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April 5, 2026Cancer Research0 citations

Abstract 3386: MESHCAP (exogenous microbiota and humanized mice for lung cancer): Towards an innovative preclinical model for testing immunotherapies

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PMPierre MontagneUJUlrich JarryMHMathilde Harel

Key Points

  • To create a preclinical model combining humanized immune systems and microbiota to improve immunotherapy outcomes in lung cancer.
  • Developed the MESHCAP xenograft model using circulating tumor cells from SCLC patients.
  • Humanized mice by injecting human CD34+ hematopoietic stem cells for immune system adaptation.
  • Cultured a beneficial bacterial consortium for gut microbiota stabilization in the model.
  • Used 16S sequencing to monitor bacterial presence post-inoculation.
  • Implanted CTC-derived xenografts (CDXs) into doubly humanized mice for therapy testing.
  • Preliminary data indicate a significant interaction between humanized microbiota and the immune system.
  • Achieved sustained presence of inoculated bacteria in fecal samples over a month.
  • Successfully generated chimeric immune systems in immunodeficient mice for SCLC studies.

Abstract

Abstract Small cell lung cancer (SCLC) is the most aggressive subtype of lung cancer. The recent combination of chemotherapy with immune checkpoint inhibitors shows a response in only 10 to 15% of patients. At the same time, numerous studies highlight the impact of gut microbiota composition on the response to immunotherapy. To address these current challenges, we are developing a xenograft model called "MESHCAP." This model involves grafting circulating tumor cells (CTCs) from SCLC patients onto mice that have been humanized for both their immune system and their gut microbiota. With its unique dual humanization, this model will allow us to take into account the influence of the microbiota when testing new therapeutic strategies. Based on the literature, we have identified a bacterial consortium hypothesized to be beneficial for the response to immunotherapy. This consortium is cultured in the laboratory and then inoculated into immunodeficient mice whose endogenous microbiota has been previously depleted by antibiotic treatment. We are able to detect the presence of these bacteria in the feces by 16S sequencing more than a month after inoculation. In parallel, we have humanized the immune system of immunodeficient mice by injecting human CD34+ hematopoietic stem cells. This engraftment results in chimerism of the mouse immune system. Currently, we are developing the generation of doubly humanized mice for both the microbiota and the immune system. Preliminary data suggest a cross-talk between the humanized microbiota and the human immune system. In our laboratory, we routinely isolate CTCs from patients diagnosed with CTC. We then inject them subcutaneously to generate CDXs (CTC-derived xenografts). It is these CDXs that we will implant into our doubly humanized mouse model to investigate the impact of the microbiota and immune system on therapies (e.g. immunotherapy). Citation Format: Pierre Montagne, Ulrich Jarry, Mathilde Harel, Laetitia Martinetti, Anna Le Mée, Charles Ricordel, Ahmad FAILI, Samer Kayal, Rémy Pedeux, Marwan Touati, Valentin Quiniou, Hang-Phuong Pham. MESHCAP (exogenous microbiota and humanized mice for lung cancer): Towards an innovative preclinical model for testing immunotherapies abstract. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 3386.

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Montagne et al. (2026) studied this question.

synapsesocial.com/papers/69d1fca7a79560c99a0a2480https://doi.org/10.1158/1538-7445.am2026-3386
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