造血干细胞移植后的单核细胞重建和肠道微生物群组成

Clinical Hematology International Pub Date : 2020-11-23 eCollection Date: 2020-12-01 DOI:10.2991/chi.k.201108.002
Sejal Morjaria, Allen W Zhang, Sohn Kim, Jonathan U Peled, Simone Becattini, Eric R Littmann, Eric G Pamer, Michael C Abt, Miguel-Angel Perales
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引用次数: 0

摘要

背景:单核细胞是先天性免疫系统的重要细胞成分,它能帮助宿主有效对抗各种传染性病原体。造血细胞移植(HCT)会导致一过性的单核细胞耗竭,但调节单核细胞群恢复的因素尚不完全清楚。在这项研究中,我们探讨了胃肠道微生物群的组成是否与 HCT 后单核细胞平衡的恢复有关:我们对 18 名自体或异体 HCT 受者进行了一项单中心、前瞻性、试验性研究。在 HCT 住院期间,我们收集了每位患者的连续血液和粪便样本。利用 16S rRNA 基因测序分析了肠道微生物群,并通过流式细胞分析鉴定了单核细胞群的表型组成:结果:单核细胞重建在 HCT 后出现了动态波动,而且随着时间的推移,患者之间的单核细胞频率出现了巨大差异。单核细胞绝对数量和亚群的恢复在不同的移植类型和调理强度下显示出显著的差异性;在这一小型队列中未观察到与微生物群组成的关系:在这项试验性研究中,微生物群组成与单核细胞稳态之间的关系尚未确定。然而,我们发现了临床因素与单核细胞造血干细胞移植后重建之间的多变量关联。我们的研究结果鼓励对肠道微生物群及其与免疫重建之间的联系进行进一步的纵向监测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Monocyte Reconstitution and Gut Microbiota Composition after Hematopoietic Stem Cell Transplantation.

Monocyte Reconstitution and Gut Microbiota Composition after Hematopoietic Stem Cell Transplantation.

Monocyte Reconstitution and Gut Microbiota Composition after Hematopoietic Stem Cell Transplantation.

Monocyte Reconstitution and Gut Microbiota Composition after Hematopoietic Stem Cell Transplantation.

Background: Monocytes are an essential cellular component of the innate immune system that support the host's effectiveness to combat a range of infectious pathogens. Hemopoietic cell transplantation (HCT) results in transient monocyte depletion, but the factors that regulate recovery of monocyte populations are not fully understood. In this study, we investigated whether the composition of the gastrointestinal microbiota is associated with the recovery of monocyte homeostasis after HCT.

Methods: We performed a single-center, prospective, pilot study of 18 recipients of either autologous or allogeneic HCT. Serial blood and stool samples were collected from each patient during their HCT hospitalization. Analysis of the gut microbiota was done using 16S rRNA gene sequencing, and flow cytometric analysis was used to characterize the phenotypic composition of monocyte populations.

Results: Dynamic fluctuations in monocyte reconstitution occurred after HCT, and large differences were observed in monocyte frequency among patients over time. Recovery of absolute monocyte counts and subsets showed significant variability across the heterogeneous transplant types and conditioning intensities; no relationship to the microbiota composition was observed in this small cohort.

Conclusion: In this pilot study, a relationship between the microbiota composition and monocyte homeostasis could not be firmly established. However, we identify multivariate associations between clinical factors and monocyte reconstitution post-HCT. Our findings encourage further longitudinal surveillance of the intestinal microbiome and its link to immune reconstitution.

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