TY - JOUR
T1 - Emerging biomaterial-based strategies for personalized therapeutic in situ cancer vaccines
AU - Viswanath, Dixita Ishani
AU - Liu, Hsuan Chen
AU - Huston, David P.
AU - Chua, Corrine Ying Xuan
AU - Grattoni, Alessandro
N1 - Funding Information:
AG receives funding support from the Center for Immunotherapeutic Transport Oncophysics [grant number U54CA210181 , pilot award], Houston Methodist Research Institute , through the Department of Defense [grant number W81XWH-20-1-0600 ], Nancy Owens Breast Cancer Foundation , and Golfers Against Cancer . D.I.V. received joint funding support from Texas A&M University MD/PhD Program and Houston Methodist Research Institute . D.P.H. is supported in part by the National Institutes of Health [grant number R01AI097372 ] and the W. Bryan Trammell, Jr. Family Presidential Distinguished Chair in Allergy & Immunology.
Publisher Copyright:
© 2021 Elsevier Ltd
Copyright:
Copyright 2021 Elsevier B.V., All rights reserved.
PY - 2022/1
Y1 - 2022/1
N2 - Landmark successes in oncoimmunology have led to development of therapeutics boosting the host immune system to eradicate local and distant tumors with impactful tumor reduction in a subset of patients. However, current immunotherapy modalities often demonstrate limited success when involving immunologically cold tumors and solid tumors. Here, we describe the role of various biomaterials to formulate cancer vaccines as a form of cancer immunotherapy, seeking to utilize the host immune system to activate and expand tumor-specific T cells. Biomaterial-based cancer vaccines enhance the cancer-immunity cycle by harnessing cellular recruitment and activation against tumor-specific antigens. In this review, we discuss biomaterial-based vaccine strategies to induce lymphocytic responses necessary to mediate anti-tumor immunity. We focus on strategies that selectively attract dendritic cells via immunostimulatory gradients, activate them against presented tumor-specific antigens, and induce effective cross-presentation to T cells in secondary lymphoid organs, thereby generating immunity. We posit that personalized cancer vaccines are promising targets to generate long-term systemic immunity against patient- and tumor-specific antigens to ensure long-term cancer remission.
AB - Landmark successes in oncoimmunology have led to development of therapeutics boosting the host immune system to eradicate local and distant tumors with impactful tumor reduction in a subset of patients. However, current immunotherapy modalities often demonstrate limited success when involving immunologically cold tumors and solid tumors. Here, we describe the role of various biomaterials to formulate cancer vaccines as a form of cancer immunotherapy, seeking to utilize the host immune system to activate and expand tumor-specific T cells. Biomaterial-based cancer vaccines enhance the cancer-immunity cycle by harnessing cellular recruitment and activation against tumor-specific antigens. In this review, we discuss biomaterial-based vaccine strategies to induce lymphocytic responses necessary to mediate anti-tumor immunity. We focus on strategies that selectively attract dendritic cells via immunostimulatory gradients, activate them against presented tumor-specific antigens, and induce effective cross-presentation to T cells in secondary lymphoid organs, thereby generating immunity. We posit that personalized cancer vaccines are promising targets to generate long-term systemic immunity against patient- and tumor-specific antigens to ensure long-term cancer remission.
KW - Biomaterials
KW - Cancer vaccine
KW - In situ delivery
KW - Local controlled release
KW - Oncoimmunotherapy
KW - Biocompatible Materials/therapeutic use
KW - Humans
KW - Immunotherapy
KW - Cancer Vaccines/therapeutic use
KW - Neoplasms/drug therapy
KW - Antigens, Neoplasm/therapeutic use
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U2 - 10.1016/j.biomaterials.2021.121297
DO - 10.1016/j.biomaterials.2021.121297
M3 - Review article
C2 - 34902729
AN - SCOPUS:85120872487
SN - 0142-9612
VL - 280
SP - 121297
JO - Biomaterials
JF - Biomaterials
M1 - 121297
ER -