Sagar Rachel, David Anna L
Elizabeth Garrett Anderson Institute for Women's Health, University College London, London, WC1E 6AU, UK.
Elizabeth Garrett Anderson Institute for Women's Health, University College London, London, WC1E 6AU, UK; National Institute for Health and Care Research, University College London Hospitals NHS Foundation Trust Biomedical Research Centre, 149 Tottenham Court Road, London, W1T 7DN, UK.
Best Pract Res Clin Obstet Gynaecol. 2024 Dec;97:102542. doi: 10.1016/j.bpobgyn.2024.102542. Epub 2024 Sep 11.
Advances in ultrasound and prenatal diagnosis are leading an expansion in the options for parents whose fetus is identified with a congenital disease. Obstetric diseases such as pre-eclampsia and fetal growth restriction may also be amenable to intervention to improve maternal and neonatal outcomes. Advanced Medicinal Therapeutic Products such as stem cell, gene, enzyme and protein therapies are most commonly being investigated as the trajectory of treatment for severe genetic diseases moves toward earlier intervention. Theoretical benefits include prevention of in utero damage, smaller treatment doses compared to postnatal intervention, use of fetal circulatory shunts and induction of immune tolerance. New systematic terminology can capture adverse maternal and fetal adverse events to improve safe trial conduct. First-in-human clinical trials are now beginning to generate results with a focus on safety first and efficacy second. If successful, these trials will transform the care of fetuses with severe early-onset congenital disease.
超声和产前诊断技术的进步,为那些胎儿被诊断患有先天性疾病的父母带来了更多选择。诸如先兆子痫和胎儿生长受限等产科疾病,也可能适合进行干预,以改善孕产妇和新生儿的结局。随着严重遗传疾病的治疗方向朝着早期干预发展,干细胞、基因、酶和蛋白质疗法等先进药物治疗产品正受到最为广泛的研究。理论上的益处包括预防子宫内损伤、与出生后干预相比使用更小的治疗剂量、利用胎儿循环分流以及诱导免疫耐受。新的系统术语能够涵盖孕产妇和胎儿的不良事件,以改善试验的安全实施。首次人体临床试验现已开始产生结果,重点是安全第一,疗效第二。如果试验成功,这些试验将改变患有严重早发性先天性疾病胎儿的护理方式。