Shape matters: Biodegradable anisotropic nanoparticle artificial antigen presenting cells for cancer immunotherapy

被引:25
作者
Ben-Akiva, Elana [1 ,2 ,3 ]
Hickey, John W. [1 ,3 ,4 ,5 ]
Meyer, Randall A. [1 ,2 ,3 ]
Isser, Ariel [1 ,3 ,4 ,5 ]
Shannon, Sydney R. [1 ,2 ,3 ,4 ,5 ]
Livingston, Natalie K. [1 ,3 ,4 ,5 ]
Rhodes, Kelly R. [1 ,2 ,3 ]
Kosmides, Alyssa K. [1 ,3 ,4 ,5 ]
Warren, Tiarra R. [1 ,2 ,3 ]
Tzeng, Stephany Y. [1 ,2 ,3 ]
Schneck, Jonathan P. [3 ,4 ,5 ,6 ]
Green, Jordan J. [1 ,2 ,3 ,7 ,8 ,9 ,10 ,11 ]
机构
[1] Johns Hopkins Univ, Dept Biomed Engn, Sch Med, Baltimore, MD 21231 USA
[2] Johns Hopkins Univ, Translat Tissue Engn Ctr, Sch Med, Baltimore, MD 21231 USA
[3] Johns Hopkins Univ, Inst NanoBioTechnol, Sch Med, Baltimore, MD 21231 USA
[4] Johns Hopkins Univ, Inst Cell Engn, Sch Med, Baltimore, MD 21231 USA
[5] Johns Hopkins Univ, Dept Pathol, Sch Med, Baltimore, MD 21231 USA
[6] Johns Hopkins Univ, Dept Med, Sch Med, Baltimore, MD 21231 USA
[7] Johns Hopkins Univ, Dept Mat Sci & Engn, Baltimore, MD 21231 USA
[8] Johns Hopkins Univ, Dept Chem & Biomol Engn, Baltimore, MD 21231 USA
[9] Johns Hopkins Univ, Dept Ophthalmol, Sch Med, Baltimore, MD 21231 USA
[10] Johns Hopkins Univ, Sidney Kimmel Comprehens Canc Ctr, Dept Oncol, Sch Med, Baltimore, MD 21231 USA
[11] Johns Hopkins Univ, Bloomberg Kimmel Inst Canc Immunotherapy, Sch Med, Baltimore, MD 21231 USA
关键词
Artificial antigen presenting cell; Nanoparticle shape; Cancer; Immunoengineering; Biomimetic; CYTOTOXIC T-CELLS; ACTIVATION; COSTIMULATION; PARTICLES; INDUCTION; EXPANSION; IL-2;
D O I
10.1016/j.actbio.2023.02.023
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Artificial antigen presenting cells are biomimetic particles that recapitulate the signals presented by nat-ural antigen presenting cells in order to stimulate T cells in an antigen-specific manner using an acellular platform. We have engineered an enhanced nanoscale biodegradable artificial antigen presenting cell by modulating particle shape to achieve a nanoparticle geometry that allows for increased radius of curva-ture and surface area for T cell contact. The non-spherical nanoparticle artificial antigen presenting cells developed here have reduced nonspecific uptake and improved circulation time compared both to spher-ical nanoparticles and to traditional microparticle technologies. Additionally, the anisotropic nanoparti-cle artificial antigen presenting cells efficiently engage with and activate T cells, ultimately leading to a marked anti-tumor effect in a mouse melanoma model that their spherical counterparts were unable to achieve.Artificial antigen presenting cells (aAPC) can activate antigen-specific CD8 + T cells but have largely been limited to microparticle-based platforms and ex vivo T cell expansion. Although more amenable to in vivo use, nanoscale aAPC have traditionally been ineffective due to limited surface area available for T cell interaction. In this work, we engineered non-spherical biodegradable nanoscale aAPC to investigate the role of particle geometry and develop a translatable platform for T cell activation. The non-spherical aAPC developed here have increased surface area and a flatter surface for T cell engagement and, therefore, can more effectively stimulate antigen-specific T cells, resulting in anti-tumor efficacy in a mouse melanoma model.(c) 2023 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:187 / 197
页数:11
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