Dual‐Antigen‐Displaying Nanovaccines Elicit Synergistic Immunoactivation for Treating Cancer and Preventing Infectious Complications

Author:

Chen Fangjie12,Zhang Mengmeng1,Yang Fengmin1,Wang Lu1ORCID,Liu Jinyao1ORCID,Liu Junqiu3,Pang Yan4

Affiliation:

1. Shanghai Key Laboratory for Nucleic Acid Chemistry and Nanomedicine Institute of Molecular Medicine State Key Laboratory of Systems Medicine for Cancer Renji Hospital School of Medicine Shanghai Jiao Tong University Shanghai 200127 China

2. Department of Oncology The First Affiliated Hospital of Shandong First Medical University & Shandong Provincial Qianfoshan Hospital Shandong Key Laboratory of Rheumatic Disease and Translational Medicine Shandong Lung Cancer Institute Jinan Shandong 250117 China

3. College of Material Chemistry and Chemical Engineering Key Laboratory of Organosilicon Chemistry and Material Technology Ministry of Education Key Laboratory of Organosilicon Material Technology Hangzhou Normal University Hangzhou Zhejiang 311121 China

4. Shanghai Key Laboratory of Orbital Diseases and Ocular Oncology Department of Ophthalmology Shanghai Ninth People's Hospital School of Medicine Shanghai Jiao Tong University Shanghai 200011 China

Abstract

AbstractAs one of the most common complications, infection causes the majority of mortality in cancer patients. However, therapeutic strategies that can simultaneously suppress tumors and protect patients from infection have been rarely reported. Here, the use of dual‐antigen‐displaying nanovaccines (DADNs) is described to elicit synergistic immunoactivation for treating cancer and preventing infectious complications. DADNs are prepared by wrapping immunoadjuvant‐loaded nanoparticles with a hybrid coating, which is fused from cell membranes that are separately genetically engineered to express tumor and infectious pathogenic antigens. Due to the presence of a dual‐antigen combination, DADNs are able to promote the maturation of dendritic cells and more importantly to trigger cross‐presentation of both combined antigens. During in vivo investigations, we find that DADNs can reverse immunosuppression by stimulating tumor‐associated antigen‐specific T‐cell responses, resulting in significantly delayed tumor growth in mice. These nanovaccines also elicit effective protective immunity against tumor challenges and induce robust production of pathogenic antigen‐specific immunoglobulin G antibody in a prophylactic study. This work offers a unique approach to develop dual‐mode vaccines, which are promising for synchronously treating cancer and preventing infection.

Funder

National Key Research and Development Program of China

Innovative Research Team of High-level Local University in Shanghai

Natural Science Foundation of Shandong Province

National Natural Science Foundation of China

Fundamental Research Funds for the Central Universities

Publisher

Wiley

Subject

Biomaterials,Biotechnology,General Materials Science,General Chemistry

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