| Literature DB >> 35958968 |
Laura Villarreal-Martinez1, Laura Elia MartÍnez-Garza2, Iram Pablo Rodriguez-Sanchez2, Neri Alvarez-Villalobos1, Fernando Guzman-Gallardo1, Sulia Pope-Salazar1, Cynthia Salinas-Silva1, Maria Guadalupe Cepeda-Cepeda1, Alejandra Garza-Bedolla1, Irving Armando Dominguez-Varela1, Daniel Zacarias Villarreal-Martinez1, Jose Humberto Treviño-Villarreal1, David Gomez-Almaguer1.
Abstract
Autism spectrum disorders (ASDs) are a group of neurodevelopmental pathologies characterized by social and communication deficits, for which treatments are limited. Cell therapies, including intrathecal (IT) administration of bone marrow (BM) mononuclear cells (BM-MNC), improves symptoms in patients with ASD. Twenty-four patients diagnosed with ASD, according to the Diagnostic and Statistical Manual of Mental Disorders Text Revision Fourth Edition (DSM-IV-TR) criteria, were autologously treated with IT BM-MNC, and the clinical effect was evaluated using the Childhood Autism Rating Scale (CARS) on Days 30 (n=24) and 180 (n=14) post-treatment. IT BM-MNC improved clinical outcomes by Day 30 (p=0.0039), and those benefits remained and were further accentuated by Day 180 post-treatment (n=14; p=<0.0001). Clinical benefit at Days 30 (p=0.001; r= -0.51) and 180 (p=0.01; r= -0.60) posttreatment positively correlated with the enrichment of a putative BM stem cell population expressing the cluster of differentiation 133+ (CD133+) surface marker.Entities:
Keywords: Asperger’s syndrome; Autism; Rett’s disorder; childhood disintegrate disorder; stem cells
Year: 2022 PMID: 35958968 PMCID: PMC9341312
Source DB: PubMed Journal: Innov Clin Neurosci ISSN: 2158-8333