Active anti-cancer immune responses depend on efficient presentation of tumor antigens and co-stimulatory signals by antigen-presenting cells (APCs). Therapy with autologous natural APCs is costly and time-consuming and results in variable outcomes in clinical trials. Therefore, development of artificial APCs (aAPCs) has attracted significant interest as an alternative. We discuss the characteristics of various types of acellular aAPCs, and their clinical potential in cancer immunotherapy. The size, shape, and ligand mobility of aAPCs and their presentation of different immunological signals can all have significant effects on cytotoxic T cell activation. Novel optimized aAPCs, combining carefully tuned properties, may lead to efficient immunomodulation and improved clinical responses in cancer immunotherapy.
机构:
Harvard Univ, John A Paulson Sch Engn & Appl Sci, Cambridge, MA 02138 USA
Harvard Univ, Wyss Inst Biol Inspired Engn, Cambridge, MA 02138 USAHarvard Univ, John A Paulson Sch Engn & Appl Sci, Cambridge, MA 02138 USA
Cheung, Alexander S.
Zhang, David K. Y.
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机构:
Harvard Univ, John A Paulson Sch Engn & Appl Sci, Cambridge, MA 02138 USA
Harvard Univ, Wyss Inst Biol Inspired Engn, Cambridge, MA 02138 USAHarvard Univ, John A Paulson Sch Engn & Appl Sci, Cambridge, MA 02138 USA
Zhang, David K. Y.
Koshy, Sandeep T.
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机构:
Harvard Univ, John A Paulson Sch Engn & Appl Sci, Cambridge, MA 02138 USA
Harvard Univ, Wyss Inst Biol Inspired Engn, Cambridge, MA 02138 USA
Harvard MIT Div Hlth Sci & Technol, Cambridge, MA USAHarvard Univ, John A Paulson Sch Engn & Appl Sci, Cambridge, MA 02138 USA