hCT-MSCs for Children With Autism Spectrum Disorder (ASD)

Inclusion Criteria: 1. Age ≥ 2 years to ≤ 12 years (11 years, 364 days) at the time of consent 2. Confirmed clinical DSM-5 diagnosis of Autism Spectrum Disorder using the DSM-5 Checklist with a moderate severity level of ASD as reflected by SRS score ≥ 66 and CGI-S severity score of ≥ 4. 3. Fragile X testing performed and negative; CMA and/or whole exome sequencing performed and results not linked to autism diagnosis 4. Stable on current psychiatric medication regimen (dose and dosing schedule) for at least 2 months prior to infusion of study product 5. Normal absolute lymphocyte count (≥1500/uL) 6. Participant and parent/guardian are English speaking 7. Able to travel to Duke University up to four times (baseline, every two months for subsequent infusions, and 6 months after initial infusion), and parent/guardian is able to participate in interim surveys and interviews 8. Parental consent Exclusion Criteria: 1. General: 1. Review of medical records indicates ASD diagnosis not likely 2. Known diagnosis of any of the following coexisting psychiatric conditions: depression, bipolar disorder, schizophrenia, obsessive compulsive disorder associated with bipolar disorder, Tourette syndrome 3. Screening data suggests that participant would not be able to comply with the requirements of the study procedures as assessed by the study team 4. Family is unwilling or unable to commit to participation in all study-related assessments, including protocol follow up 5. Sibling is enrolled in this (Duke hCT-MSC) study 2. Genetic: 1. Records indicate that child has a known genetic syndrome such as (but not limited to) Fragile X syndrome, neurofibromatosis, Rett syndrome, tuberous sclerosis, PTEN mutation, cystic fibrosis, muscular dystrophy or a genetic defect definitively known to be associated with ASD 2. Evaluation by geneticist (performed locally as standard of care or remotely by the study geneticist via review of available data - minimally medical records, photos, Fragile X and CMA testing) indicates a genetic cause for ASD. 3. Infectious: 1. Known active CNS infection 2. Evidence of uncontrolled infection based on records or clinical assessment 3. Known HIV positivity 4. Medical: 1. Known metabolic disorder 2. Known abnormal thyroid function (patients with treated hypothyroidism with a normal TSH may be included) 3. Known mitochondrial dysfunction 4. History of unstable epilepsy or uncontrolled seizure disorder, infantile spasms, Lennox Gastaut syndrome, Dravet syndrome, or other similar chronic seizure disorder 5. Active malignancy or prior malignancy that was treated with chemotherapy 6. History of a primary immunodeficiency disorder 7. History of autoimmune cytopenias (i.e., ITP, AIHA) 8. Coexisting medical condition that would place the child at increased risk for complications of study procedures 9. Concurrent genetic or acquired disease or comorbidity(ies) that could require a future stem cell transplant 10. Significant sensory (e.g., blindness, deafness, uncorrected hearing impairment) or motor (e.g., cerebral palsy) impairment 11. Impaired renal or liver function as determined by serum creatinine \>1.5mg/dL or total bilirubin \>1.3mg/dL, except in patients with known Gilbert's disease 12. Significant hematologic abnormalities defined as: Hemoglobin \<10.0 g/dL, WBC \< 3,000 cells/mL, ALC \<1000/uL, Platelets \<150 x 10e9/uL 13. Evidence of clinically relevant physical dysmorphology indicative of a genetic syndrome as assessed by the PIs or other investigators, including a medical geneticist and psychiatrists trained in identifying dysmorphic features associated with neurodevelopmental conditions. 5. Current/Prior Therapy: a. History of prior cell therapy b. Current or prior use of IVIG or other anti-inflammatory medications with the exception of NSAIDs c. Current or prior immunosuppressive therapy i. No systemic steroid therapy that has lasted \>2 weeks, and no systemic steroids within 3 months prior to enrollment. Topical and inhaled steroids are permitted.