| Literature DB >> 26171764 |
Karlo Perica, Joan Glick Bieler, Christian Schütz, Juan Carlos Varela, Jacqueline Douglass1, Andrew Skora1, Yen Ling Chiu, Mathias Oelke, Kenneth Kinzler1, Shibin Zhou1, Bert Vogelstein1, Jonathan P Schneck.
Abstract
Adoptive immunotherapy (AIT) can mediate durable regression of cancer, but widespread adoption of AIT is limited by the cost and complexity of generating tumor-specific T cells. Here we develop an Enrichment + Expansion strategy using paramagnetic, nanoscale artificial antigen presenting cells (aAPC) to rapidly expand tumor-specific T cells from rare naïve precursors and predicted neo-epitope responses. Nano-aAPC are capable of enriching rare tumor-specific T cells in a magnetic column and subsequently activating them to induce proliferation. Enrichment + Expansion resulted in greater than 1000-fold expansion of both mouse and human tumor-specific T cells in 1 week, with nano-aAPC based enrichment conferring a proliferation advantage during both in vitro culture and after adoptive transfer in vivo. Robust T cell responses were seen not only for shared tumor antigens, but also for computationally predicted neo-epitopes. Streamlining the rapid generation of large numbers of tumor-specific T cells in a cost-effective fashion through Enrichment + Expansion can be a powerful tool for immunotherapy.Entities:
Keywords: adoptive immunotherapy; immunotherapy; nanoparticles
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Year: 2015 PMID: 26171764 PMCID: PMC5082131 DOI: 10.1021/acsnano.5b02829
Source DB: PubMed Journal: ACS Nano ISSN: 1936-0851 Impact factor: 15.881