<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Wang G</submitter><funding>Basic Research Special Project of Key Research Projects in Higher Education Institutions in Henan Province</funding><funding>National Natural Science Foundation of China</funding><funding>Program for Innovative Research Team (in Science and Technology) in University of Henan Province</funding><funding>Natural Science Foundation of Henan</funding><pagination>e12281</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12713043</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12(47)</volume><pubmed_abstract>Rheumatoid arthritis (RA) is closely associated with intestinal microbiota dysbiosis, highlighting the therapeutic potential of targeting the microbiota-gut-joint axis. Current interventions often overlook the cascade nature of reactive oxygen species (ROS) generation in driving intestinal and systemic inflammation. Herein, a valence-engineered CeO&lt;sub>X&lt;/sub>-based nanozyme with self-cascade catalytic activity is developed, mimicking sequential oxidase-superoxide dismutase-peroxidase functions to enable continuous ROS scavenging while minimizing oxygen generation. By precisely tuning Ce&lt;sup>3+&lt;/sup>/Ce&lt;sup>4+&lt;/sup> ratios from 0.27 to 0.93 through Au deposition (0.23 wt.%→5.2 wt.%), Dual functionality is achieved: 1) enhanced oxygen vacancy generation (71.4%) for efficient ROS scavenging </pubmed_abstract><journal>Advanced science (Weinheim, Baden-Wurttemberg, Germany)</journal><pubmed_title>Structure-Tailoring Cerium Nanozymes with Self-Cascade ROS Scavenging Catalysis Modulate the Microbiota-Gut-Joint Axis for Rheumatoid Arthritis Therapy.</pubmed_title><pmcid>PMC12713043</pmcid><funding_grant_id>22107089</funding_grant_id><funding_grant_id>242300421210</funding_grant_id><funding_grant_id>24ZX009</funding_grant_id><funding_grant_id>23IRTSTHN002</funding_grant_id><funding_grant_id>52271251</funding_grant_id><funding_grant_id>U21A20314</funding_grant_id><pubmed_authors>Ding S</pubmed_authors><pubmed_authors>Zhang X</pubmed_authors><pubmed_authors>Xiao Y</pubmed_authors><pubmed_authors>Zhang H</pubmed_authors><pubmed_authors>Guo W</pubmed_authors><pubmed_authors>Yan D</pubmed_authors><pubmed_authors>Wang G</pubmed_authors><pubmed_authors>Ma J</pubmed_authors><pubmed_authors>Ni T</pubmed_authors><pubmed_authors>Zhu B</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Structure-Tailoring Cerium Nanozymes with Self-Cascade ROS Scavenging Catalysis Modulate the Microbiota-Gut-Joint Axis for Rheumatoid Arthritis Therapy.</name><description>Rheumatoid arthritis (RA) is closely associated with intestinal microbiota dysbiosis, highlighting the therapeutic potential of targeting the microbiota-gut-joint axis. Current interventions often overlook the cascade nature of reactive oxygen species (ROS) generation in driving intestinal and systemic inflammation. Herein, a valence-engineered CeO&lt;sub>X&lt;/sub>-based nanozyme with self-cascade catalytic activity is developed, mimicking sequential oxidase-superoxide dismutase-peroxidase functions to enable continuous ROS scavenging while minimizing oxygen generation. By precisely tuning Ce&lt;sup>3+&lt;/sup>/Ce&lt;sup>4+&lt;/sup> ratios from 0.27 to 0.93 through Au deposition (0.23 wt.%→5.2 wt.%), Dual functionality is achieved: 1) enhanced oxygen vacancy generation (71.4%) for efficient ROS scavenging </description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Dec</publication><modification>2026-06-08T05:20:36.847Z</modification><creation>2026-06-08T03:08:46.094Z</creation></dates><accession>S-EPMC12713043</accession><cross_references><pubmed>41024355</pubmed><doi>10.1002/advs.202512281</doi></cross_references></HashMap>