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

Publication ,  Journal Article
Zhu, Y; Yao, Z-C; Li, S; Ma, J; Wei, C; Yu, D; Stelzel, JL; Ni, BYX; Miao, Y; Van Batavia, K; Lu, X; Lin, J; Dai, Y; Kong, J; Shen, R ...
Published in: Nature communications
July 2025

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.

Duke Scholars

Published In

Nature communications

DOI

EISSN

2041-1723

ISSN

2041-1723

Publication Date

July 2025

Volume

16

Issue

1

Start / End Page

5707

Related Subject Headings

  • Tumor Microenvironment
  • RNA, Messenger
  • Neoplasms
  • Nanoparticles
  • Nanofibers
  • Mice, Inbred C57BL
  • Mice
  • Liposomes
  • Lipids
  • Immunotherapy
 

Citation

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Zhu, Y., Yao, Z.-C., Li, S., Ma, J., Wei, C., Yu, D., … Mao, H.-Q. (2025). An mRNA lipid nanoparticle-incorporated nanofiber-hydrogel composite for cancer immunotherapy. Nature Communications, 16(1), 5707. https://doi.org/10.1038/s41467-025-61299-8
Zhu, Yining, Zhi-Cheng Yao, Shuyi Li, Jingyao Ma, Christine Wei, Di Yu, Jessica L. Stelzel, et al. “An mRNA lipid nanoparticle-incorporated nanofiber-hydrogel composite for cancer immunotherapy.Nature Communications 16, no. 1 (July 2025): 5707. https://doi.org/10.1038/s41467-025-61299-8.
Zhu Y, Yao Z-C, Li S, Ma J, Wei C, Yu D, et al. An mRNA lipid nanoparticle-incorporated nanofiber-hydrogel composite for cancer immunotherapy. Nature communications. 2025 Jul;16(1):5707.
Zhu, Yining, et al. “An mRNA lipid nanoparticle-incorporated nanofiber-hydrogel composite for cancer immunotherapy.Nature Communications, vol. 16, no. 1, July 2025, p. 5707. Epmc, doi:10.1038/s41467-025-61299-8.
Zhu Y, Yao Z-C, Li S, Ma J, Wei C, Yu D, Stelzel JL, Ni BYX, Miao Y, Van Batavia K, Lu X, Lin J, Dai Y, Kong J, Shen R, Goodier KD, Liu X, Cheng L, Vuong I, Howard GP, Livingston NK, Choy J, Schneck JP, Doloff JC, Reddy SK, Hickey JW, Mao H-Q. An mRNA lipid nanoparticle-incorporated nanofiber-hydrogel composite for cancer immunotherapy. Nature communications. 2025 Jul;16(1):5707.

Published In

Nature communications

DOI

EISSN

2041-1723

ISSN

2041-1723

Publication Date

July 2025

Volume

16

Issue

1

Start / End Page

5707

Related Subject Headings

  • Tumor Microenvironment
  • RNA, Messenger
  • Neoplasms
  • Nanoparticles
  • Nanofibers
  • Mice, Inbred C57BL
  • Mice
  • Liposomes
  • Lipids
  • Immunotherapy