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用髓系来源的抑制细胞对抗婴儿感染。

Fighting infant infections with myeloid-derived suppressor cells.

出版信息

J Clin Invest. 2019 Oct 1;129(10):4080-4082. doi: 10.1172/JCI131649.

DOI:10.1172/JCI131649
PMID:31483288
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6763219/
Abstract

Recent work demonstrated a role for myeloid-derived suppressor cells (MDSCs) in the antimicrobial response in newborns, but the signals guiding their differentiation remained unknown. In this issue of the JCI, Liu et al. demonstrate that lactoferrin (LF) converts newborn neutrophils and monocytes to MDSCs via the low-density lipoprotein receptor-related protein-2 (LRP2) receptor and NF-κB activation. Due to their strong antimicrobial activity, adoptive transfer of MDSCs generated by in vitro culture with LF prolonged the survival of newborn mice with necrotizing enterocolitis, a severe pathology in preterm infants. These findings indicate a surprising protective role of MDSCs in newborns and demonstrate the potential of MDSC therapy for the treatment of infants with diseases associated with deregulated inflammation.

摘要

最近的研究表明,髓系来源的抑制细胞(MDSCs)在新生儿的抗菌反应中起作用,但指导其分化的信号仍然未知。在本期 JCI 中,刘等人表明乳铁蛋白(LF)通过低密度脂蛋白受体相关蛋白-2(LRP2)受体和 NF-κB 激活将新生中性粒细胞和单核细胞转化为 MDSCs。由于它们具有很强的抗菌活性,通过体外培养用 LF 生成的 MDSC 的过继转移延长了患有坏死性小肠结肠炎的新生小鼠的存活时间,坏死性小肠结肠炎是早产儿的一种严重疾病。这些发现表明 MDSCs 在新生儿中具有惊人的保护作用,并表明 MDSC 疗法治疗与炎症失调相关疾病的婴儿的潜力。

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本文引用的文献

1
Lactoferrin-induced myeloid-derived suppressor cell therapy attenuates pathologic inflammatory conditions in newborn mice.乳铁蛋白诱导的髓源抑制性细胞治疗可减轻新生小鼠的病理性炎症状态。
J Clin Invest. 2019 Oct 1;129(10):4261-4275. doi: 10.1172/JCI128164.
2
Melanoma Extracellular Vesicles Generate Immunosuppressive Myeloid Cells by Upregulating PD-L1 via TLR4 Signaling.黑色素瘤细胞外囊泡通过 TLR4 信号上调 PD-L1 产生免疫抑制性髓系细胞。
Cancer Res. 2019 Sep 15;79(18):4715-4728. doi: 10.1158/0008-5472.CAN-19-0053. Epub 2019 Jul 23.
3
Tumor-derived microRNAs induce myeloid suppressor cells and predict immunotherapy resistance in melanoma.肿瘤源性 microRNAs 诱导髓系抑制细胞,并预测黑色素瘤的免疫治疗耐药性。
J Clin Invest. 2018 Dec 3;128(12):5505-5516. doi: 10.1172/JCI98060. Epub 2018 Nov 5.
4
Plasticity and biological diversity of myeloid derived suppressor cells.髓系来源的抑制性细胞的可塑性和生物多样性。
Curr Opin Immunol. 2018 Apr;51:154-161. doi: 10.1016/j.coi.2018.03.015. Epub 2018 Mar 31.
5
Myeloid-derived suppressor cells coming of age.髓系来源的抑制细胞崭露头角。
Nat Immunol. 2018 Feb;19(2):108-119. doi: 10.1038/s41590-017-0022-x. Epub 2018 Jan 18.
6
Transitory presence of myeloid-derived suppressor cells in neonates is critical for control of inflammation.髓系来源的抑制性细胞在新生儿中的短暂存在对于控制炎症至关重要。
Nat Med. 2018 Feb;24(2):224-231. doi: 10.1038/nm.4467. Epub 2018 Jan 15.
7
Granulocytic myeloid-derived suppressor cells (GR-MDSC) accumulate in cord blood of preterm infants and remain elevated during the neonatal period.粒细胞髓系来源的抑制细胞(GR-MDSC)在早产儿的脐血中积聚,并在新生儿期保持升高。
Clin Exp Immunol. 2018 Mar;191(3):328-337. doi: 10.1111/cei.13059. Epub 2017 Oct 26.
8
Neonatal myeloid derived suppressor cells show reduced apoptosis and immunosuppressive activity upon infection with Escherichia coli.新生儿髓源性抑制细胞在感染大肠埃希菌后凋亡减少,免疫抑制活性降低。
Eur J Immunol. 2017 Jun;47(6):1009-1021. doi: 10.1002/eji.201646621. Epub 2017 May 26.
9
Necrotizing enterocolitis: new insights into pathogenesis and mechanisms.坏死性小肠结肠炎:发病机制的新见解
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