• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

肠相关淋巴组织:微生物群驱动的 B 细胞免疫中枢。

Gut-associated lymphoid tissue: a microbiota-driven hub of B cell immunity.

机构信息

Department of Translational Medicine - Human Immunology, Lund University, J Waldenströms gata 35, Malmö, Sweden; Department of Clinical Immunology and Transfusion Medicine, Sahlgrenska University Hospital, Region Västra Götaland, Gothenburg, Sweden.

Peter Gorer Department of Immunobiology, King's College London, Guy's Hospital Campus, St Thomas' Street, London SE1 9RT, UK.

出版信息

Trends Immunol. 2024 Mar;45(3):211-223. doi: 10.1016/j.it.2024.01.006. Epub 2024 Feb 23.

DOI:10.1016/j.it.2024.01.006
PMID:38402045
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11227984/
Abstract

The diverse gut microbiota, which is associated with mucosal health and general wellbeing, maintains gut-associated lymphoid tissues (GALT) in a chronically activated state, including sustainment of germinal centers in a context of high antigenic load. This influences the rules for B cell engagement with antigen and the potential consequences. Recent data have highlighted differences between GALT and other lymphoid tissues. For example, GALT propagates IgA responses against glycans that show signs of having been generated in germinal centers. Other findings suggest that humans are among those species where GALT supports the diversification, propagation, and possibly selection of systemic B cells. Here, we review novel findings that identify GALT as distinctive, and able to support these processes.

摘要

肠道微生物群的多样性与黏膜健康和整体健康有关,使肠道相关淋巴组织 (GALT) 处于慢性激活状态,包括在高抗原负荷的情况下维持生发中心。这影响了 B 细胞与抗原结合的规则和潜在的后果。最近的数据强调了 GALT 与其他淋巴组织之间的差异。例如,GALT 对表现出生发中心生成迹象的聚糖产生 IgA 反应。其他研究结果表明,人类是支持 GALT 支持系统 B 细胞多样化、传播和可能选择的物种之一。在这里,我们回顾了一些新的发现,这些发现确定了 GALT 的独特性,并能够支持这些过程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e516/11227984/b082b172936f/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e516/11227984/b50763db7e3b/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e516/11227984/2eaabf969be4/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e516/11227984/725911d5f325/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e516/11227984/b082b172936f/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e516/11227984/b50763db7e3b/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e516/11227984/2eaabf969be4/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e516/11227984/725911d5f325/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e516/11227984/b082b172936f/gr4.jpg

相似文献

1
Gut-associated lymphoid tissue: a microbiota-driven hub of B cell immunity.肠相关淋巴组织:微生物群驱动的 B 细胞免疫中枢。
Trends Immunol. 2024 Mar;45(3):211-223. doi: 10.1016/j.it.2024.01.006. Epub 2024 Feb 23.
2
IgA-producing plasma cells originate from germinal centers that are induced by B-cell receptor engagement in humans.产生 IgA 的浆细胞来源于生发中心,生发中心由人类 B 细胞受体结合诱导产生。
Gastroenterology. 2011 Mar;140(3):947-56. doi: 10.1053/j.gastro.2010.12.005. Epub 2010 Dec 11.
3
Function of mucosa-associated lymphoid tissue in antibody formation.黏膜相关淋巴组织在抗体形成中的作用。
Immunol Invest. 2010;39(4-5):303-55. doi: 10.3109/08820131003680369.
4
Intestinal IgA synthesis: a primitive form of adaptive immunity that regulates microbial communities in the gut.肠道IgA合成:一种调节肠道微生物群落的适应性免疫原始形式。
Curr Top Microbiol Immunol. 2006;308:137-53. doi: 10.1007/3-540-30657-9_6.
5
Generation of gut-homing IgA-secreting B cells by intestinal dendritic cells.肠道树突状细胞生成归巢至肠道的分泌IgA的B细胞。
Science. 2006 Nov 17;314(5802):1157-60. doi: 10.1126/science.1132742.
6
B cells and the intestinal microbiome in time, space and place.B 细胞与肠道微生物组在时间、空间和位置上的相互作用。
Semin Immunol. 2023 Sep;69:101806. doi: 10.1016/j.smim.2023.101806. Epub 2023 Jul 18.
7
B cell recruitment and selection in mouse GALT germinal centers.小鼠肠道相关淋巴组织生发中心中的B细胞募集与选择
Curr Top Microbiol Immunol. 2006;308:155-71. doi: 10.1007/3-540-30657-9_7.
8
Role of commensal bacteria in development of gut-associated lymphoid tissues and preimmune antibody repertoire.共生细菌在肠道相关淋巴组织发育和免疫前抗体库形成中的作用。
J Immunol. 2004 Jan 15;172(2):1118-24. doi: 10.4049/jimmunol.172.2.1118.
9
Individual neuropeptides regulate gut-associated lymphoid tissue integrity, intestinal immunoglobulin A levels, and respiratory antibacterial immunity.单个神经肽可调节肠道相关淋巴组织的完整性、肠道免疫球蛋白A水平以及呼吸道抗菌免疫力。
JPEN J Parenter Enteral Nutr. 2000 Sep-Oct;24(5):261-8; discussion 268-9. doi: 10.1177/0148607100024005261.
10
Is there evidence that the gut contributes to mucosal immunity in humans?是否有证据表明肠道对人类的黏膜免疫有贡献?
JPEN J Parenter Enteral Nutr. 2007 May-Jun;31(3):246-58. doi: 10.1177/0148607107031003246.

