A universal anti-cancer vaccine

• Verfasst von: Sharbi Yunger, Adi [VerfasserIn]
• Verfasst von: Grees, Mareike [VerfasserIn]
• Verfasst von: Eichmüller, Stefan B. [VerfasserIn]
• Verfasst von: Utikal, Jochen [VerfasserIn]
• Verfasst von: Umansky, Viktor [VerfasserIn]
• Verfasst von: Eisenbach, Lea [VerfasserIn]
• Titel: A universal anti-cancer vaccine
• Titelzusatz: Chimeric invariant chain potentiates the inhibition of melanoma progression and the improvement of survival
• Verf.angabe: Adi Sharbi‐Yunger, Mareike Grees, Gal Cafri, David Bassan, Stefan B. Eichmüller, Esther Tzehoval, Jochen Utikal, Viktor Umansky and Lea Eisenbach
• Jahr: 2019
• Umfang: 13 S.
• Fussnoten: Online 14 Aug 2018 ; Gesehen am 19.02.2019
• Titel Quelle: Enthalten in: International journal of cancer
• Ort Quelle: Bognor Regis : Wiley-Liss, 1966
• Jahr Quelle: 2019
• Band/Heft Quelle: 144(2019), 4, Seite 909-921
• ISSN Quelle: 1097-0215
• DOI: doi:10.1002/ijc.31795
• Datenträger: Online-Ressource
• Sprache: eng
• Sach-SW: chimeric construct
• Sach-SW: dendritic Cells
• Sach-SW: melanoma
• Sach-SW: MHC Class II
• Sach-SW: mRNA
• Sach-SW: vaccine
• K10plus-PPN: 158780638X

Abstract

For many years, clinicians and scientists attempt to develop methods to stimulate the immune system to target malignant cells. Recent data suggest that effective cancer vaccination requires combination immunotherapies to overcome tumor immune evasion. Through presentation of both MHC-I and II molecules, DCs-based vaccine platforms are effective in generating detectable CD4 and CD8 T cell responses against tumor-associated antigens. Several platforms include DC transfection with mRNA of the desired tumor antigen. These DCs are then delivered to the host and elicit an immune response against the antigen of interest. We have recently established an mRNA genetic platform which induced specific CD8+ cytotoxic T cell response by DC vaccination against melanoma. In our study, an MHC-II mRNA DCs vaccine platform was developed to activate CD4+ T cells and to enhance the anti-tumor response. The invariant chain (Ii) was modified and the semi-peptide CLIP was replaced with an MHC-II binding peptide sequences of melanoma antigens. These chimeric MHC-II constructs are presented by DCs and induce proliferation of tumor specific CD4+ T cells. When administered in combination with the MHC-I platform into tumor bearing mice, these constructs were able to inhibit tumor growth, and improve mouse survival. Deciphering the immunological mechanism of action, we observed an efficient CTLs killing in addition to higher levels of Th1 and Th2 subsets in the groups immunized with a combination of the MHC-I and MHC-II constructs. These universal constructs can be applied in multiple combinations and offer an attractive opportunity to improve cancer treatment.