High-Lactate-Metabolizing Photosynthetic Bacteria Reprogram Tumor Immune Microenvironment

© 2024 Wiley‐VCH GmbH.

Bibliographische Detailangaben
Veröffentlicht in:Advanced materials (Deerfield Beach, Fla.). - 1998. - 36(2024), 36 vom: 24. Sept., Seite e2405930
1. Verfasser: Ma, Yichuan (VerfasserIn)
Weitere Verfasser: Hu, Yujing, Liu, Huifang, Li, Xiaoya, Li, Yuanhang, Zhao, Yu, Zhang, Qi, Zhang, Ziyang, Leng, Qingqing, Luo, Li, Li, Lanya, Dai, Yunlu, Chen, Guojun, Zhang, Jinchao, Li, Zhenhua
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2024
Zugriff auf das übergeordnete Werk:Advanced materials (Deerfield Beach, Fla.)
Schlagworte:Journal Article bacteria biomaterials cancer immunotherapy lactate consumption tumor microenvironment Lactic Acid 33X04XA5AT
Beschreibung
Zusammenfassung:© 2024 Wiley‐VCH GmbH.
The elevated levels of lactate in tumor tissue play a pivotal role in fostering an immunosuppressive microenvironment. Therefore, efficiently reducing lactate levels to reprogram tumor immune microenvironment (TIM) is considered a crucial step for boosted immunotherapy. Here, a high-lactate-metabolizing photosynthetic bacteria (LAB-1) is selectively screened for TIM reprogramming, which then improves the efficacy of tumor immunotherapy. The culture medium for LAB-1 screening is initially developed through an orthogonal experiment, simulating the tumor microenvironment (TME) and utilizing lactate as the sole organic carbon source. As demonstrated in a murine 4T1 model, LAB-1 colonizes the TME selectively, resulting in a significant reduction in lactate levels and a subsequent increase in pH values within the tumor tissue. Furthermore, single-cell RNA sequencing analysis reveals that LAB-1 effectively reprograms the TIM, thereby enhancing the effectiveness of antitumor immune therapy. This approach of utilizing lactate-consuming bacteria represents a potent tool for augmenting tumor immunotherapy efficiency
Beschreibung:Date Completed 18.09.2024
Date Revised 18.09.2024
published: Print-Electronic
Citation Status MEDLINE
ISSN:1521-4095
DOI:10.1002/adma.202405930