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Uremic Clearance Granules Regulate Immune Equilibrium via Gut Microbiome to Alleviate Chronic Renal Failure

  • Qian Huang (Co-first Author)
  • , Zhuowen Liang (Co-first Author)
  • , Yuqing Cui (Co-first Author)
  • , Jianxin Diao
  • , Tianshu Zhou
  • , Lei Shi
  • , Zhixin Deng
  • , Rushang Wang
  • , Haitao Yuan
  • , Kun Chen
  • , Ying Du*
  • , Ali Chen*
  • , Jiayun Chen*
  • , Wei Xiao*
  • *Corresponding author for this work

Research output: Journal Publications and Reviews › RGC 21 - Publication in refereed journal › peer-review

4 Downloads (CityUHK Scholars)

Abstract

Chronic renal failure (CRF) is the common end point of various chronic kidney diseases, and there is currently no specific drug for CRF. Effectively halting its progression remains a clinical challenge. Gut microbiota disorders are a key factor influencing immune dysfunction in chronic kidney disease patients. Intervening in gut microbiota to improve immune regulatory function in patients could serve as a new strategy for treating CRF with Traditional Chinese Medicine. Uremic Clearance Granules (UCG), a Traditional Chinese Medicine formulation, effectively attenuate CRF progression, but their active components and mechanisms remain undefined. This study investigates how UCG mitigate CRF via coordinated regulation of gut microbiota, metabolites, and the T helper 17 cells / regulatory T cell axis. Using an adenine-induced CRF mouse model, we combined gut microbiota depletion, fecal microbiota transplantation, 16S rRNA sequencing, and metabolomics to delineate the gut–kidney interactions underlying UCG efficacy. Flow cytometry quantified immune cell profiles in blood, and microbial intervention experiments verified the therapeutic role of Bifidobacterium animalis (B. animalis). In this study, we found that UCG treatment alleviated renal injury, reduced intestinal permeability, and up-regulated intestinal barrier markers. Microbiota depletion and fecal microbiota transplantation demonstrated that UCG’s renoprotective effects depend on gut microbial modulation. Specifically, UCG ameliorates CRF through gut–kidney axis remodeling by enhancing B. animalis abundance and sophocarpine, thereby rebalancing T helper 17/regulatory T immunity and preserving renal function. These findings identify a microbiota-dependent immunometabolic mechanism for UCG and highlight a potential therapeutic strategy for CRF via the drug–microbiota axis. © 2026 Qian Huang et al.
Original languageEnglish
Article number0342
Number of pages18
JournalBiomaterials Research
Volume30
Online published30 Mar 2026
DOIs
Publication statusPublished - 2026

Bibliographical note

Full text of this publication does not contain sufficient affiliation information. Related Research Unit(s) information for this record is supplemented by the author(s) concerned.

Funding

This work was financially supported by the National Key Research and Development Program of China (Early warning and systematic effective intervention of sub-health state with abnormal glucose and lipid metabolism [No. 2023YFC3606200]), the National Natural Science Foundation of China (Nos. 82474501 and 82505161), the Basic and Applied Basic Research Fund-Natural Science Foundation of Guangdong (No. 2023A1515011483), and Innovation Team Project-Scientific Research Project of Ordinary Universities in Guangdong Province, China (No. 2023KCXTD019).

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Publisher's Copyright Statement

  • This full text is made available under CC-BY 4.0. https://creativecommons.org/licenses/by/4.0/

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