Disrupting Complement‐Inflammation Positive Feedback Circuit via Oligonucleotide Hydrogel Microspheres for Reversing Joint Inflammation

Y Yu Zhang (Xiangya Hospital, Central South University Changsha China) W Wu Yang (State Key Laboratory of Systems Medicine for Cancer, Shanghai Cancer Institute, Renji Hospital, Shanghai Jiao Tong University School of Medicine) W Wei Xiong Y Yu Chen P Pengzhen Zhuang (Department of Orthopaedics Shanghai Key Laboratory for Prevention and Treatment of Bone and Joint Diseases Shanghai Institute of Traumatology and Orthopaedics Ruijin Hospital Shanghai Jiao Tong University School of Medicine 197 Ruijin 2nd Road Shanghai 200025 P. R. China) H Haoran Wang (New Cornerstone Science Laboratory, State Key Laboratory for Physical Chemistry of Solid Surfaces, Collaborative Innovation Center of Chemistry for Energy Materials, and National & Local Joint Engineering Research Center of Preparation Technology of Nanomaterials, College of Chemistry and Chemical Engineering) D Diana M. Toivola (Cell Biology Biosciences Faculty of Science and Engineering Åbo Akademi University Turku 20520 Finland) Y Yawei Du (School of Chemical Engineering and Technology Engineering Research Center of Seawater Utilization of Ministry of Education Hebei University of Technology Tianjin P. R. China) H Hongbo Zhang W Wenguo Cui

Abstract

Abstract The positive feedback circuit between the complement system and inflammatory immune responses maps the malignant progression of chronic joint inflammation. Prolonged dysregulation of the immune microenvironment in rheumatoid arthritis (RA) further exacerbates sustained complement activation, thereby establishing a vicious cycle. In this study, MMP‐9‐responsive, injectable micro‐nano geneplexes (C5ASO@HAP‐CL‐TIMP@HMs) are developed for on‐demand regulation of complement component C5, aiming to disrupt this pathological circuit. C5 antisense oligonucleotides (C5ASO) are loaded into cationic liposomes, which are subsequently encapsulated within hyaluronic acid microspheres via click chemistry. In vitro, these geneplexes effectively block abnormal C5 activation in RA synoviocytes, restore macrophage polarization balance, reduce pro‐inflammatory cytokine levels and immune complex precursor molecules, and upregulate anti‐inflammatory mediators. In an adjuvant‐induced arthritis rat model, they significantly alleviate joint swelling and cartilage degradation and suppress inflammatory responses, further highlighting the therapeutic potential of geneplexes in dismantling the complement‐inflammation circuit. In summary, the development of micro‐nano geneplexes capable of precisely disrupting the complement‐inflammatory circuit in RA offers a promising new perspective for the targeted treatment of chronic joint inflammation.

Article Details

Volume / Issue Vol. 38, Issue 8
Published February 01, 2026
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (10)

Y

Yu Zhang

Xiangya Hospital, Central South University Changsha China

W

Wu Yang

State Key Laboratory of Systems Medicine for Cancer, Shanghai Cancer Institute, Renji Hospital, Shanghai Jiao Tong University School of Medicine

W

Wei Xiong

Y

Yu Chen

P

Pengzhen Zhuang

Department of Orthopaedics Shanghai Key Laboratory for Prevention and Treatment of Bone and Joint Diseases Shanghai Institute of Traumatology and Orthopaedics Ruijin Hospital Shanghai Jiao Tong University School of Medicine 197 Ruijin 2nd Road Shanghai 200025 P. R. China

H

Haoran Wang

New Cornerstone Science Laboratory, State Key Laboratory for Physical Chemistry of Solid Surfaces, Collaborative Innovation Center of Chemistry for Energy Materials, and National & Local Joint Engineering Research Center of Preparation Technology of Nanomaterials, College of Chemistry and Chemical Engineering

D

Diana M. Toivola

Cell Biology Biosciences Faculty of Science and Engineering Åbo Akademi University Turku 20520 Finland

Y

Yawei Du

School of Chemical Engineering and Technology Engineering Research Center of Seawater Utilization of Ministry of Education Hebei University of Technology Tianjin P. R. China

H

Hongbo Zhang

W

Wenguo Cui