引用本文的文献

1
Gut-Brain Axis in Mood Disorders: A Narrative Review of Neurobiological Insights and Probiotic Interventions.情绪障碍中的肠-脑轴:神经生物学见解与益生菌干预的叙述性综述
Biomedicines. 2025 Jul 26;13(8):1831. doi: 10.3390/biomedicines13081831.
2
Advancing Nigerian Indigenous Poultry Health and Production, Use of Probiotics as Viable Alternatives to Antibiotics: A Review.推进尼日利亚本土家禽健康与生产:益生菌作为抗生素可行替代品的应用综述
Antibiotics (Basel). 2025 Aug 21;14(8):846. doi: 10.3390/antibiotics14080846.
3
Combined Hyaluronic Acid Nanobioconjugates Impair CD44-Signaling for Effective Treatment Against Obesity: A Review of Comparison with Other Actors.

本文引用的文献

1
The transcription factor ZEB2 drives the formation of age-associated B cells.转录因子 ZEB2 驱动与年龄相关的 B 细胞的形成。
Science. 2024 Jan 26;383(6681):413-421. doi: 10.1126/science.adf8531. Epub 2024 Jan 25.
2
Spatial transcriptomics of B cell and T cell receptors reveals lymphocyte clonal dynamics.B 细胞和 T 细胞受体的空间转录组学揭示了淋巴细胞克隆动力学。
Science. 2023 Dec 8;382(6675):eadf8486. doi: 10.1126/science.adf8486.
3
B cell immune profiles in dysbiotic vermiform appendixes of pancreatic cancer patients.胰腺癌患者肠道失调阑尾中的 B 细胞免疫特征。
联合透明质酸纳米生物共轭物通过损害CD44信号传导实现对肥胖症的有效治疗:与其他作用物的比较综述
Int J Nanomedicine. 2025 Aug 21;20:10101-10126. doi: 10.2147/IJN.S529250. eCollection 2025.
4
A model of early-life interactions between the gut microbiome and adaptive immunity provides insights into the ontogeny of immune tolerance.肠道微生物群与适应性免疫之间早期生命相互作用的模型为免疫耐受的个体发生提供了见解。
PLoS Biol. 2025 Aug 14;23(8):e3003263. doi: 10.1371/journal.pbio.3003263. eCollection 2025 Aug.
5
Gut microbiota in gastric cancer: from pathogenesis to precision medicine.胃癌中的肠道微生物群:从发病机制到精准医学
Front Microbiol. 2025 Jul 30;16:1606924. doi: 10.3389/fmicb.2025.1606924. eCollection 2025.
6
Microbiome in Neuroblastoma: A Virgin Island in the World of Onco-Microbiome.神经母细胞瘤中的微生物组:肿瘤微生物组领域的一片处女地。
Cells. 2025 Aug 7;14(15):1218. doi: 10.3390/cells14151218.
7
Exploring the relationship between intestinal immunity and obesity: A bibliometric and knowledge-map analysis.探索肠道免疫与肥胖之间的关系:文献计量学与知识图谱分析
Medicine (Baltimore). 2025 Aug 8;104(32):e43790. doi: 10.1097/MD.0000000000043790.
8
Modulation of oral vaccine efficacy by the gut microbiota.肠道微生物群对口服疫苗效力的调节作用。
