Oral administration of probiotic colony-like micro-nano system for immunoregulation of rheumatoid arthritis

Fangke Zhang(Shanghai Jiao Tong University), Tao Ding(Shanghai Jiao Tong University), Jiancheng Zheng(Shanghai Jiao Tong University), Nan Li(Second Affiliated Hospital of Guangzhou Medical University), Zhigang Li(Second Affiliated Hospital of Guangzhou Medical University), Xuefei Wang(Ruijin Hospital), Yawei Du(Shanghai Jiao Tong University), Weiguo Hu(Ruijin Hospital), Wenguo Cui(Shanghai Jiao Tong University), Weisheng Guo(Second Affiliated Hospital of Guangzhou Medical University)
Acta Pharmaceutica Sinica B
October 31, 2025
Cited by 1Open Access
Full Text

Abstract

Rheumatoid arthritis (RA) is a chronic systemic autoimmune disease that requires long-term pharmacological management. Melittin, a peptide derived from bee venom, has shown promising therapeutic efficacy for RA by modulating immune balance. Given the critical role of the gut in immune regulation, oral administration of melittin could have significant clinical implications. However, this approach faces substantial challenges, including degradation by gastric fluids and off-target adverse effects, which compromise its efficacy and safety. To address these limitations, we developed an innovative orally administered, gut-targeted micro-nano system (SPM/AlgL) inspired by bacterial colonies. Herein, gas-shearing microfluidics is leveraged to monodisperse sialic acid-decorated peptide nanomedicines within calcium alginate microgels. These microspheres are then coated with probiotic biofilms, leveraging their acid resistance and intestinal adhesion properties. The biofilm coating effectively protects melittin from gastric degradation and enhances its accumulation in the mesenteric lymph nodes, thereby improving its targeting ability to inflammatory sites and reducing adverse effects. By modulating the Th1/Th2 and Th17/Treg ratios in the mesenteric lymph nodes and spleen tissues, this system successfully alleviates immune responses and efficiently mitigates the progression of arthritis. Overall, this oral therapeutic strategy demonstrates significant potential for advancing the immunotherapy of RA and other systemic autoimmune diseases.


Related Papers

No related papers found

Powered by citation graph analysis