# Programmable Antigen‐Specific Immunity via Self‐Adjuvanting Nanovaccines Co‐Delivering Immune Modulators

**Authors:** Keita Ito, Yoshiyuki Manabe, Shino Ohshima, Masatoshi Maeki, Manabu Tokeshi, Hiroshi Inaba, Kazunori Matsuura, Kazuya Kabayama, Yoshie Kametani, Koichi Fukase

PMC · DOI: 10.1002/anie.202520474 · Angewandte Chemie (International Ed. in English) · 2025-12-17

## TL;DR

Researchers developed a new vaccine platform that boosts immune responses against cancer by combining antigens and adjuvants in tiny nanoparticles.

## Contribution

A self-adjuvanting nanovaccine platform was developed using cationic lipid nanoparticles and immune modulators to enhance antigen-specific immunity.

## Key findings

- The nanovaccines elicited strong immune responses in humanized mouse models.
- The platform allows precise modulation of antigen-specific immune responses.
- The iLiNP device enabled size-controlled nanoparticle formulation for vaccine development.

## Abstract

Cancer peptide vaccines harness the host immune system to generate tumor‐specific immune responses, offering potential for treating metastatic cancers and preventing recurrence. However, the limited immunogenicity of peptide antigens restricts their clinical efficacy, necessitating strategies to enhance their potency. One promising approach involves the conjugation of antigens with adjuvants to elicit antigen‐specific immune responses, thereby creating self‐adjuvanting vaccines. In this study, we developed an improved platform for such vaccines. Specifically, the antigenic CH401 peptide was conjugated with the adjuvant (Pam3CSK4) and formulated into cationic lipid nanoparticles (LNPs) smaller than 100 nm to facilitate uptake by immune cells, with supplemental adjuvants incorporated to modulate immune responses. Notably, the microflow device iLiNP enabled precise, size‐controlled LNP formulation from various components, supporting the systematic evolution of the self‐adjuvanting vaccine platform. These vaccine candidates demonstrated enhanced immunogenicity, enabling precise modulation of immune responses in an antigen‐specific manner. Notably, these vaccines elicited potent immune responses in humanized mouse models. Overall, this strategy represents a next‐generation self‐adjuvanting vaccine platform, capable of both enhancing and fine‐tuning antigen‐specific immune responses, holding great promise for innovative vaccine development.

The self‐adjuvanting vaccine—comprising a covalent conjugate of antigen and adjuvant—was formulated into cationic lipid nanoparticles smaller than 100 nm to facilitate uptake by immune cells, with supplemental adjuvants incorporated to modulate immune responses. Notably, these nanovaccines exhibited potent immunogenicity in humanized mouse models, underscoring their translational potential as next‐generation self‐adjuvanting vaccines.

## Linked entities

- **Chemicals:** Pam3CSK4 (PubChem CID 130704)
- **Diseases:** cancer (MONDO:0004992)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Diseases:** Cancer (MESH:D009369)
- **Chemicals:** lipid (MESH:D008055), Pam3CSK4 (-)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12970494/full.md

## References

83 references — full list in the complete paper: https://tomesphere.com/paper/PMC12970494/full.md

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Source: https://tomesphere.com/paper/PMC12970494