Particle shape dependence of CD8+T cell activation by artificial antigen presenting cells

被引:205
|
作者
Sunshine, Joel C. [1 ,2 ]
Perica, Karlo [1 ,3 ,4 ]
Schneck, Jonathan P. [3 ,4 ,5 ,6 ]
Green, Jordan J. [1 ,2 ,5 ,7 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Biomed Engn, Baltimore, MD 21231 USA
[2] Johns Hopkins Univ, Sch Med, Translat Tissue Engn Ctr, Baltimore, MD 21231 USA
[3] Johns Hopkins Univ, Sch Med, Inst Cell Engn, Baltimore, MD 21231 USA
[4] Johns Hopkins Univ, Sch Med, Dept Pathol, Baltimore, MD 21231 USA
[5] Johns Hopkins Univ, Sch Med, Inst Nanobiotechnol, Baltimore, MD 21231 USA
[6] Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD 21231 USA
[7] Johns Hopkins Univ, Sch Med, Dept Ophthalmol, Baltimore, MD 21231 USA
关键词
Artificial antigen presenting cells; Particle shape; Ellipsoidal; Biomimetic; Microparticles; Immunotherapy; CYTOTOXIC T-CELLS; IMMUNOLOGICAL SYNAPSE; SURFACE; DESIGN; EXPANSION; DELIVERY; RECEPTOR; MEMORY; MODEL; NANOPARTICLES;
D O I
10.1016/j.biomaterials.2013.09.050
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Previous work developing particle-based acellular, artificial antigen presenting cells (aAPCs) has focused exclusively on spherical platforms. To explore the role of shape, we generated ellipsoidal PLGA microparticles with varying aspect ratios (ARs) and synthesized aAPCs from them. The ellipsoidal biomimetic aAPCs with high-AR showed significantly enhanced in vitro and in vivo activity above spherical aAPCs with particle volume and antigen content held constant. Confocal imaging indicates that CD8+ T cells preferentially migrate to and are activated by interaction with the long axis of the aAPC. Importantly, enhanced activity of high-AR aAPCs was seen in a mouse melanoma model, with high-AR aAPCs improving melanoma survival compared to non-cognate aAPCs (p = 0.004) and cognate spherical aAPCs (p = 0.05). These findings indicate that particle geometry is a critical design criterion in the generation of aAPCs, and may offer insight into the essential role of geometry in the interaction between CD8+ T cells and biological APCs. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:269 / 277
页数:9
相关论文
共 50 条
  • [41] Modulation of CD4+and CD8+T Cell Responses by Retinal-Antigen Specific Regulatory T Cells
    McPherson, S. W.
    Heuss, N. D.
    Gregerson, D. S.
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2010, 51 (13)
  • [42] CD8+T cells require signal 3 from non-antigen-presenting cells for optimal clonal expansion
    Abe, J.
    Germann, P.
    Ripoll, J.
    Sharpe, J.
    Stein, J. V.
    SWISS MEDICAL WEEKLY, 2023, 153 : 12S - 12S
  • [43] Artificial Antigen-Presenting Cell Topology Dictates T Cell Activation
    Wauters, Annelies C.
    Scheerstra, Jari F.
    Vermeijlen, Irma G.
    Hammink, Roel
    Schluck, Marjolein
    Woythe, Laura
    Wu, Hanglong
    Albertazzi, Lorenzo
    Figdor, Carl G.
    Tel, Jurjen
    Abdelmohsen, Loai K. E. A.
    van Hest, Jan C. M.
    ACS NANO, 2022, 16 (06) : 15072 - 15085
  • [44] Activation and expansion of human T cells using artificial antigen-presenting cell scaffolds
    David K. Y. Zhang
    Alexander S. Cheung
    David J. Mooney
    Nature Protocols, 2020, 15 : 773 - 798
  • [45] Fractionated Radiation Severely Reduces the Number of CD8+T Cells and Mature Antigen Presenting Cells Within Lung Tumors
    Reijmen, Eva
    De Mey, Sven
    De Mey, Wout
    Gevaert, Thierry
    De Ridder, Kirsten
    Locy, Hanne
    Martens, Sandrina
    De Blay, Emmy
    Bouwens, Luc
    Debie, Pieterjan
    Breckpot, Karine
    De Greve, Jacques
    De Ridder, Mark
    Goyvaerts, Cleo
    INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2021, 111 (01): : 272 - 283
  • [46] Activation and expansion of human T cells using artificial antigen-presenting cell scaffolds
    Zhang, David K. Y.
    Cheung, Alexander S.
    Mooney, David J.
    NATURE PROTOCOLS, 2020, 15 (03) : 773 - 798
  • [47] CD8+T cells require signal 3 from non-antigen-presenting cells for optimal clonal expansion
    Abe, Jun
    Germann, Philipp
    Ripoll, Jorge
    Sharpe, James
    Stein, Jens V.
    EUROPEAN JOURNAL OF IMMUNOLOGY, 2021, 51 : 46 - 46
  • [48] Artificial Antigen Presenting Cell (aAPC) Mediated Activation and Expansion of Natural Killer T Cells
    East, James E.
    Sun, Wenji
    Webb, Tonya J.
    JOVE-JOURNAL OF VISUALIZED EXPERIMENTS, 2012, (70):
  • [49] Nanoscale artificial antigen presenting cells for T cell immunotherapy
    Perica, Karlo
    Medero, Andres De Leon
    Durai, Malarvizhi
    Chiu, Yen Ling
    Bieler, Joan Glick
    Sibener, Leah
    Niemoeller, Michaela
    Assenmacher, Mario
    Richter, Anne
    Edidin, Michael
    Oelke, Mathias
    Schneck, Jonathan
    NANOMEDICINE-NANOTECHNOLOGY BIOLOGY AND MEDICINE, 2014, 10 (01) : 119 - 129
  • [50] Nanoscale Artificial Antigen Presenting Cells for T Cell immunotherapy
    Perica, Karlo
    Bieler, Joan G.
    Medero, Andres De Leon
    Chiu, Yen-Ling
    Durai, Malarvizhi
    Niemoeller, Michaele
    Assenmacher, Mario
    Richter, Anne
    Oelke, Mathias
    Schneck, Jonathan
    CANCER RESEARCH, 2013, 73 (08)