Evidence map›Paper›PMID 42562136›Full record

ArticleCellular and molecular gastroenterology and hepatology2026

Dysbiosis-Associated Lysophosphatidic Acid Primes Immune Checkpoint Inhibitor-Induced Intestinal Barrier Dysfunction via the Lysophosphatidic Acid Receptor 2-Myosin Light Chain Kinase Axis.

Lei Xiong, Jianshang Huang, Qiuyuan Liu, Hanqi Xia, Nina Zhu, Weizhen Xiang, Wentao Xu, Yunsheng Dong, Rumeng Zhu, Yiran Han and 10 more

Abstract read
In one paragraph

Article in Cellular and molecular gastroenterology and hepatology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

20 authors.

Lei XiongLaboratory of Molecular Biology, and Department of Biochemistry, School of Basic Medical Science, Innovation and Entrepreneurship Laboratory for College Students, Anhui Medical University, Hefei, Anhui, China.
Jianshang HuangLaboratory of Molecular Biology, and Department of Biochemistry, School of Basic Medical Science, Innovation and Entrepreneurship Laboratory for College Students, Anhui Medical University, Hefei, Anhui, China.
Qiuyuan LiuDepartment of Gastroenterology, First Affiliated Hospital of Anhui Medical University, Hefei, China.
Hanqi XiaDepartment of Oncology, The First Affiliated Hospital of Anhui Medical University, Key Laboratory of Anti-Inflammatory and Immune Medicine (Anhui Medical University), Ministry of Education, Inflammation and Immune-Mediated Diseases Laboratory of Anhui Province, Hefei, Anhui, China.
Nina ZhuLaboratory of Molecular Biology, and Department of Biochemistry, School of Basic Medical Science, Innovation and Entrepreneurship Laboratory for College Students, Anhui Medical University, Hefei, Anhui, China.
Weizhen XiangDepartment of Gastroenterology, First Affiliated Hospital of Anhui Medical University, Hefei, China.
Wentao XuDepartment of Oncology, The First Affiliated Hospital of Anhui Medical University, Key Laboratory of Anti-Inflammatory and Immune Medicine (Anhui Medical University), Ministry of Education, Inflammation and Immune-Mediated Diseases Laboratory of Anhui Province, Hefei, Anhui, China.
Yunsheng DongDepartment of Oncology, The First Affiliated Hospital of Anhui Medical University, Key Laboratory of Anti-Inflammatory and Immune Medicine (Anhui Medical University), Ministry of Education, Inflammation and Immune-Mediated Diseases Laboratory of Anhui Province, Hefei, Anhui, China.
Rumeng ZhuLaboratory of Molecular Biology, and Department of Biochemistry, School of Basic Medical Science, Innovation and Entrepreneurship Laboratory for College Students, Anhui Medical University, Hefei, Anhui, China.
Yiran HanLaboratory of Molecular Biology, and Department of Biochemistry, School of Basic Medical Science, Innovation and Entrepreneurship Laboratory for College Students, Anhui Medical University, Hefei, Anhui, China.
Abduxukur RahmanLaboratory of Molecular Biology, and Department of Biochemistry, School of Basic Medical Science, Innovation and Entrepreneurship Laboratory for College Students, Anhui Medical University, Hefei, Anhui, China.
Huiqing XuLaboratory of Molecular Biology, and Department of Biochemistry, School of Basic Medical Science, Innovation and Entrepreneurship Laboratory for College Students, Anhui Medical University, Hefei, Anhui, China.
Weiwei XieDepartment of Digestive Medicine, The Second Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.
Zehua LuoLaboratory Animal Platform, Institute of Artificial Intelligence Hefei Comprehensive National Science Center, Hefei, Anhui, China.
Wei HeLaboratory of Molecular Biology, and Department of Biochemistry, School of Basic Medical Science, Innovation and Entrepreneurship Laboratory for College Students, Anhui Medical University, Hefei, Anhui, China.
Jerrold R TurnerDepartment of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts.
Yubao ZhouDepartment of Digestive Medicine, The Second Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China. Electronic address: zhouyubao@fy.ahmu.edu.cn.
Ruolei HuLaboratory of Molecular Biology, and Department of Biochemistry, School of Basic Medical Science, Innovation and Entrepreneurship Laboratory for College Students, Anhui Medical University, Hefei, Anhui, China. Electronic address: huruolei@ahmu.edu.cn.
Hua WangDepartment of Oncology, The First Affiliated Hospital of Anhui Medical University, Key Laboratory of Anti-Inflammatory and Immune Medicine (Anhui Medical University), Ministry of Education, Inflammation and Immune-Mediated Diseases Laboratory of Anhui Province, Hefei, Anhui, China. Electronic address: wanghua@ahmu.edu.cn.
Li ZuoLaboratory of Molecular Biology, and Department of Biochemistry, School of Basic Medical Science, Innovation and Entrepreneurship Laboratory for College Students, Anhui Medical University, Hefei, Anhui, China; The Second Affiliated Hospital of Anhui Medical University, Heifei, Anhui, China; Center for Experimental Animals, Anhui Medical University, Hefei, Anhui, China. Electronic address: zuoli@ahmu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND &

aimsImmune checkpoint inhibitor therapy is frequently limited by severe gastrointestinal toxicity. Although the immune mechanisms driving late-stage, overt mucosal inflammation are increasingly recognized, the early microbiota-metabolic events that prime epithelial barrier dysfunction remain poorly defined.

methodsWe employed an integrated multiomics approach in a murine model of early immune checkpoint inhibitor-induced injury, with validation in a clinical cohort of patients with immune checkpoint inhibitor colitis. Mechanisms were investigated using in vitro receptor screening, genetically engineered mice with altered myosin light chain kinase 1 activity, and pharmacologic intervention with repurposed low-dose tacrolimus. Subcutaneous melanoma models were utilized to evaluate the relationship between barrier modulation and antitumor outcomes.

resultsEarly immune checkpoint inhibitor treatment induced a distinct dysbiotic state characterized by Pseudomonadota expansion, which was associated with the accumulation of bioactive lysophosphatidic acid-a metabolic signature also observed in human patients. Mechanistically, we identified lysophosphatidic acid receptor 2 as the key epithelial sensor that transduces this metabolic signal into pathological myosin light chain kinase 1 activation, driving the priming phase of barrier dysfunction. Genetic ablation of myosin light chain kinase 1 prevented this early barrier loss and was associated with improved tumor control and favorable regional immune alterations. Conversely, constitutive activation of myosin light chain kinase 1 exacerbated barrier disruption, which correlated with accelerated tumor progression and a systemic immunosuppressive shift. Furthermore, repurposing low-dose tacrolimus as a selective modulator to disrupt FKBP8-dependent myosin light chain kinase 1 recruitment effectively mitigated barrier injury without dampening antitumor responses.

conclusionsThe dysbiosis-associated lysophosphatidic acid-lysophosphatidic acid receptor 2-myosin light chain kinase axis acts as an early metabolic trigger for the priming phase of immune checkpoint inhibitor-induced barrier dysfunction. Modulating this upstream initiation step provides a temporal and mechanism-based strategy to uncouple intestinal toxicity from anti-tumor efficacy.

Indexed as

Immune Checkpoint InhibitorsIntestinal BarrierLysophosphatidic AcidMyosin Light Chain Kinase

Identifiers

PMID42562136
PMCPMC13584131

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.