NPJ Vaccines. 2025 Aug 1;10(1):179. doi: 10.1038/s41541-025-01240-8.
9
Secretory IgA dysfunction underlies poor prognosis in -infected colorectal cancer.分泌型IgA功能障碍是感染性结直肠癌预后不良的潜在原因。
Gut Microbes. 2025 Dec;17(1):2528428. doi: 10.1080/19490976.2025.2528428. Epub 2025 Jul 16.
10
Immune Cell Characteristics in a Gut-Kidney Axis-Induced Mouse Model of IgA Nephropathy: The Upregulated Dendritic Cells and Neutrophils.肠道-肾脏轴诱导的IgA肾病小鼠模型中的免疫细胞特征:树突状细胞和中性粒细胞上调
J Inflamm Res. 2025 Jul 1;18:8579-8592. doi: 10.2147/JIR.S519521. eCollection 2025.
Front Immunol. 2023 Nov 10;14:1230306. doi: 10.3389/fimmu.2023.1230306. eCollection 2023.
4
B cell diversification in gut-associated lymphoid tissues: From birds to humans.肠道相关淋巴组织中 B 细胞的多样化:从鸟类到人类。
J Exp Med. 2023 Nov 6;220(11). doi: 10.1084/jem.20231501. Epub 2023 Oct 12.
5
Macrophage and neutrophil heterogeneity at single-cell spatial resolution in human inflammatory bowel disease.人类炎症性肠病中单细胞空间分辨率下的巨噬细胞和中性粒细胞异质性。
Nat Commun. 2023 Jul 26;14(1):4506. doi: 10.1038/s41467-023-40156-6.
6
M cell maturation and cDC activation determine the onset of adaptive immune priming in the neonatal Peyer's patch.M 细胞成熟和 cDC 活化决定新生儿派尔集合淋巴结适应性免疫启动的时机。
Immunity. 2023 Jun 13;56(6):1220-1238.e7. doi: 10.1016/j.immuni.2023.04.002. Epub 2023 May 1.
7
Immune subset-committed proliferating cells populate the human foetal intestine throughout the second trimester of gestation.免疫亚群定向增殖细胞在妊娠中期的整个阶段都存在于人类胎儿肠道中。
Nat Commun. 2023 Mar 10;14(1):1318. doi: 10.1038/s41467-023-37052-4.
8
T-independent responses to polysaccharides in humans mobilize marginal zone B cells prediversified against gut bacterial antigens.人类对多糖的 T 细胞非依赖应答可动员边缘区 B 细胞,这些细胞预先针对肠道细菌抗原多样化。
Sci Immunol. 2023 Jan 27;8(79):eade1413. doi: 10.1126/sciimmunol.ade1413.
9
A close-up on the expanding landscape of CD21-/low B cells in humans.聚焦人类中 CD21-/低 B 细胞的扩展景观。
Clin Exp Immunol. 2022 Dec 31;210(3):217-229. doi: 10.1093/cei/uxac103.
10
Peyer's patch T17 cells are dispensable for gut IgA responses to oral immunization.派尔集合淋巴结 T17 细胞对于口服免疫诱导肠道 IgA 应答并非必需。
Sci Immunol. 2022 Jul;7(73):eabc5500. doi: 10.1126/sciimmunol.abc5500. Epub 2022 Jul 1.