Villarreal-Martinez Laura, MartÍnez-Garza Laura Elia, Rodriguez-Sanchez Iram Pablo, Alvarez-Villalobos Neri, Guzman-Gallardo Fernando, Pope-Salazar Sulia, Salinas-Silva Cynthia, Cepeda-Cepeda Maria Guadalupe, Garza-Bedolla Alejandra, Dominguez-Varela Irving Armando, Villarreal-Martinez Daniel Zacarias, Treviño-Villarreal Jose Humberto, Gomez-Almaguer David
Drs. L Villarreal-Martinez, Alvarez-Villalobos, Guzman-Gallardo, Pope-Salazar, Salinas-Silva, Cepeda-Cepeda, Garza-Bedolla, Dominguez-Varela, DZ Villarreal-Martinez, Treviño-Villarreal, and Gomez-Almaguer are with Hematology Service, Hospital Universitario "Dr. José Eleuterio González" in Monterrey, Mexico.
Drs. Martínez-Garza and Rodriguez-Sanchez are with the Genetics Department, Hospital Universitario "Dr. José Eleuterio González" in Monterrey, Mexico.
Innov Clin Neurosci. 2022 Apr-Jun;19(4-6):78-86.
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 (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 (=0.0039), and those benefits remained and were further accentuated by Day 180 post-treatment (n=14; =<0.0001). Clinical benefit at Days 30 (=0.001; r= -0.51) and 180 (=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.
自闭症谱系障碍(ASD)是一组以社交和沟通缺陷为特征的神经发育性疾病,针对这些疾病的治疗方法有限。细胞疗法,包括鞘内注射骨髓单个核细胞(BM-MNC),可改善ASD患者的症状。根据《精神疾病诊断与统计手册》第四版修订版(DSM-IV-TR)标准诊断为ASD的24例患者接受了自体鞘内注射BM-MNC治疗,并在治疗后第30天(n = 24)和第180天(n = 14)使用儿童自闭症评定量表(CARS)评估临床效果。鞘内注射BM-MNC在治疗后第30天改善了临床结局(P = 0.0039),这些益处持续存在,并在治疗后第180天进一步增强(n = 14;P<=0.0001)。治疗后第30天(P = 0.001;r = -0.51)和第180天(P = 0.01;r = -0.60)的临床益处与表达分化簇133+(CD133+)表面标志物的假定BM干细胞群体的富集呈正相关。