Impact of Intestinal Microbiota on Reconstitution of Circulating Monocyte, Dendritic Cell, and Natural Killer Cell Subsets in Adults Undergoing Single-Unit Cord Blood Transplantation

Takaaki Konuma , Chisato Kohara , Eri Watanabe , Shunsuke Takahashi , Genki Ozawa , Kentaro Inomata , Kei Suzuki , Motoko Mizukami , Etsuko Nagai , Motohito Okabe , Masamichi Isobe , Seiko Kato , Maki Oiwa-Monna , Satoshi Takahashi , Arinobu Tojo
{"title":"Impact of Intestinal Microbiota on Reconstitution of Circulating Monocyte, Dendritic Cell, and Natural Killer Cell Subsets in Adults Undergoing Single-Unit Cord Blood Transplantation","authors":"Takaaki Konuma ,&nbsp;Chisato Kohara ,&nbsp;Eri Watanabe ,&nbsp;Shunsuke Takahashi ,&nbsp;Genki Ozawa ,&nbsp;Kentaro Inomata ,&nbsp;Kei Suzuki ,&nbsp;Motoko Mizukami ,&nbsp;Etsuko Nagai ,&nbsp;Motohito Okabe ,&nbsp;Masamichi Isobe ,&nbsp;Seiko Kato ,&nbsp;Maki Oiwa-Monna ,&nbsp;Satoshi Takahashi ,&nbsp;Arinobu Tojo","doi":"10.1016/j.bbmt.2020.08.009","DOIUrl":null,"url":null,"abstract":"<div><p>The intestinal microbiota plays a fundamental role in the development of host innate immune cells, such as monocytes, dendritic cells (DCs), and natural killer (NK) cells. We examined the association between intestinal microbiota and subsequent immune reconstitution of circulating monocyte, DC, and NK cell subsets in 38 adult patients undergoing single-unit cord blood transplantation (CBT). A higher diversity of intestinal microbiota at 1 month was significantly associated with higher counts of plasmacytoid DCs at 7 months after CBT, as measured by the Chao1 index. Principal coordinate analysis of unweighted UniFrac distances showed significant differences between higher and lower classical monocyte reconstitution at 7 months post-CBT. The families <em>Neisseriaceae, Burkholderiaceae, Propionibacteriaceae</em>, and <em>Coriobacteriaceae</em> were increased in higher classical monocyte reconstitution at 7 months post-CBT, whereas the family <em>Bacteroidaceae</em> was increased in lower classical monocyte reconstitution at 7 months post-CBT. These data show that intestinal microbiota composition affects immune reconstitution of classical monocyte and plasmacytoid DCs following single-unit CBT.</p></div>","PeriodicalId":9165,"journal":{"name":"Biology of Blood and Marrow Transplantation","volume":null,"pages":null},"PeriodicalIF":4.3000,"publicationDate":"2020-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.bbmt.2020.08.009","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biology of Blood and Marrow Transplantation","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1083879120305012","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 1

Abstract

The intestinal microbiota plays a fundamental role in the development of host innate immune cells, such as monocytes, dendritic cells (DCs), and natural killer (NK) cells. We examined the association between intestinal microbiota and subsequent immune reconstitution of circulating monocyte, DC, and NK cell subsets in 38 adult patients undergoing single-unit cord blood transplantation (CBT). A higher diversity of intestinal microbiota at 1 month was significantly associated with higher counts of plasmacytoid DCs at 7 months after CBT, as measured by the Chao1 index. Principal coordinate analysis of unweighted UniFrac distances showed significant differences between higher and lower classical monocyte reconstitution at 7 months post-CBT. The families Neisseriaceae, Burkholderiaceae, Propionibacteriaceae, and Coriobacteriaceae were increased in higher classical monocyte reconstitution at 7 months post-CBT, whereas the family Bacteroidaceae was increased in lower classical monocyte reconstitution at 7 months post-CBT. These data show that intestinal microbiota composition affects immune reconstitution of classical monocyte and plasmacytoid DCs following single-unit CBT.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
在接受单单位脐带血移植的成人中,肠道微生物群对循环单核细胞、树突状细胞和自然杀伤细胞亚群重建的影响
肠道微生物群在宿主先天免疫细胞(如单核细胞、树突状细胞(dc)和自然杀伤细胞(NK))的发育中起着重要作用。我们研究了38例接受单单位脐带血移植(CBT)的成年患者肠道微生物群与循环单核细胞、DC细胞和NK细胞亚群随后的免疫重建之间的关系。根据Chao1指数测量,1个月时肠道微生物群多样性较高与CBT后7个月时浆细胞样dc计数较高显著相关。未加权UniFrac距离的主坐标分析显示,在cbt后7个月,较高和较低的经典单核细胞重构之间存在显著差异。在cbt后7个月,neisseraceae, burkholderaceae, Propionibacteriaceae和Coriobacteriaceae家族的经典单核细胞重建增加,而Bacteroidaceae家族的经典单核细胞重建在cbt后7个月增加。这些数据表明,肠道菌群组成影响单单位CBT后经典单核细胞和浆细胞样dc的免疫重建。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
CiteScore
6.60
自引率
0.00%
发文量
1061
审稿时长
3-6 weeks
期刊介绍: Biology of Blood and Marrow Transplantation publishes original research reports, reviews, editorials, commentaries, letters to the editor, and hypotheses and is the official publication of the American Society for Transplantation and Cellular Therapy. The journal focuses on current technology and knowledge in the interdisciplinary field of hematopoetic stem cell transplantation.
期刊最新文献
Table of Contents Editorial Board Goal-Oriented Monitoring of Cyclosporine Is Effective for Graft-versus-Host Disease Prevention after Hematopoietic Stem Cell Transplantation in Sickle Cell Disease and Thalassemia Major Early Mixed Lymphoid Donor/Host Chimerism is Associated with Improved Transplant Outcome in Patients with Primary or Secondary Myelofibrosis Real-World Issues and Potential Solutions in Hematopoietic Cell Transplantation during the COVID-19 Pandemic: Perspectives from the Worldwide Network for Blood and Marrow Transplantation and Center for International Blood and Marrow Transplant Research Health Services and International Studies Committee
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1