细胞哨兵:通过间充质干细胞和T淋巴细胞增强造血干细胞移植的存活和免疫防御。

IF 8.3 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL BMC Medicine Pub Date : 2025-03-18 DOI:10.1186/s12916-025-03987-2
Tzong-Shyuan Tai, Yun-Hsiang Chen, Chao-Ling Yao, Jiun-Han Lin, Yu-Shao Yang, Jai-Wen Shi, Li-Wen Fang, Duen-Wei Hsu, Shu-Chen Kuo, Shu-Ching Hsu
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引用次数: 0

摘要

背景:造血干细胞移植(HSCT)是治疗血液病如白血病、淋巴瘤和特异性免疫缺陷的重要方法。尽管它的疗效,挑战,如植入失败和延迟中性粒细胞再生仍然是显著的障碍。这些并发症导致细胞减少时间延长,感染和其他并发症的风险增加,发病率和死亡率升高。虽然间充质干细胞(MSCs)已知在支持造血中发挥重要作用,但MSCs与造血移植中其他细胞成分之间的确切机制和相互作用需要进一步研究。方法:为了解决这些挑战,我们探索了来自同一供者的异体脐带血造血干细胞(hsc)和活化T细胞以及第三方间充质干细胞的联合输注。该研究评估了这种三细胞疗法对中性粒细胞分化和功能的体外和体内的影响。使用呼吸道感染模型,与对照组相比,我们评估了人类中性粒细胞的积累、细胞因子分泌(IL-6和IL-8)、细菌清除率和总生存率。结果:三细胞治疗在体外和体内均能显著改善人造血干细胞向中性粒细胞的分化。在呼吸道感染模型中,与对照组相比,这种方法导致人类中性粒细胞积累增强,IL-6和IL-8分泌增加,细菌清除率提高,死亡率降低。这些发现强调了同种造血干细胞、间充质干细胞和活化T细胞之间在促进中性粒细胞产生和功能方面的协同相互作用。结论:我们的研究提出了一种新的治疗策略,结合异体造血干细胞、活化T细胞和第三方间充质干细胞来增强移植后中性粒细胞的产生和功能。这种方法不仅加速了中性粒细胞的再生,而且提高了对感染的抵抗力,为克服造血干细胞移植的移植挑战提供了一条有希望的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Cellular sentinels: empowering survival and immune defense in hematopoietic stem cell transplantation through mesenchymal stem cells and T lymphocytes.

Background: Hematopoietic stem cell transplantation (HSCT) is a critical treatment for hematologic disorders such as leukemia, lymphoma, and specific immune deficiencies. Despite its efficacy, challenges such as engraftment failure and delayed neutrophil regeneration remain significant barriers. These complications lead to prolonged cytopenia, increased risks of infections and other complications, and elevated morbidity and mortality rates. While mesenchymal stem cells (MSCs) are known to play essential roles in supporting hematopoiesis, the precise mechanisms and interactions between MSCs and other cellular components in HSCT require further investigation.

Methods: To address these challenges, we explored the combined infusion of allotype-cord blood hematopoietic stem cells (HSCs) and activated T cells from the same donor along with third-party MSCs. The study assessed the effects of this triple-cell therapy on neutrophil differentiation and function ex vivo and in vivo. Using a respiratory infection model, we evaluated the accumulation of human neutrophils, cytokine secretion (IL-6 and IL-8), bacterial clearance, and overall survival compared to control groups.

Results: The triple-cell therapy demonstrated a significant improvement in the differentiation of human HSCs into neutrophils both in ex vivo and in vivo. In the respiratory infection model, this approach resulted in enhanced accumulation of human neutrophils, increased secretion of IL-6 and IL-8, superior bacterial clearance, and reduced mortality rates compared to the control group. These findings highlight the synergistic interplay between allo-HSCs, MSCs, and activated T cells in promoting neutrophil production and function.

Conclusions: Our study presents a novel therapeutic strategy combining allo-HSCs, activated T cells, and third-party MSCs to enhance neutrophil production and functionality post-transplantation. This approach not only accelerates neutrophil regeneration but also improves resistance to infections, offering a promising avenue to overcome engraftment challenges in HSCT.

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来源期刊
BMC Medicine
BMC Medicine 医学-医学:内科
CiteScore
13.10
自引率
1.10%
发文量
435
审稿时长
4-8 weeks
期刊介绍: BMC Medicine is an open access, transparent peer-reviewed general medical journal. It is the flagship journal of the BMC series and publishes outstanding and influential research in various areas including clinical practice, translational medicine, medical and health advances, public health, global health, policy, and general topics of interest to the biomedical and sociomedical professional communities. In addition to research articles, the journal also publishes stimulating debates, reviews, unique forum articles, and concise tutorials. All articles published in BMC Medicine are included in various databases such as Biological Abstracts, BIOSIS, CAS, Citebase, Current contents, DOAJ, Embase, MEDLINE, PubMed, Science Citation Index Expanded, OAIster, SCImago, Scopus, SOCOLAR, and Zetoc.
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