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Environment-responsive dendrobium polysaccharide hydrogel embedding manganese microsphere as a post-operative adjuvant to boost cascaded immune cycle against melanoma

Nan GaoSchool of Pharmacy, Guizhou Medical University, Guizhou 561113, ChinaYiran HuangNMPA Key Laboratory for Quality Research and Evaluation of Pharmaceutical Excipients, Shanghai 201203, ChinaShisuo JingZhongshan Institute for Drug Discovery, SIMM, CAS, Zhongshan 528400, ChinaMeng ZhangDepartment of Pharmacy, Women's Hospital, Zhejiang University School of Medicine, Hangzhou 310006, ChinaErgang LiuZhongshan Institute for Drug Discovery, SIMM, CAS, Zhongshan 528400, ChinaLu QiuArtemisinin Research Center, Guangzhou University of Chinese Medicine, Guangzhou 510450, ChinaJing‐Long HuangSchool of Pharmacy, Guizhou Medical University, Guizhou 561113, ChinaBahtiyor MuhitdinovInstitute of Bioorganic Chemistry, Uzbekistan Academy of Sciences, Tashkent 100125, UzbekistanYongzhuo HuangNMPA Key Laboratory for Quality Research and Evaluation of Pharmaceutical Excipients, Shanghai 201203, China
Theranosticsjournal2024en
ABI

Abstract

Rationale: Surgical resection is a primary treatment for solid tumors, but high rates of tumor recurrence and metastasis post-surgery present significant challenges.Manganese (Mn 2+ ), known to enhance dendritic cell-mediated cancer immunotherapy by activating the cGAS-STING pathway, has potential in post-operative cancer management.However, achieving prolonged and localized delivery of Mn 2+ to stimulate immune responses without systemic toxicity remains a challenge.Methods: We developed a post-operative microenvironment-responsive dendrobium polysaccharide hydrogel embedded with Mn 2+ -pectin microspheres (MnP@DOP-Gel).This hydrogel system releases Mn 2+ -pectin microspheres (MnP) in response to ROS, and MnP shows a dual effect in vitro: promoting immunogenic cell death and activating immune cells (dendritic cells and macrophages).The efficacy of MnP@DOP-Gel as a post-surgical treatment and its potential for immune activation were assessed in both subcutaneous and metastatic melanoma models in mice, exploring its synergistic effect with anti-PD1 antibody.Result: MnP@DOP-Gel exhibited ROS-responsive release of MnP, which could exert dual effects by inducing immunogenic cell death of tumor cells and activating dendritic cells and macrophages to initiate a cascade of anti-tumor immune responses.In vivo experiments showed that the implanted MnP@DOP-Gel significantly inhibited residual tumor growth and metastasis.Moreover, the combination of MnP@DOP-Gel and anti-PD1 antibody displayed superior therapeutic potency in preventing either metastasis or abscopal brain tumor growth.Conclusions: MnP@DOP-Gel represents a promising drug-free strategy for cancer post-operative management.Utilizing this Mn 2+ -embedding and ROS-responsive delivery system, it regulates surgery-induced immune responses and promotes sustained anti-tumor responses, potentially increasing the effectiveness of surgical cancer treatments.

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