Nanodisc-Forming Polymers as TLR7/8 Agonist-Conjugated Immunotherapy Agents

Amphiphilic polymers can solubilize membrane proteins in what is coined native lipid nanodiscs, although their potential as drug delivery platforms is mostly unexplored. Herein, we covalently attached a Toll-like receptor 7/8 agonist to poly(acrylic acid- co -styrene) to generate a multimodal cancer immunotherapy platform (AASTY-TLR7/8 ag. ) that acts as a loco-regional Toll-like receptor 7/8 agonist depot and as a nanodisc-driven in situ immunization platform. We show that AASTY-TLR7/8 ag. therapy translates into tumor growth inhibition in CT26 and other murine cancer models, with the induction of immune memory, synergy with anti-PD-1, and limited on-target/off-tumor toxicity. By formulating nanodiscs from cancer cell membranes in vitro, we also observed that subcutaneous injection in mice leads to rapid distribution in lymph nodes and immune activation of dendritic cells, highlighting the broader potential of AASTY-TLR7/8 ag. as a tool for immunization.

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Publication Details

Journal
Biomacromolecules
Published
2026-07-16
DOI
https://doi.org/10.1021/acs.biomac.6c00611
Primary Topic
RNA Interference and Gene Delivery
Type
article
Field-Weighted Citation Impact
0.00
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article

Nanodisc-Forming Polymers as TLR7/8 Agonist-Conjugated Immunotherapy Agents

John H. Klich, Sven Weller, Jerry Yan, Caitlin L. Maikawa et al.
Biomacromolecules
RNA Interference and Gene Delivery
article

Nanodisc-Forming Polymers as TLR7/8 Agonist-Conjugated Immunotherapy Agents

John H. Klich, Sven Weller, Jerry Yan, Caitlin L. Maikawa, Anton A. A. Autzen, Laura O. Marchard, Charalampos Sideris, Ciara F. Pugh, Unnur J. Björgvinsdóttir, Anders E. Hansen, Kristoffer H. Johansen, Ditte E. Jæhger, Thomas L. Andresen, Henriette E. Autzen, Neil J. Borthwick
article en

Abstract

Amphiphilic polymers can solubilize membrane proteins in what is coined native lipid nanodiscs, although their potential as drug delivery platforms is mostly unexplored. Herein, we covalently attached a Toll-like receptor 7/8 agonist to poly(acrylic acid- co -styrene) to generate a multimodal cancer immunotherapy platform (AASTY-TLR7/8 ag. ) that acts as a loco-regional Toll-like receptor 7/8 agonist depot and as a nanodisc-driven in situ immunization platform. We show that AASTY-TLR7/8 ag. therapy translates into tumor growth inhibition in CT26 and other murine cancer models, with the induction of immune memory, synergy with anti-PD-1, and limited on-target/off-tumor toxicity. By formulating nanodiscs from cancer cell membranes in vitro, we also observed that subcutaneous injection in mice leads to rapid distribution in lymph nodes and immune activation of dendritic cells, highlighting the broader potential of AASTY-TLR7/8 ag. as a tool for immunization.

Biomacromolecules
University of Copenhagen (DK), Brigham and Women's Hospital (US), Harvard University (US), Technical University of Denmark (DK), Stanford University (US)
Good health and well-being
Openalex Percentile: Top 14%
RNA Interference and Gene Delivery
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