Advanced Materials

Peptide‐Oligonucleotide Nanohybrids Designed for Precise Gene Therapy of Rheumatoid Arthritis

Qing Wang 1
Xiaole Peng 1, 2
Xiaoting Gao 3
Yi Qin 1
Wenhao Li 1
Zebin Wu 1
Zhiqi Lao 3
Ang Gao 3
Ziyan Mao 4
Yaozeng Xu 1
Paul K. Chu 5
Xin Zhao 6
Dechun Geng 1
Huai-Yu Wang 3, 7, 8
Show full list: 14 authors
1
 
Department of Orthopedics The First Affiliated Hospital of Soochow University Suzhou Jiangsu 215006 China
2
 
Department of Orthopaedics The First Affiliated Hospital of Chongqing Medical University Chongqing 400016 China
3
 
Center for Human Tissues and Organs Degeneration Shenzhen Institute of Advanced Technology Chinese Academy of Sciences Shenzhen 518055 China
4
 
United World College of the Atlantic St Donat's Castle Vale of Glamorgan Llantwit Major CF61 1WF UK
7
 
Key Laboratory of Biomedical Imaging Science and System Chinese Academy of Sciences Shenzhen 518055 China
8
 
State Key Laboratory of Biomedical Imaging Science and System Shenzhen 518055 China
Publication typeJournal Article
Publication date2025-03-19
scimago Q1
wos Q1
SJR9.191
CiteScore43.0
Impact factor27.4
ISSN09359648, 15214095
Abstract

Rheumatoid arthritis (RA) is a chronic autoimmune disease characterized by excessive inflammation, pathological bone resorption, and systemic osteoporosis. It lacks effective treatment due to the complex pathogenesis. Gene therapy, especially targeted oligonucleotide (ON) delivery therapy, offers a new prospect for the precise treatment of RA. Nevertheless, the clinical application of ON delivery therapy still faces various challenges such as the rapid enzymolysis by RNAse, the lack of tissue targeting ability, difficulty in cell membrane penetration, and the incapability of endolysosomal escape. To address these issues, a novel kind of engineered peptide and oligonucleotide (PON) nanohybrids are designed and fabricated, which provide various advantages including good biosafety, inflammatory region‐targeted delivery, cell membrane penetration, reactive oxygen species (ROS) scavenging, and endolysosomal escape. The PON nanohybrids produce promising effects in suppressing inflammatory responses and osteoclastogenesis of macrophages via multiple signaling pathways. In vivo administration of PON nanohybrids not only ameliorates local joint bone destruction and systemic osteoporosis in the pathological state, but also demonstrates good prophylactic effects against the rapid progression of RA disease. In conclusion, the study presents a promising strategy for precise RA treatment and broadens the biomedical applications of gene therapy based on delivery system.

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