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An mRNA lipid nanoparticle-incorporated nanofiber-hydrogel composite for cancer immunotherapy

Author

Listed:
  • Yining Zhu

    (Johns Hopkins University School of Medicine
    Johns Hopkins University
    Johns Hopkins University School of Medicine)

  • Zhi-Cheng Yao

    (Johns Hopkins University
    Johns Hopkins University School of Medicine
    Johns Hopkins University)

  • Shuyi Li

    (Johns Hopkins University
    Johns Hopkins University School of Medicine)

  • Jingyao Ma

    (Johns Hopkins University
    Johns Hopkins University School of Medicine
    Johns Hopkins University)

  • Christine Wei

    (Johns Hopkins University School of Medicine
    Johns Hopkins University
    Johns Hopkins University School of Medicine)

  • Di Yu

    (Johns Hopkins University School of Medicine
    Johns Hopkins University
    Johns Hopkins University School of Medicine)

  • Jessica L. Stelzel

    (Johns Hopkins University School of Medicine
    Johns Hopkins University
    Johns Hopkins University School of Medicine)

  • Bobby Y. X. Ni

    (Duke University)

  • Yang Miao

    (Duke University)

  • Kyra Van Batavia

    (Duke University)

  • Xiaoya Lu

    (Johns Hopkins University
    Johns Hopkins University School of Medicine
    Johns Hopkins University)

  • Jinghan Lin

    (Johns Hopkins University
    Johns Hopkins University School of Medicine
    Johns Hopkins University)

  • Yifan Dai

    (University of North Carolina at Chapel Hill)

  • Jiayuan Kong

    (Johns Hopkins University
    Johns Hopkins University School of Medicine
    Johns Hopkins University)

  • Ruochen Shen

    (Johns Hopkins University School of Medicine
    Johns Hopkins University
    Johns Hopkins University School of Medicine)

  • Kailei D. Goodier

    (Johns Hopkins University
    Johns Hopkins University School of Medicine
    Johns Hopkins University)

  • Xiang Liu

    (Johns Hopkins University
    Johns Hopkins University School of Medicine)

  • Leonardo Cheng

    (Johns Hopkins University School of Medicine
    Johns Hopkins University
    Johns Hopkins University School of Medicine)

  • Ivan Vuong

    (Johns Hopkins University School of Medicine
    Johns Hopkins University
    Johns Hopkins University School of Medicine)

  • Gregory P. Howard

    (Johns Hopkins University School of Medicine
    Johns Hopkins University
    Johns Hopkins University School of Medicine)

  • Natalie K. Livingston

    (Johns Hopkins University School of Medicine
    Johns Hopkins University
    Johns Hopkins University School of Medicine
    Johns Hopkins University School of Medicine)

  • Joseph Choy

    (Johns Hopkins University
    Johns Hopkins University School of Medicine
    Johns Hopkins University)

  • Jonathan P. Schneck

    (Johns Hopkins University
    Johns Hopkins University School of Medicine
    Johns Hopkins University School of Medicine
    Johns Hopkins University School of Medicine)

  • Joshua C. Doloff

    (Johns Hopkins University School of Medicine
    Johns Hopkins University
    Johns Hopkins University School of Medicine
    Johns Hopkins University)

  • Sashank K. Reddy

    (Johns Hopkins University School of Medicine
    Johns Hopkins University
    Johns Hopkins University School of Medicine)

  • John W. Hickey

    (Duke University)

  • Hai-Quan Mao

    (Johns Hopkins University School of Medicine
    Johns Hopkins University
    Johns Hopkins University School of Medicine
    Johns Hopkins University)

Abstract

Hydrogel materials have emerged as versatile platforms for various biomedical applications. Notably, the engineered nanofiber-hydrogel composite (NHC) has proven effective in mimicking the soft tissue extracellular matrix, facilitating substantial recruitment of host immune cells and the formation of a local immunostimulatory microenvironment. Leveraging this feature, here we report an mRNA lipid nanoparticle (LNP)-incorporated NHC microgel matrix, termed LiNx, by incorporating LNPs loaded with mRNA encoding tumour antigens. Harnessing the high transfection efficiency of LNPs in antigen-presenting cells, LiNx demonstrates substantial levels of immune cell recruitment, antigen expression and presentation, and cellular interaction. These attributes collectively create an immunostimulating microenvironment and yield a potent immune response with a single dose at a level comparable to the conventional three-dose LNP immunization protocol. Further investigation reveals that the LiNx generates not only high levels of Th1 and Th2 responses, but also a distinct Type 17 T helper cell response critical for bolstering antitumour efficacy. Our findings elucidate the mechanism underlying LiNx’s role in potentiating antigen-specific immune responses, presenting a strategy for cancer immunotherapy.

Suggested Citation

  • Yining Zhu & Zhi-Cheng Yao & Shuyi Li & Jingyao Ma & Christine Wei & Di Yu & Jessica L. Stelzel & Bobby Y. X. Ni & Yang Miao & Kyra Van Batavia & Xiaoya Lu & Jinghan Lin & Yifan Dai & Jiayuan Kong & R, 2025. "An mRNA lipid nanoparticle-incorporated nanofiber-hydrogel composite for cancer immunotherapy," Nature Communications, Nature, vol. 16(1), pages 1-16, December.
  • Handle: RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-61299-8
    DOI: 10.1038/s41467-025-61299-8
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