Biohybrid nanorobots induce lactate isomer conversion to reverse the immune environment and promote tumor therapy

Tumor cell glycolysis produces high levels of l-lactate (l-LA), creating an immunosuppressive microenvironment that enhances tumor stemness and impairs the efficacy of cancer therapies. Current strategies to reduce l-LA are limited by physical barriers in solid tumors and resource waste. This study presents an intelligent nanorobot that not only enhances tumor targeting and deep penetration but also reprograms the tumor immune microenvironment to convert l-LA into immunostimulatory d-lactate (d-LA). The nanorobot uses gold nanoparticles to bridge palladium (Pd) nanozymes and <i>Lactobacillus crispatus</i>-derived outer membrane vesicles (CMVs). Pd nanozymes catalyze H<sub>2</sub>O<sub>2</sub> into O<sub>2</sub>, facilitating deep tumor penetration, whereas the acidic tumor microenvironment activates Pd nanozymes to produce hydroxyl radicals (·OH), inducing immunogenic cell death. CMVs, which are rich in d-lactate dehydrogenase and artificially introduce lactate oxidase, catalyze the conversion of l-LA to d-LA, reversing its immunosuppressive effects. Preclinical models demonstrate potent antitumor effects, enhancing the immune response and reshaping the tumor microbiome.

Authors

Institutions

Publication Details

Journal
Science Advances
Published
2025-11-14
DOI
https://doi.org/10.1126/sciadv.adz8419
Citations
1
Primary Topic
Nanoplatforms for cancer theranostics
Type
article
Field-Weighted Citation Impact
0.67

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Biohybrid nanorobots induce lactate isomer conversion to reverse the immune environment and promote tumor therapy

Jiamin Ye, Li Wang, Yaoguang She, Jiacheng Shi et al.
1 citations
Science Advances
Nanoplatforms for cancer theranostics
0.67
article

Biohybrid nanorobots induce lactate isomer conversion to reverse the immune environment and promote tumor therapy

Jiamin Ye, Li Wang, Yaoguang She, Jiacheng Shi, Yueyue Fan, Xiaoyuan Ji, Gaoli Niu, Ruiyan Li, Yong Kang, Yiwen Yang
article en
1 citations

Abstract

Tumor cell glycolysis produces high levels of l-lactate (l-LA), creating an immunosuppressive microenvironment that enhances tumor stemness and impairs the efficacy of cancer therapies. Current strategies to reduce l-LA are limited by physical barriers in solid tumors and resource waste. This study presents an intelligent nanorobot that not only enhances tumor targeting and deep penetration but also reprograms the tumor immune microenvironment to convert l-LA into immunostimulatory d-lactate (d-LA). The nanorobot uses gold nanoparticles to bridge palladium (Pd) nanozymes and <i>Lactobacillus crispatus</i>-derived outer membrane vesicles (CMVs). Pd nanozymes catalyze H<sub>2</sub>O<sub>2</sub> into O<sub>2</sub>, facilitating deep tumor penetration, whereas the acidic tumor microenvironment activates Pd nanozymes to produce hydroxyl radicals (·OH), inducing immunogenic cell death. CMVs, which are rich in d-lactate dehydrogenase and artificially introduce lactate oxidase, catalyze the conversion of l-LA to d-LA, reversing its immunosuppressive effects. Preclinical models demonstrate potent antitumor effects, enhancing the immune response and reshaping the tumor microbiome.

Science AdvancesVol. 11(46)
Tianjin University (CN), Chinese PLA General Hospital (CN), Jiaozuo University (CN), Tianjin Medical University (CN)
National Natural Science Foundation of China, Tianjin University
Openalex Percentile: Top 25%
Nanoplatforms for cancer theranostics
0.67
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.