A Therapeutic Nanovaccine that Generates Anti‐Amyloid Antibodies and Amyloid‐specific Regulatory T Cells for Alzheimer's Disease. Issue 3 (19th December 2022)
- Record Type:
- Journal Article
- Title:
- A Therapeutic Nanovaccine that Generates Anti‐Amyloid Antibodies and Amyloid‐specific Regulatory T Cells for Alzheimer's Disease. Issue 3 (19th December 2022)
- Main Title:
- A Therapeutic Nanovaccine that Generates Anti‐Amyloid Antibodies and Amyloid‐specific Regulatory T Cells for Alzheimer's Disease
- Authors:
- Jung, Mungyo
Lee, Songmin
Park, Sohui
Hong, Jihye
Kim, Cheesue
Cho, Illhwan
Sohn, Hee Su
Kim, Kyunghwan
Park, In Wook
Yoon, Soljee
Kwon, Sungpil
Shin, Jisu
Lee, Donghee
Kang, Mikyung
Go, Seokhyung
Moon, Sangjun
Chung, Yeonseok
Kim, YoungSoo
Kim, Byung‐Soo - Abstract:
- Abstract: Alzheimer's disease (AD), the most common cause of dementia, is a complex condition characterized by multiple pathophysiological mechanisms including amyloid‐β (Aβ) plaque accumulation and neuroinflammation in the brain. The current immunotherapy approaches, such as anti‐Aβ monoclonal antibody (mAb) therapy, Aβ vaccines, and adoptive regulatory T (Treg) cell transfer, target a single pathophysiological mechanism, which may lead to unsatisfactory therapeutic efficacy. Furthermore, Aβ vaccines often induce T helper 1 (Th1) cell‐mediated inflammatory responses. Here, a nanovaccine composed of lipid nanoparticles loaded with Aβ peptides and rapamycin is developed, which targets multiple pathophysiological mechanisms, exhibits the combined effects of anti‐Aβ antibody therapy and adoptive Aβ‐specific Treg cell transfer, and can overcome the limitations of current immunotherapy approaches for AD. The Nanovaccine effectively delivers rapamycin and Aβ peptides to dendritic cells, produces both anti‐Aβ antibodies and Aβ‐specific Treg cells, removes Aβ plaques in the brain, alleviates neuroinflammation, prevents Th1 cell‐mediated excessive immune responses, and inhibits cognitive impairment in mice. The nanovaccine shows higher efficacy in cognitive recovery than an Aβ vaccine. Unlike anti‐Aβ mAb therapy and adoptive Treg cell transfer, both of which require complicated and costly manufacturing processes, the nanovaccine is easy‐to‐prepare and cost‐effective. The nanovaccinesAbstract: Alzheimer's disease (AD), the most common cause of dementia, is a complex condition characterized by multiple pathophysiological mechanisms including amyloid‐β (Aβ) plaque accumulation and neuroinflammation in the brain. The current immunotherapy approaches, such as anti‐Aβ monoclonal antibody (mAb) therapy, Aβ vaccines, and adoptive regulatory T (Treg) cell transfer, target a single pathophysiological mechanism, which may lead to unsatisfactory therapeutic efficacy. Furthermore, Aβ vaccines often induce T helper 1 (Th1) cell‐mediated inflammatory responses. Here, a nanovaccine composed of lipid nanoparticles loaded with Aβ peptides and rapamycin is developed, which targets multiple pathophysiological mechanisms, exhibits the combined effects of anti‐Aβ antibody therapy and adoptive Aβ‐specific Treg cell transfer, and can overcome the limitations of current immunotherapy approaches for AD. The Nanovaccine effectively delivers rapamycin and Aβ peptides to dendritic cells, produces both anti‐Aβ antibodies and Aβ‐specific Treg cells, removes Aβ plaques in the brain, alleviates neuroinflammation, prevents Th1 cell‐mediated excessive immune responses, and inhibits cognitive impairment in mice. The nanovaccine shows higher efficacy in cognitive recovery than an Aβ vaccine. Unlike anti‐Aβ mAb therapy and adoptive Treg cell transfer, both of which require complicated and costly manufacturing processes, the nanovaccine is easy‐to‐prepare and cost‐effective. The nanovaccines can represent a novel treatment option for AD. Abstract : Rapamycin‐incorporated lipid nanoparticle containing amyloid‐β (LNP‐R/Aβ) attenuates neuroinflammation and improves cognitive function in a transgenic rodent model of Alzheimer's disease (AD) by inducing tolerogenic dendritic cells and Aβ‐specific regulatory T cells, and generating anti‐amyloid antibodies. Furthermore, LNP‐R/Aβ reduces T helper 1 cells in AD brains, implying lower risks of meningitis, which is the major reason for the failure of conventional Aβ vaccines. … (more)
- Is Part Of:
- Advanced materials. Volume 35:Issue 3(2023)
- Journal:
- Advanced materials
- Issue:
- Volume 35:Issue 3(2023)
- Issue Display:
- Volume 35, Issue 3 (2023)
- Year:
- 2023
- Volume:
- 35
- Issue:
- 3
- Issue Sort Value:
- 2023-0035-0003-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2022-12-19
- Subjects:
- Alzheimer's disease -- anti‐amyloid antibodies -- antigen‐specific regulatory T cells -- lipid nanoparticles -- nanovaccines
Materials -- Periodicals
Chemical vapor deposition -- Periodicals
620.11 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-4095 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/adma.202207719 ↗
- Languages:
- English
- ISSNs:
- 0935-9648
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0696.897800
British Library DSC - BLDSS-3PM
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- 25163.xml