High‐Lactate‐Metabolizing Photosynthetic Bacteria Reprogram Tumor Immune Microenvironment

Author:

Ma Yichuan1,Hu Yujing2,Liu Huifang2,Li Xiaoya2,Li Yuanhang2,Zhao Yu2,Zhang Qi1,Zhang Ziyang2,Leng Qingqing2,Luo Li34,Li Lanya34,Dai Yunlu5,Chen Guojun6,Zhang Jinchao1ORCID,Li Zhenhua34ORCID

Affiliation:

1. College of Chemistry & Materials Science State Key Laboratory of New Pharmaceutical Preparations and Excipients Chemical Biology Key Laboratory of Hebei Province Key Laboratory of Medicinal Chemistry and Molecular Diagnosis of Ministry of Education Hebei University Baoding 071002 China

2. College of Pharmaceutical Science Hebei University Baoding 071002 China

3. The Tenth Affiliated Hospital Southern Medical University Dongguan Guangdong 523059 China

4. Guangdong Provincial Key Laboratory of Cardiac Function and Microcirculation Guangzhou 510515 China

5. Cancer Centre and Institute of Translational Medicine Faculty of Health Sciences University of Macau Macau SAR 999078 China

6. Department of Biomedical Engineering McGill University Montreal QC H3G 0B1 Canada

Abstract

AbstractThe 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.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Hebei Province

Publisher

Wiley

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