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Smart Nanosized Drug Delivery Systems Inducing Immunogenic Cell Death for Combination with Cancer Immunotherapy
Lei Zhou1,2, Pengcheng Zhang1,3, Hao Wang2
1State Key Laboratory of Drug Research & Center of Pharmaceutics, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai 201203, China.
Abstract:
Cancer immunotherapy, which suppresses tumor relapse and metastasis by boosting host immunity and inducing long-term immune memory effects, is emerging as a vital approach to improve the prognosis of patients. Although remarkable efficacy has been observed in some patients, challenges including low response rate, drug resistance, and immune-related adverse effects still limit the clinical application of cancer immunotherapy in broad types of tumors. Immunotherapeutic agents are used to enhance tumor immunogenicity and reverse the effects of the immunosuppressive tumor microenvironment (ITM), but the benefits of monotherapy are mild and transient due to off-target distribution of drugs. To overcome these issues, smart nanosized drug delivery systems (sNDDS) have been developed to enhance tissue specificity, co-deliver multiple drugs, prime immune cells, and amplify immune responses in tumors. Moreover, accumulating knowledge in cancer biology, immunology, and material science has also greatly promoted the development of sNDDS for enhancing cancer immunotherapy.In this Account, we will discuss the approaches of our group in designing sNDDS to induce immunogenic cell death (ICD) for combination with cancer immunotherapy. We propose a brief overview on the design of nanocarriers, intelligent moieties and immunotherapeutic agents in sNDDS. Then, we discuss the strategies to remodel ITM by leveraging ICD as well as cooperating with programmed cell death protein 1 ligand blockade and indoleamine 2,3-dioxygenase 1 inhibition. We have synthesized a series of stimuli-responsive polymers and prodrugs to fabricate sNDDS and have integrated multiple immunotherapeutic drugs into one platform for combinational immunotherapy. Last, we present an outlook on future design of sNDDS and possible directions for enhancing cancer immunotherapy. Building on the concept of enhancing tumor immunogenicity and reversing ITM, we hope this Account will contribute to the rational design of sNDDS for co-delivery of multiple drugs with amplified immunotherapeutic efficacy.
Insights
Smart nanosized drug delivery systems (sNDDS) enhance cancer immunotherapy by inducing immunogenic cell death (ICD) and remodeling the tumor microenvironment. This approach overcomes limitations of monotherapy, improving treatment efficacy and patient prognosis.
Area of Science:
- Oncology
- Immunology
- Materials Science
- Nanotechnology
Background:
- Cancer immunotherapy shows promise but faces challenges like low response rates and drug resistance.
- Current immunotherapies often have mild, transient effects due to off-target drug distribution and immunosuppressive tumor microenvironments (ITM).
- Smart nanosized drug delivery systems (sNDDS) offer potential to improve specificity, co-deliver drugs, and amplify immune responses.
Purpose of the Study:
- To discuss the design of sNDDS for inducing immunogenic cell death (ICD) to enhance cancer immunotherapy.
- To explore strategies for remodeling the ITM using ICD in combination with other immunotherapies.
- To present an outlook on future sNDDS designs for improved cancer treatment.
Main Methods:
- Design of nanocarriers, intelligent moieties, and immunotherapeutic agents within sNDDS.
- Leveraging ICD to remodel the ITM, combined with programmed cell death protein 1 ligand blockade and indoleamine 2,3-dioxygenase 1 inhibition.
- Synthesis of stimuli-responsive polymers and prodrugs to fabricate sNDDS for multi-drug delivery.
Main Results:
- Development of sNDDS capable of co-delivering multiple immunotherapeutic drugs.
- Demonstration of strategies to enhance tumor immunogenicity and reverse ITM.
- Fabrication of integrated platforms for combinational immunotherapy using novel materials.
Conclusions:
- sNDDS can be rationally designed to induce ICD and remodel the ITM for enhanced cancer immunotherapy.
- Co-delivery of multiple drugs via sNDDS amplifies therapeutic efficacy compared to monotherapy.
- Future development of sNDDS holds significant potential for improving cancer treatment outcomes.
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