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人羊膜干细胞预防性治疗可改善新生儿败血症幸存者的长期认知障碍。

Prophylactic Therapy with Human Amniotic Fluid Stem Cells Improves Long-Term Cognitive Impairment in Rat Neonatal Sepsis Survivors.

机构信息

Department of Obstetrics & Gynecology, Keio University School of Medicine, Tokyo 160-8582, Japan.

StemCell Institute Inc., Tokyo 105-0004, Japan.

出版信息

Int J Mol Sci. 2020 Dec 16;21(24):9590. doi: 10.3390/ijms21249590.

DOI:10.3390/ijms21249590
PMID:33339379
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7766081/
Abstract

A systemic inflammatory response induces multiple organ dysfunction and results in poor long-term neurological outcomes in neonatal sepsis. However, there is no effective therapy for treating or preventing neonatal sepsis besides antibiotics and supportive care. Therefore, a novel strategy to improve neonatal sepsis-related morbidity and mortality is desirable. Recently, we reported that prophylactic therapy with human amniotic stem cells (hAFSCs) improved survival in a rat model of lipopolysaccharide (LPS)-induced neonatal sepsis through immunomodulation. Besides improving the mortality, increasing survival without major morbidities is an important goal of neonatal intensive care for neonatal sepsis. This study investigated long-term neurological outcomes in neonatal sepsis survivors treated with hAFSCs using the LPS-induced neonatal sepsis model in rats. We found that prophylactic therapy with hAFSCs improved spatial awareness and memory-based behavior in neonatal sepsis survivors at adolescence in rats. The treatment suppressed acute reactive gliosis and subsequently reduced astrogliosis in the hippocampal region over a long period of assessment. To the best of our knowledge, this is the first report that proves the concept that hAFSC treatment improves cognitive impairment in neonatal sepsis survivors. We demonstrate the efficacy of hAFSC therapy in improving the mortality and morbidity associated with neonatal sepsis.

摘要

全身炎症反应会导致多器官功能障碍,并导致新生儿败血症的长期神经预后不良。然而,除了抗生素和支持性治疗外,目前尚无治疗或预防新生儿败血症的有效方法。因此,需要一种新的策略来改善与新生儿败血症相关的发病率和死亡率。最近,我们报道称,通过免疫调节,预防性应用人羊膜干细胞(hAFSCs)可改善脂多糖(LPS)诱导的新生大鼠败血症模型中的存活率。除了提高死亡率外,提高无重大并发症的存活率是新生儿败血症新生儿重症监护的一个重要目标。本研究使用 LPS 诱导的新生大鼠败血症模型,研究了 hAFSCs 治疗的新生儿败血症幸存者的长期神经结局。我们发现,预防性应用 hAFSCs 可改善 LPS 诱导的新生败血症大鼠青春期幸存者的空间意识和基于记忆的行为。该治疗方法在长期评估中抑制了急性反应性神经胶质增生,并随后减少了海马区的星形胶质增生。据我们所知,这是第一个证明 hAFSC 治疗可改善新生儿败血症幸存者认知障碍的概念的报告。我们证明了 hAFSC 治疗在改善与新生儿败血症相关的死亡率和发病率方面的疗效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dbc/7766081/2e8fa159d2fa/ijms-21-09590-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dbc/7766081/2f9a972919ea/ijms-21-09590-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dbc/7766081/885a35cc4257/ijms-21-09590-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dbc/7766081/ff23596712da/ijms-21-09590-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dbc/7766081/2e8fa159d2fa/ijms-21-09590-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dbc/7766081/2f9a972919ea/ijms-21-09590-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dbc/7766081/885a35cc4257/ijms-21-09590-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dbc/7766081/ff23596712da/ijms-21-09590-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dbc/7766081/2e8fa159d2fa/ijms-21-09590-g004.jpg

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