Department of Chemistry and Biochemistry, University of California, San Diego, La Jolla, 92093-0358, USA.
Adv Mater. 2012 Aug 2;24(29):3981-7. doi: 10.1002/adma.201200776. Epub 2012 Jun 12.
One of the fundamental paradigms in the use of nanoparticles to treat disease is to evade or suppress the immune system in order to minimize systemic side effects and deliver sufficient nanoparticle quantities to the intended tissues. However, the immune system is the body's most important and effective defense against diseases. It protects the host by identifying and eliminating foreign pathogens as well as self-malignancies. Here we report a nanoparticle engineered to work with the immune system, enhancing the intended activation of antigen presenting cells (APCs). We show that luminescent porous silicon nanoparticles (LPSiNPs), each containing multiple copies of an agonistic antibody (FGK45) to the APC receptor CD40, greatly enhance activation of B cells. The cellular response to the nanoparticle-based stimulators is equivalent to a 30-40 fold larger concentration of free FGK45. The intrinsic near-infrared photoluminescence of LPSiNPs is used to monitor degradation and track the nanoparticles inside APCs.
利用纳米粒子治疗疾病的基本范例之一是逃避或抑制免疫系统,以最大限度地减少全身副作用并将足够数量的纳米粒子递送到预期的组织中。然而,免疫系统是人体对抗疾病最重要和最有效的防御机制。它通过识别和消除外来病原体以及自身恶性肿瘤来保护宿主。在这里,我们报告了一种经过工程设计的与免疫系统协同作用的纳米粒子,增强了抗原呈递细胞 (APC) 的预期激活。我们表明,每个含有多个激动型抗体 (FGK45) 拷贝的发光多孔硅纳米粒子 (LPSiNPs) 可极大地增强 B 细胞的激活。基于纳米粒子的刺激物的细胞反应相当于游离 FGK45 浓度增加 30-40 倍。LPSiNPs 的固有近红外光致发光用于监测降解并跟踪 APC 内的纳米粒子。