battery of behavioral
and functional tests immediately prior to cord blood infusion (baseline) and 6
and 12 months later. Assessment of adverse events across the 12-month period
indicated that the treatment was safe and well tolerated. Significant
improvements in children's behavior were observed on parent-report measures of
social communication skills and autism symptoms, clinician ratings of overall
autism symptom severity and degree of improvement, standardized measures of
expressive vocabulary, and objective eye-tracking measures of children's
attention to social stimuli, indicating that these measures may be useful
endpoints in future studies. Behavioral improvements were observed during the
first 6 months after infusion and were greater in children with higher baseline
nonverbal intelligence quotients. These data will serve as the basis for future
studies to determine the efficacy of umbilical cord blood infusions in children
with ASD.
Gesundheit B, Ashwood P, Keating A, Naor D, Melamed M,
Rosenzweig JP. Therapeutic properties of mesenchymal stem cells for autism
spectrum disorders. Med Hypotheses. 2015 Mar;84(3):169-77.
Abstract
Recent studies of autism spectrum disorders (ASD) highlight
hyperactivity of the immune system, irregular neuronal growth and increased
size and number of microglia. Though the small sample size in many of these
studies limits extrapolation to all individuals with ASD, there is mounting
evidence of both immune and nervous system related pathogenesis in at least a
subset of patients with ASD. Given the disturbing rise in incidence rates for
ASD, and the fact that no pharmacological therapy for ASD has been approved by
the Food and Drug Administration (FDA), there is an urgent need for new
therapeutic options. Research in the therapeutic effects of mesenchymal stem
cells (MSC) for other immunological and neurological conditions has shown
promising results in preclinical and even clinical studies. MSC have
demonstrated the ability to suppress the immune system and to promote
neurogenesis with a promising safety profile. The working hypothesis of this
paper is that the potentially synergistic ability of MSC to modulate a
hyperactive immune system and its ability to promote neurogenesis make it an
attractive potential therapeutic option specifically for ASD. Theoretical
mechanisms of action will be suggested, but further research is necessary to
support these hypothetical pathways. The choice of tissue source, type of cell,
and most appropriate ages for therapeutic intervention remain open questions
for further consideration. Concern over poor regulatory control of stem cell
studies or treatment, and the unique ethical challenges that each child with
ASD presents, demands that future research be conducted with particular caution
before widespread use of the proposed therapeutic intervention is implemented.
https://www.cellmedicine.com/stem-cell-therapy-for-autism/
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