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Engineering antiviral immune-like systems for autonomous virus detection and inhibition in mice

Author

Listed:
  • Yidan Wang

    (East China Normal University
    Chongqing Institute of East China Normal University)

  • Ying Xu

    (East China Normal University)

  • Chee Wah Tan

    (Duke-NUS Medical School)

  • Longliang Qiao

    (East China Normal University)

  • Wan Ni Chia

    (Duke-NUS Medical School)

  • Hongyi Zhang

    (Tongji University)

  • Qin Huang

    (East China Normal University)

  • Zhenqiang Deng

    (East China Normal University)

  • Ziwei Wang

    (East China Normal University)

  • Xi Wang

    (Chinese Academy of Sciences
    University of Chinese Academy of Sciences)

  • Xurui Shen

    (Chinese Academy of Sciences
    University of Chinese Academy of Sciences)

  • Canyu Liu

    (University of Chinese Academy of Sciences
    Chinese Academy of Sciences)

  • Rongjuan Pei

    (Chinese Academy of Sciences)

  • Yuanxiao Liu

    (East China Normal University)

  • Shuai Xue

    (East China Normal University
    ETH Zurich)

  • Deqiang Kong

    (East China Normal University)

  • Danielle E. Anderson

    (Duke-NUS Medical School)

  • Fengfeng Cai

    (Tongji University)

  • Peng Zhou

    (Chinese Academy of Sciences)

  • Lin-Fa Wang

    (Duke-NUS Medical School
    SingHealth Duke-NUS Global Health Institute)

  • Haifeng Ye

    (East China Normal University)

Abstract

The ongoing COVID-19 pandemic has demonstrated that viral diseases represent an enormous public health and economic threat to mankind and that individuals with compromised immune systems are at greater risk of complications and death from viral diseases. The development of broad-spectrum antivirals is an important part of pandemic preparedness. Here, we have engineer a series of designer cells which we term autonomous, intelligent, virus-inducible immune-like (ALICE) cells as sense-and-destroy antiviral system. After developing a destabilized STING-based sensor to detect viruses from seven different genera, we have used a synthetic signal transduction system to link viral detection to the expression of multiple antiviral effector molecules, including antiviral cytokines, a CRISPR-Cas9 module for viral degradation and the secretion of a neutralizing antibody. We perform a proof-of-concept study using multiple iterations of our ALICE system in vitro, followed by in vivo functionality testing in mice. We show that dual output ALICESaCas9+Ab system delivered by an AAV-vector inhibited viral infection in herpetic simplex keratitis (HSK) mouse model. Our work demonstrates that viral detection and antiviral countermeasures can be paired for intelligent sense-and-destroy applications as a flexible and innovative method against virus infection.

Suggested Citation

  • Yidan Wang & Ying Xu & Chee Wah Tan & Longliang Qiao & Wan Ni Chia & Hongyi Zhang & Qin Huang & Zhenqiang Deng & Ziwei Wang & Xi Wang & Xurui Shen & Canyu Liu & Rongjuan Pei & Yuanxiao Liu & Shuai Xue, 2022. "Engineering antiviral immune-like systems for autonomous virus detection and inhibition in mice," Nature Communications, Nature, vol. 13(1), pages 1-18, December.
  • Handle: RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-35425-9
    DOI: 10.1038/s41467-022-35425-9
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    References listed on IDEAS

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    2. Hiroki Ishikawa & Zhe Ma & Glen N. Barber, 2009. "STING regulates intracellular DNA-mediated, type I interferon-dependent innate immunity," Nature, Nature, vol. 461(7265), pages 788-792, October.
    3. Camilo Mora & Tristan McKenzie & Isabella M. Gaw & Jacqueline M. Dean & Hannah Hammerstein & Tabatha A. Knudson & Renee O. Setter & Charlotte Z. Smith & Kira M. Webster & Jonathan A. Patz & Erik C. Fr, 2022. "Over half of known human pathogenic diseases can be aggravated by climate change," Nature Climate Change, Nature, vol. 12(9), pages 869-875, September.
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