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一种用于在小鼠模型中激活免疫并对动脉粥样硬化进行预防性保护的纳米疫苗。

A nanovaccine for immune activation and prophylactic protection of atherosclerosis in mouse models.

作者信息

Zhang Lei, Al-Ammari Abdulrahman, Zhu Danxuan, Zhang Hongsong, Zhou Peng, Zhi Xu, Ding Weixiao, Li Xinmeng, Yu Qingqing, Gai Yuwen, Ma Xiaoling, Chen Chuntao, Zuo Chao, Zhang Jiaan, Zhu Wanying, Sun Dongping

机构信息

Chemicobiology and Functional Materials Institute, School of Chemistry and Chemical Engineering, Nanjing University of Science and Technology, Nanjing, PR China.

School of Chemistry and Materials Science, University of Science and Technology of China, Hefei, PR China.

出版信息

Nat Commun. 2025 Mar 2;16(1):2111. doi: 10.1038/s41467-025-57467-5.


DOI:10.1038/s41467-025-57467-5
PMID:40025093
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11873251/
Abstract

Vaccines offer prophylactic treatments against atherosclerosis by eliciting effector T cell and antibody responses, which require effective delivery of antigen and adjuvant to activate dendritic cells (DC). Here we show that individual conjugation of antigen p210 and adjuvant CpG oligodeoxynucleotides onto superparamagnetic iron oxide nanoparticles formulates a nanovaccine cocktail that activates DCs for antigen cross-presentation and induction of co-stimulatory signals, cytokines and CD8 effector/effector memory T cell responses. This nanovaccine modulates the DCs in the draining lymph nodes, activates both CD4 and CD8 T cells, elicits memory responses, and induces both anti-p210 IgM and IgG antibodies to suppress atherosclerosis. Lastly, three intradermal vaccinations of this nanovaccine mitigate the atherosclerosis development in the ApoE mice. Our nanovaccine design and preclinical data thus presents a potential candidate for prophylactic treatment for atherosclerosis.

摘要

疫苗通过引发效应T细胞和抗体反应提供针对动脉粥样硬化的预防性治疗,这需要有效地递送抗原和佐剂以激活树突状细胞(DC)。在这里,我们表明将抗原p210和佐剂CpG寡脱氧核苷酸分别偶联到超顺磁性氧化铁纳米颗粒上,可制成一种纳米疫苗混合物,该混合物可激活DC进行抗原交叉呈递并诱导共刺激信号、细胞因子和CD8效应/效应记忆T细胞反应。这种纳米疫苗可调节引流淋巴结中的DC,激活CD4和CD8 T细胞,引发记忆反应,并诱导抗p210 IgM和IgG抗体以抑制动脉粥样硬化。最后,对这种纳米疫苗进行三次皮内接种可减轻ApoE小鼠的动脉粥样硬化发展。因此,我们的纳米疫苗设计和临床前数据为动脉粥样硬化的预防性治疗提供了一个潜在的候选方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03fc/11873251/dfe1cc755c1c/41467_2025_57467_Fig10_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03fc/11873251/b75a0c4f3a74/41467_2025_57467_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03fc/11873251/1ff96f94917a/41467_2025_57467_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03fc/11873251/65e579bd9cff/41467_2025_57467_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03fc/11873251/f88ab45563f1/41467_2025_57467_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03fc/11873251/0fbf5f2ecf47/41467_2025_57467_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03fc/11873251/830db5af5c7d/41467_2025_57467_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03fc/11873251/e60e1b6ddcaf/41467_2025_57467_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03fc/11873251/adfc65a61fac/41467_2025_57467_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03fc/11873251/204b04a03c62/41467_2025_57467_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03fc/11873251/dfe1cc755c1c/41467_2025_57467_Fig10_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03fc/11873251/b75a0c4f3a74/41467_2025_57467_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03fc/11873251/1ff96f94917a/41467_2025_57467_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03fc/11873251/65e579bd9cff/41467_2025_57467_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03fc/11873251/f88ab45563f1/41467_2025_57467_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03fc/11873251/0fbf5f2ecf47/41467_2025_57467_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03fc/11873251/830db5af5c7d/41467_2025_57467_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03fc/11873251/e60e1b6ddcaf/41467_2025_57467_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03fc/11873251/adfc65a61fac/41467_2025_57467_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03fc/11873251/204b04a03c62/41467_2025_57467_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03fc/11873251/dfe1cc755c1c/41467_2025_57467_Fig10_HTML.jpg

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[1]
A nanovaccine for immune activation and prophylactic protection of atherosclerosis in mouse models.

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[4]
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[5]
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[6]
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[7]
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[8]
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[9]
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[10]
CD11c(+) dendritic cells maintain antigen processing, presentation capabilities, and CD4(+) T-cell priming efficacy under hypercholesterolemic conditions associated with atherosclerosis.

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本文引用的文献

[1]
Cellular and molecular waypoints along the path of T cell exhaustion.

Sci Immunol. 2023-9

[2]
Immunization using ApoB-100 peptide-linked nanoparticles reduces atherosclerosis.

JCI Insight. 2022-6-8

[3]
Two-Pronged Intracellular Co-Delivery of Antigen and Adjuvant for Synergistic Cancer Immunotherapy.

Adv Mater. 2022-5

[4]
The Mannose Receptor: From Endocytic Receptor and Biomarker to Regulator of (Meta)Inflammation.

Front Immunol. 2021

[5]
Antibodies against apoB100 peptide 210 inhibit atherosclerosis in apoE mice.

Sci Rep. 2021-4-27

[6]
Targeting Lysosomal Degradation Pathways: New Strategies and Techniques for Drug Discovery.

J Med Chem. 2021-4-8

[7]
Iron nanoparticles as novel vaccine adjuvants.

Eur J Pharm Sci. 2021-4-1

[8]
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Cells. 2020-11-30

[9]
Retinoic Acid-Loaded Poly(lactic--glycolic acid) Nanoparticle Formulation of ApoB-100-Derived Peptide 210 Attenuates Atherosclerosis.

J Biomed Nanotechnol. 2020-4-1

[10]
A DNA nanodevice-based vaccine for cancer immunotherapy.

Nat Mater. 2021-3

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