A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä
Recombination Monophosphoryl Lipid A-Derived Vacosome for the Development of Preventive Cancer Vaccines
Tekijät: Cheng RY, Fontana F, Xiao JY, Liu ZH, Figueiredo P, Shahbazi MA, Wang SQ, Jin J, Torrieri G, Hirvonen JT, Zhang HB, Chen TT, Cui WG, Lu Y, Santos HA
Kustantaja: American Chemical Society
Julkaisuvuosi: 2020
Journal: ACS Applied Materials and Interfaces
Tietokannassa oleva lehden nimi: ACS APPLIED MATERIALS & INTERFACES
Lehden akronyymi: ACS APPL MATER INTER
Vuosikerta: 12
Numero: 40
Aloitussivu: 44554
Lopetussivu: 44562
Sivujen määrä: 9
ISSN: 1944-8244
DOI: https://doi.org/10.1021/acsami.0c15057
Rinnakkaistallenteen osoite: https://research.utu.fi/converis/portal/detail/Publication/52138830
Recently, there has been an increasing interest for utilizing the host immune system to fight against cancer. Moreover, cancer vaccines, which can stimulate the host immune system to respond to cancer in the long term, are being investigated as a promising approach to induce tumor-specific immunity. In this work, we prepared an effective cancer vaccine (denoted as vacosome) by reconstructing the cancer cell membrane, monophosphoryl lipid A as a toll-like receptor 4 agonist, and egg phosphatidylcholine. The vacosome triggered and enhanced bone marrow dendritic cell maturation as well as stimulated the antitumor response against breast cancer 4T1 cells in vitro. Furthermore, an immune memory was established in BALB/c mice after three-time preimmunization with the vacosome. After that, the immunized mice showed inhibited tumor growth and prolonged survival period (longer than 50 days). Overall, our results demonstrate that the vacosome can be a potential candidate for clinical translation as a cancer vaccine.
Ladattava julkaisu This is an electronic reprint of the original article. |  |
