Affiliation:
1. Elizabeth Garrett Anderson Institute for Women's Health University College London London UK
2. Department of Clinical Science, Intervention and Technology Division of Obstetrics and Gynecology, Karolinska Institutet ANA Futura Huddinge Sweden
3. NIHR University College London Hospitals Biomedical Research Centre London UK
Abstract
AbstractObjectiveTo investigate the maternal and fetal safety of In utero stem cell transplantation (IUSCT).MethodsMedline®, Embase and Cochrane library (1967−2023) search for publications reporting IUSCT in humans. Two reviewers independently screened abstracts and full‐text papers.ResultsSixty six transplantation procedures in 52 fetuses were performed for haemoglobinopathies (n = 14), red cell/bleeding disorders (n = 4), immunodeficiencies (n = 15), storage disorders (n = 7), osteogenesis imperfecta (n = 2) and healthy fetuses (n = 10). The average gestational age was 18.9 weeks; of procedures reporting the injection route, cells were delivered by intraperitoneal (n = 37), intravenous (n = 19), or intracardiac (n = 4) injection or a combination (n = 3); most fetuses received one injection (n = 41). Haematopoietic (n = 40) or mesenchymal (n = 12) stem cells were delivered. The cell dose was inconsistently reported (range 1.8−3.3 × 109 cells total (n = 27); 2.7−5.0 × 109/kg estimated fetal weight (n = 17)). The acute fetal procedural complication rate was 4.5% (3/66); the acute fetal mortality rate was 3.0% (2/66). Neonatal survival was 69.2% (36/52). Immediate maternal and pregnancy outcomes were reported in only 30.8% (16/52) and 44.2% (23/52) of cases respectively. Four fetal/pregnancy outcomes would also classify as ≥ Grade 2 maternal adverse events.ConclusionsShort‐, medium‐, and long‐term maternal and fetal adverse events should be reported in all IUSCT studies.
Subject
Genetics (clinical),Obstetrics and Gynecology
Cited by
3 articles.
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