4.8 Article

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

期刊

BIOMATERIALS
卷 35, 期 1, 页码 269-277

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.biomaterials.2013.09.050

关键词

Artificial antigen presenting cells; Particle shape; Ellipsoidal; Biomimetic; Microparticles; Immunotherapy

资金

  1. Johns Hopkins University Institute for Nanobiotechnology
  2. NIH [P01-AI072677, R01-EB016721, R01-AI44129, R01-CA108835]
  3. MSTP program
  4. Cancer Research Institute Predoctoral Fellowship
  5. NATIONAL CANCER INSTITUTE [R01CA108835] Funding Source: NIH RePORTER
  6. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [P01AI072677, R01AI044129] Funding Source: NIH RePORTER
  7. NATIONAL INSTITUTE OF BIOMEDICAL IMAGING AND BIOENGINEERING [R01EB016721] Funding Source: NIH RePORTER
  8. NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES [P30DK079637] Funding Source: NIH RePORTER
  9. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [T32GM007309] Funding Source: NIH RePORTER

向作者/读者索取更多资源

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.

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