| Literature DB >> 29441705 |
Ting-Yu Shih1,2, Serena O Blacklow1, Aileen W Li1,2, Benjamin R Freedman1,2, Sidi Bencherif1,2,3,4, Sandeep T Koshy1,2,5, Max C Darnell1,2, David J Mooney1,2.
Abstract
A covalently crosslinked methacrylated (MA)-alginate cryogel vaccine has been previously shown to generate a potent response against murine melanoma, but is not mechanically robust and requires a large 16G needle for delivery. Here, covalent and ionic crosslinking of cryogels are combined with the hypothesis that this will result in a tough MA-alginate cryogel with improved injectability. All tough cryogels can be injected through a smaller, 18G needle without sustaining any damage, while covalently crosslinked-only cryogels break after injection. Cytosine-phosphodiester-guanine (CpG)-delivering tough cryogels effectively activate dendritic cells (DCs). Granulocyte macrophage colony-stimulating factor releasing tough cryogels recruit four times more DCs than blank gels by day 7 in vivo. The tough cryogel vaccine induces strong antigen-specific cytotoxic T-lymphocyte and humoral responses. These vaccines prevent tumor formation in 80% of mice inoculated with HER2/neu-overexpressing DD breast cancer cells. The MA-alginate tough cryogels provide a promising minimally invasive delivery platform for cancer vaccinations.Entities:
Keywords: alginate; cancer vaccines; injectable; tough cryogels
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Year: 2018 PMID: 29441705 PMCID: PMC6467206 DOI: 10.1002/adhm.201701469
Source DB: PubMed Journal: Adv Healthc Mater ISSN: 2192-2640 Impact factor: 9.933