Immunological Evaluation of Co‐Assembling a Lipidated Peptide Antigen and Lipophilic Adjuvants: Self‐Adjuvanting Anti‐Breast‐Cancer Vaccine Candidates. Issue 40 (11th August 2020)
- Record Type:
- Journal Article
- Title:
- Immunological Evaluation of Co‐Assembling a Lipidated Peptide Antigen and Lipophilic Adjuvants: Self‐Adjuvanting Anti‐Breast‐Cancer Vaccine Candidates. Issue 40 (11th August 2020)
- Main Title:
- Immunological Evaluation of Co‐Assembling a Lipidated Peptide Antigen and Lipophilic Adjuvants: Self‐Adjuvanting Anti‐Breast‐Cancer Vaccine Candidates
- Authors:
- Aiga, Taku
Manabe, Yoshiyuki
Ito, Keita
Chang, Tsung‐Che
Kabayama, Kazuya
Ohshima, Shino
Kametani, Yoshie
Miura, Ayane
Furukawa, Hiroto
Inaba, Hiroshi
Matsuura, Kazunori
Fukase, Koichi - Abstract:
- Abstract: Co‐assembling vaccines composed of a lipidated HER2‐derived antigenic CH401 peptide and either a lipophilic adjuvant, Pam3 CSK4, α‐GalCer, or lipid A 506, were evaluated as breast cancer vaccine candidates. This vaccine design was aimed to inherit both antigen multivalency and antigen‐specific immunostimulation properties, observed in reported self‐adjuvanting vaccine candidates, by using self‐assembly and adjuvant‐conjugated antigens. Under vaccination concentrations, respective lipophilic adjuvants underwent co‐assembly with lipidated CH401, which boosted the anti‐CH401 IgG and IgM production. In particular, α‐GalCer was responsible for the most significant immune activation. Therefore, the newly developed vaccine design enabled the optimization of adjuvants against the antigenic CH401 peptide in a simple preparatory manner. Overall, the co‐assembling vaccine design opens the door for efficient and practical self‐adjuvanting vaccine development. Abstract : A co‐assembled vaccine, composed of lipidated antigens and lipophilic adjuvants, is reported. This vaccine design possesses both antigen multivalency and antigen‐specific immunostimulation properties, and induces a robust immune response. This simple vaccine initiated a potent immune response without requiring complex synthesis, allowing efficient and practical development of self‐adjuvanting vaccines.
- Is Part Of:
- Angewandte Chemie international edition. Volume 59:Issue 40(2020)
- Journal:
- Angewandte Chemie international edition
- Issue:
- Volume 59:Issue 40(2020)
- Issue Display:
- Volume 59, Issue 40 (2020)
- Year:
- 2020
- Volume:
- 59
- Issue:
- 40
- Issue Sort Value:
- 2020-0059-0040-0000
- Page Start:
- 17705
- Page End:
- 17711
- Publication Date:
- 2020-08-11
- Subjects:
- adjuvants -- antigens -- cancer -- peptides -- self-assembly
Chemistry -- Periodicals
540 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3773 ↗
http://www.interscience.wiley.com/jpages/1433-7851 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/anie.202007999 ↗
- Languages:
- English
- ISSNs:
- 1433-7851
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0902.000500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 24188.xml