Manganese‐Coordinated Polyvalent Aptameric System (COMPASS) Enables DC‐Targeted mRNA/Mn <sup>2</sup> <sup>+</sup> Co‐Delivery for Cancer Immunotherapy

X Xueliang Liu (Punan Branch of Renji Hospital and Institute of Molecular Medicine (IMM) Renji Hospital School of Medicine Shanghai Jiao Tong University Shanghai 200125 P.R. China) Y Yuqing Li (Institute of High Energy Physics (IHEP)) X Xinfeng Dai (Punan Branch of Renji Hospital and Institute of Molecular Medicine (IMM) Renji Hospital School of Medicine Shanghai Jiao Tong University Shanghai 200125 P.R. China) Z Zhicheng Huang J Jiabei Li C Chuhuang Dong (Punan Branch of Renji Hospital and Institute of Molecular Medicine (IMM) Renji Hospital School of Medicine Shanghai Jiao Tong University Shanghai 200125 P.R. China) Z Ziliang Dong (Institute of Functional Nano &amp; Soft Materials (FUNSOM) Soochow University Suzhou 215123 China) D Dali Wei H Huayuan Zhou (Punan Branch of Renji Hospital and Institute of Molecular Medicine (IMM) Renji Hospital School of Medicine Shanghai Jiao Tong University Shanghai 200125 P.R. China) Z Zhuang Liu (Macao Institute of Materials Science and Engineering) Y Yu Yang W Weihong Tan (Institute of Molecular Medicine (IMM), Department of Nephrology, Molecular Cell Laboratory for Kidney Disease, Shanghai Peritoneal Dialysis Research Center, Uremia Diagnosis and Treatment Center, State Key Laboratory of Systems Medicine for Cancer, Renji Hospital, School of Medicine, School of Chemistry and Chemical Engineering)

Abstract

Abstract mRNA vaccines hold remarkable promise for cancer immunotherapy, yet current nanoparticle systems face challenges in efficacy, dendritic cell (DC) targeting, and safety. Herein, we report a nanoplatform, Manganese‐Coordinated Polyvalent Aptameric System (COMPASS), enabling targeted co‐delivery of mRNA and Mn 2 + to lymph node dendritic cells (DC) to boost potent antitumor immunity. The COMPASS employed rolling circle amplification to generate single‐stranded DNA scaffolds with multivalent DC‐targeting aptamers and polyT domains, enabling stable mRNA hybridization via A‐T pairing. Various metal ions were screened, and Mn 2 + was found to enhance mRNA endosomal escape and activate the STING pathway in DCs, promoting their maturation and antigen presentation. Controlled nanoparticle size (∼200 nm) and aptamer‐mediated DC targeting markedly enhanced lymphatic accumulation. In vivo evaluations revealed that COMPASS achieved potent prophylactic and therapeutic antitumor efficacy comparable to commercial LNPs (e.g., SM‐102), while exhibiting significantly enhanced safety profiles. Importantly, lyophilized COMPASS formulations retained their structural integrity and bioactivity for at least three months at room temperature. Overall, COMPASS represents a promising next‐generation nanoplatform with significant translational potential for safe and effective cancer immunotherapy.

Article Details

Volume / Issue Vol. 65, Issue 8
Published February 16, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (12)

X

Xueliang Liu

Punan Branch of Renji Hospital and Institute of Molecular Medicine (IMM) Renji Hospital School of Medicine Shanghai Jiao Tong University Shanghai 200125 P.R. China

Y

Yuqing Li

Institute of High Energy Physics (IHEP)

X

Xinfeng Dai

Punan Branch of Renji Hospital and Institute of Molecular Medicine (IMM) Renji Hospital School of Medicine Shanghai Jiao Tong University Shanghai 200125 P.R. China

Z

Zhicheng Huang

J

Jiabei Li

C

Chuhuang Dong

Punan Branch of Renji Hospital and Institute of Molecular Medicine (IMM) Renji Hospital School of Medicine Shanghai Jiao Tong University Shanghai 200125 P.R. China

Z

Ziliang Dong

Institute of Functional Nano &amp; Soft Materials (FUNSOM) Soochow University Suzhou 215123 China

D

Dali Wei

H

Huayuan Zhou

Punan Branch of Renji Hospital and Institute of Molecular Medicine (IMM) Renji Hospital School of Medicine Shanghai Jiao Tong University Shanghai 200125 P.R. China

Z

Zhuang Liu

Macao Institute of Materials Science and Engineering

Y

Yu Yang

W

Weihong Tan

Institute of Molecular Medicine (IMM), Department of Nephrology, Molecular Cell Laboratory for Kidney Disease, Shanghai Peritoneal Dialysis Research Center, Uremia Diagnosis and Treatment Center, State Key Laboratory of Systems Medicine for Cancer, Renji Hospital, School of Medicine, School of Chemistry and Chemical Engineering