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本文引用的文献

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Alpha-alumina nanoparticles induce efficient autophagy-dependent cross-presentation and potent antitumour response.α-氧化铝纳米颗粒诱导有效的自噬依赖性交叉呈递和有效的抗肿瘤反应。
Nat Nanotechnol. 2011 Sep 18;6(10):645-50. doi: 10.1038/nnano.2011.153.
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A multifunctional core-shell nanoparticle for dendritic cell-based cancer immunotherapy.一种基于树突状细胞的癌症免疫治疗多功能核壳纳米颗粒。
Nat Nanotechnol. 2011 Sep 11;6(10):675-82. doi: 10.1038/nnano.2011.149.
3
Inhibitory Fcγ receptor engagement drives adjuvant and anti-tumor activities of agonistic CD40 antibodies.激动型 CD40 抗体通过抑制性 Fcγ 受体结合发挥佐剂和抗肿瘤活性。
Science. 2011 Aug 19;333(6045):1030-4. doi: 10.1126/science.1206954.
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Chimeric antigen receptor-modified T cells in chronic lymphoid leukemia.嵌合抗原受体修饰的 T 细胞治疗慢性淋巴细胞白血病。
N Engl J Med. 2011 Aug 25;365(8):725-33. doi: 10.1056/NEJMoa1103849. Epub 2011 Aug 10.
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Induction of potent anti-tumor responses while eliminating systemic side effects via liposome-anchored combinatorial immunotherapy.通过脂质体锚定的组合免疫疗法诱导有效的抗肿瘤反应,同时消除全身副作用。
Biomaterials. 2011 Aug;32(22):5134-47. doi: 10.1016/j.biomaterials.2011.03.067. Epub 2011 Apr 22.
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The targeted delivery of multicomponent cargos to cancer cells by nanoporous particle-supported lipid bilayers.纳米孔粒子支撑的脂质双层靶向递送至癌细胞的多组份 cargos。
Nat Mater. 2011 May;10(5):389-97. doi: 10.1038/nmat2992. Epub 2011 Apr 17.
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Porous silicon nanoparticle photosensitizers for singlet oxygen and their phototoxicity against cancer cells.多孔硅纳米粒子光敏剂用于单线态氧及其对癌细胞的光毒性。
ACS Nano. 2011 May 24;5(5):3651-9. doi: 10.1021/nn1035262. Epub 2011 Apr 6.
8
CD40 agonists alter tumor stroma and show efficacy against pancreatic carcinoma in mice and humans.CD40 激动剂可改变肿瘤基质,并在小鼠和人类中显示出对胰腺癌的疗效。
Science. 2011 Mar 25;331(6024):1612-6. doi: 10.1126/science.1198443.
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Interbilayer-crosslinked multilamellar vesicles as synthetic vaccines for potent humoral and cellular immune responses.层间交联的多层囊泡作为合成疫苗,引发强烈的体液和细胞免疫应答。
Nat Mater. 2011 Mar;10(3):243-51. doi: 10.1038/nmat2960. Epub 2011 Feb 20.
10
Designing vaccines based on biology of human dendritic cell subsets.基于人类树突状细胞亚群生物学设计疫苗。
Immunity. 2010 Oct 29;33(4):464-78. doi: 10.1016/j.immuni.2010.10.007.

多价多孔硅纳米粒子增强了激动型 CD40 抗体的免疫激活效力。

Multivalent porous silicon nanoparticles enhance the immune activation potency of agonistic CD40 antibody.

机构信息

Department of Chemistry and Biochemistry, University of California, San Diego, La Jolla, 92093-0358, USA.

出版信息

Adv Mater. 2012 Aug 2;24(29):3981-7. doi: 10.1002/adma.201200776. Epub 2012 Jun 12.

DOI:10.1002/adma.201200776
PMID:22689074
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3517000/
Abstract

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.

摘要

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。