| Literature DB >> 28150213 |
Alyssa L Siefert1, Tarek M Fahmy1, Dongin Kim2,3.
Abstract
Artificial antigen-presenting cells (aAPCs) overcome many of the limitations of biologically based adoptive immunotherapy protocols. While these acellular systems can be designed with a variety of parameters, including material type, diameter, and proliferative signals for T cells, we outline methods to formulate and characterize a comprehensive polymeric microparticle aAPC platform. These aAPCs, which can be reproducibly fabricated in large quantities, efficiently stimulate antigen-specific T cell activation and proliferation by both paracrine cytokine signals and engagement of T cell surface proteins.Entities:
Keywords: Immunotherapy; Microparticle; PLGA; Paracrine delivery; Polymer; aAPC
Mesh:
Substances:
Year: 2017 PMID: 28150213 DOI: 10.1007/978-1-4939-6646-2_21
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745