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Publication

Hitchhiking nanoparticles

Journal Contribution - Journal Article

Subtitle:Reversible coupling of lipid-based nanoparticles to cytotoxic T lymphocytes

Following intravenous injection of anti-cancer nanomedicines, many barriers need to be overcome en route to the tumor. Cell-mediated delivery of nanoparticles (NPs) is promising in terms of overcoming several of these barriers based on the tumoritropic migratory properties of particular cell types. This guided transport aims to enhance the NP accumulation in the tumor and moreover enhance the infiltration of regions that are typically inaccessible for free NPs. Within this study, cytotoxic CD8(+) T cells were selected as carriers based on both their ability to migrate to the tumor and their intrinsic cytolytic activity against tumor cells. Many anti-cancer nanomedicines require tumor cell internalization to mediate cytosolic drug delivery and enhance the anti-cancer effect. This proof-of-concept therefore reports on the reversible attachment of liposomes to the surface of cytotoxic T lymphocytes via a reduction sensitive coupling. The activation status of the T cells and the liposome composition are shown to strongly influence the loading efficiency. Loading the cells with liposomes does not compromise T cell functionalities like proliferation and cytolytic function. Additionally, the triggered liposome release is demonstrated upon the addition of glutathione. Based on this optimization using liposomes as model NPs, a small interfering RNA (siRNA)-loaded NP was developed that can be coupled to the surface of CD8(+) T cells.

Journal: Biomaterials
ISSN: 0142-9612
Volume: 77
Pages: 243-254
Number of pages: 12
Publication year:2016
Keywords:Animals, Cell Line, Tumor, Cell Movement, Cytotoxicity, Immunologic, Dextrans, Disulfides, Drug Delivery Systems, Extravasation of Diagnostic and Therapeutic Materials, Glutathione, Hydrogels, Immunotherapy, Adoptive, Liposomes, Lymphocyte Activation, Lymphocytes, Tumor-Infiltrating, Methacrylates, Mice, Nanoparticles, Ovalbumin, Phosphatidylcholines, Phosphatidylethanolamines, Phosphatidylglycerols, Pyridines, RNA, Small Interfering, Receptors, Antigen, T-Cell, T-Lymphocytes, Cytotoxic, Thymoma, Research Support, Non-U.S. Gov't