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Ultrasound-controllable engineered bacteria for cancer immunotherapy

Author

Listed:
  • Mohamad H. Abedi

    (California Institute of Technology
    University of Washington)

  • Michael S. Yao

    (California Institute of Technology)

  • David R. Mittelstein

    (California Institute of Technology)

  • Avinoam Bar-Zion

    (California Institute of Technology)

  • Margaret B. Swift

    (California Institute of Technology)

  • Audrey Lee-Gosselin

    (California Institute of Technology)

  • Pierina Barturen-Larrea

    (California Institute of Technology)

  • Marjorie T. Buss

    (California Institute of Technology)

  • Mikhail G. Shapiro

    (California Institute of Technology
    California Institute of Technology)

Abstract

Rapid advances in synthetic biology are driving the development of genetically engineered microbes as therapeutic agents for a multitude of human diseases, including cancer. The immunosuppressive microenvironment of solid tumors, in particular, creates a favorable niche for systemically administered bacteria to engraft and release therapeutic payloads. However, such payloads can be harmful if released outside the tumor in healthy tissues where the bacteria also engraft in smaller numbers. To address this limitation, we engineer therapeutic bacteria to be controlled by focused ultrasound, a form of energy that can be applied noninvasively to specific anatomical sites such as solid tumors. This control is provided by a temperature-actuated genetic state switch that produces lasting therapeutic output in response to briefly applied focused ultrasound hyperthermia. Using a combination of rational design and high-throughput screening we optimize the switching circuits of engineered cells and connect their activity to the release of immune checkpoint inhibitors. In a clinically relevant cancer model, ultrasound-activated therapeutic microbes successfully turn on in situ and induce a marked suppression of tumor growth. This technology provides a critical tool for the spatiotemporal targeting of potent bacterial therapeutics in a variety of biological and clinical scenarios.

Suggested Citation

  • Mohamad H. Abedi & Michael S. Yao & David R. Mittelstein & Avinoam Bar-Zion & Margaret B. Swift & Audrey Lee-Gosselin & Pierina Barturen-Larrea & Marjorie T. Buss & Mikhail G. Shapiro, 2022. "Ultrasound-controllable engineered bacteria for cancer immunotherapy," Nature Communications, Nature, vol. 13(1), pages 1-11, December.
  • Handle: RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-29065-2
    DOI: 10.1038/s41467-022-29065-2
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    References listed on IDEAS

    as
    1. Christopher A. Voigt, 2020. "Synthetic biology 2020–2030: six commercially-available products that are changing our world," Nature Communications, Nature, vol. 11(1), pages 1-6, December.
    2. Daniel S. Leventhal & Anna Sokolovska & Ning Li & Christopher Plescia & Starsha A. Kolodziej & Carey W. Gallant & Rudy Christmas & Jian-Rong Gao & Michael J. James & Andres Abin-Fuentes & Munira Momin, 2020. "Immunotherapy with engineered bacteria by targeting the STING pathway for anti-tumor immunity," Nature Communications, Nature, vol. 11(1), pages 1-15, December.
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    Cited by:

    1. Pei Liu & Josquin Foiret & Yinglin Situ & Nisi Zhang & Aris J. Kare & Bo Wu & Marina N. Raie & Katherine W. Ferrara & Lei S. Qi, 2023. "Sonogenetic control of multiplexed genome regulation and base editing," Nature Communications, Nature, vol. 14(1), pages 1-11, December.
    2. Xiaotu Ma & Xiaolong Liang & Yao Li & Qingqing Feng & Keman Cheng & Nana Ma & Fei Zhu & Xinjing Guo & Yale Yue & Guangna Liu & Tianjiao Zhang & Jie Liang & Lei Ren & Xiao Zhao & Guangjun Nie, 2023. "Modular-designed engineered bacteria for precision tumor immunotherapy via spatiotemporal manipulation by magnetic field," Nature Communications, Nature, vol. 14(1), pages 1-22, December.
    3. Dinh-Huy Nguyen & Ari Chong & Yeongjin Hong & Jung-Joon Min, 2023. "Bioengineering of bacteria for cancer immunotherapy," Nature Communications, Nature, vol. 14(1), pages 1-5, December.

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