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脐带血移植治疗婴儿型克拉伯病患儿

Transplantation of umbilical-cord blood in babies with infantile Krabbe's disease.

作者信息

Escolar Maria L, Poe Michele D, Provenzale James M, Richards Karen C, Allison June, Wood Susan, Wenger David A, Pietryga Daniel, Wall Donna, Champagne Martin, Morse Richard, Krivit William, Kurtzberg Joanne

机构信息

Program for Neurodevelopmental Function in Rare Disorders, Clinical Center for the Study of Development and Learning, University of North Carolina at Chapel Hill, Chapel Hill 27599-7255, USA.

出版信息

N Engl J Med. 2005 May 19;352(20):2069-81. doi: 10.1056/NEJMoa042604.

Abstract

BACKGROUND

Infantile Krabbe's disease produces progressive neurologic deterioration and death in early childhood. We hypothesized that transplantation of umbilical-cord blood from unrelated donors before the development of symptoms would favorably alter the natural history of the disease among newborns in whom the disease was diagnosed because of a family history. We compared the outcomes among these newborns with the outcomes among infants who underwent transplantation after the development of symptoms and with the outcomes in an untreated cohort of affected children.

METHODS

Eleven asymptomatic newborns (age range, 12 to 44 days) and 14 symptomatic infants (age range, 142 to 352 days) with infantile Krabbe's disease underwent transplantation of umbilical-cord blood from unrelated donors after myeloablative chemotherapy. Engraftment, survival, and neurodevelopmental function were evaluated longitudinally for four months to six years.

RESULTS

The rates of donor-cell engraftment and survival were 100 percent and 100 percent, respectively, among the asymptomatic newborns (median follow-up, 3.0 years) and 100 percent and 43 percent, respectively, among the symptomatic infants (median follow-up, 3.4 years). Surviving patients showed durable engraftment of donor-derived hematopoietic cells with restoration of normal blood galactocerebrosidase levels. Infants who underwent transplantation before the development of symptoms showed progressive central myelination and continued gains in developmental skills, and most had age-appropriate cognitive function and receptive language skills, but a few had mild-to-moderate delays in expressive language and mild-to-severe delays in gross motor function. Children who underwent transplantation after the onset of symptoms had minimal neurologic improvement.

CONCLUSIONS

Transplantation of umbilical-cord blood from unrelated donors in newborns with infantile Krabbe's disease favorably altered the natural history of the disease. Transplantation in babies after symptoms had developed did not result in substantive neurologic improvement.

摘要

背景

婴儿型克拉伯病会导致幼儿期进行性神经功能恶化并死亡。我们推测,在症状出现之前移植无关供者的脐带血,可能会改善因家族病史而被诊断出患有该病的新生儿的疾病自然病程。我们将这些新生儿的预后与出现症状后接受移植的婴儿的预后以及未接受治疗的患病儿童队列的预后进行了比较。

方法

11名无症状新生儿(年龄范围为12至44天)和14名有症状婴儿(年龄范围为142至352天)患有婴儿型克拉伯病,在接受清髓化疗后接受了无关供者的脐带血移植。对植入、生存和神经发育功能进行了长达4个月至6年的纵向评估。

结果

无症状新生儿(中位随访时间为3.0年)的供体细胞植入率和生存率分别为100%和100%,有症状婴儿(中位随访时间为3.4年)的供体细胞植入率和生存率分别为100%和43%。存活患者显示供体来源的造血细胞持久植入,血液中半乳糖脑苷脂酶水平恢复正常。在症状出现前接受移植的婴儿显示出中枢髓鞘形成进展以及发育技能持续提高,大多数婴儿具有与其年龄相符的认知功能和接受性语言技能,但少数婴儿在表达性语言方面有轻度至中度延迟,在粗大运动功能方面有轻度至重度延迟。症状出现后接受移植的儿童神经功能改善甚微。

结论

对患有婴儿型克拉伯病的新生儿移植无关供者的脐带血可改善该病的自然病程。症状出现后对婴儿进行移植并未导致实质性的神经功能改善。

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