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MF59 formulated with CpG ODN as a potent adjuvant of recombinant HSP65-MUC1 for inducing anti-MUC1(+) tumor immunity in mice

MF59 is an oil-in-water emulsion adjuvant approved for influenza vaccines for human use in Europe. Due to its Th2 inducing properties, MF59 is seldom tested for cancer vaccines. In this study, MF59 formulated with a C-type CpG oligodeoxynucleotide (YW002) was tested for its Th1 adjuvant activity to...

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Autores principales: Yang, Ming, Yan, Youyou, Fang, Mingli, Wan, Min, Wu, Xiuli, Zhang, Xiaoling, Zhao, Tiesuo, Wei, Hongfei, Song, Dandan, Wang, Liying, Yu, Yongli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7106219/
https://www.ncbi.nlm.nih.gov/pubmed/22595192
http://dx.doi.org/10.1016/j.intimp.2012.05.003
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author Yang, Ming
Yan, Youyou
Fang, Mingli
Wan, Min
Wu, Xiuli
Zhang, Xiaoling
Zhao, Tiesuo
Wei, Hongfei
Song, Dandan
Wang, Liying
Yu, Yongli
author_facet Yang, Ming
Yan, Youyou
Fang, Mingli
Wan, Min
Wu, Xiuli
Zhang, Xiaoling
Zhao, Tiesuo
Wei, Hongfei
Song, Dandan
Wang, Liying
Yu, Yongli
author_sort Yang, Ming
collection PubMed
description MF59 is an oil-in-water emulsion adjuvant approved for influenza vaccines for human use in Europe. Due to its Th2 inducing properties, MF59 is seldom tested for cancer vaccines. In this study, MF59 formulated with a C-type CpG oligodeoxynucleotide (YW002) was tested for its Th1 adjuvant activity to induce immune responses to HSP65-MUC1, a recombinant fusion protein incorporating a mycobacterial heat shock protein (HSP65) and mucin 1, cell surface associated (MUC1) derived peptide. Combination of YW002 with MF59 (MF59-YW002) could confer a potent Th1 biasing property to the adjuvant, which enhanced the immunogenicity of HSP65-MUC1 to induce significantly higher levels of specific IgG2c, increased IFN-γ mRNA expression in splenocytes and the generation of antigen-specific cytotoxic T lymphocytes in mice. When prophylactically applied, MF59-YW002 adjuvant containing HSP65-MUC1 inhibited the growth of MUC1(+) B16 melanoma and prolonged the survival of tumor-bearing mice. In contrast, adjuvant containing MF59 with HSP65-MUC1 in the absence of YW002, promoted the growth of MUC1(+) B16 melanoma in mice. These results suggest that MF59 plus CpG oligodeoxynucleotide might be developed as an efficient adjuvant for tumor vaccines against melanoma, and possibly other tumors.
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spelling pubmed-71062192020-03-31 MF59 formulated with CpG ODN as a potent adjuvant of recombinant HSP65-MUC1 for inducing anti-MUC1(+) tumor immunity in mice Yang, Ming Yan, Youyou Fang, Mingli Wan, Min Wu, Xiuli Zhang, Xiaoling Zhao, Tiesuo Wei, Hongfei Song, Dandan Wang, Liying Yu, Yongli Int Immunopharmacol Article MF59 is an oil-in-water emulsion adjuvant approved for influenza vaccines for human use in Europe. Due to its Th2 inducing properties, MF59 is seldom tested for cancer vaccines. In this study, MF59 formulated with a C-type CpG oligodeoxynucleotide (YW002) was tested for its Th1 adjuvant activity to induce immune responses to HSP65-MUC1, a recombinant fusion protein incorporating a mycobacterial heat shock protein (HSP65) and mucin 1, cell surface associated (MUC1) derived peptide. Combination of YW002 with MF59 (MF59-YW002) could confer a potent Th1 biasing property to the adjuvant, which enhanced the immunogenicity of HSP65-MUC1 to induce significantly higher levels of specific IgG2c, increased IFN-γ mRNA expression in splenocytes and the generation of antigen-specific cytotoxic T lymphocytes in mice. When prophylactically applied, MF59-YW002 adjuvant containing HSP65-MUC1 inhibited the growth of MUC1(+) B16 melanoma and prolonged the survival of tumor-bearing mice. In contrast, adjuvant containing MF59 with HSP65-MUC1 in the absence of YW002, promoted the growth of MUC1(+) B16 melanoma in mice. These results suggest that MF59 plus CpG oligodeoxynucleotide might be developed as an efficient adjuvant for tumor vaccines against melanoma, and possibly other tumors. Elsevier B.V. 2012-08 2012-05-14 /pmc/articles/PMC7106219/ /pubmed/22595192 http://dx.doi.org/10.1016/j.intimp.2012.05.003 Text en Copyright © 2012 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Yang, Ming
Yan, Youyou
Fang, Mingli
Wan, Min
Wu, Xiuli
Zhang, Xiaoling
Zhao, Tiesuo
Wei, Hongfei
Song, Dandan
Wang, Liying
Yu, Yongli
MF59 formulated with CpG ODN as a potent adjuvant of recombinant HSP65-MUC1 for inducing anti-MUC1(+) tumor immunity in mice
title MF59 formulated with CpG ODN as a potent adjuvant of recombinant HSP65-MUC1 for inducing anti-MUC1(+) tumor immunity in mice
title_full MF59 formulated with CpG ODN as a potent adjuvant of recombinant HSP65-MUC1 for inducing anti-MUC1(+) tumor immunity in mice
title_fullStr MF59 formulated with CpG ODN as a potent adjuvant of recombinant HSP65-MUC1 for inducing anti-MUC1(+) tumor immunity in mice
title_full_unstemmed MF59 formulated with CpG ODN as a potent adjuvant of recombinant HSP65-MUC1 for inducing anti-MUC1(+) tumor immunity in mice
title_short MF59 formulated with CpG ODN as a potent adjuvant of recombinant HSP65-MUC1 for inducing anti-MUC1(+) tumor immunity in mice
title_sort mf59 formulated with cpg odn as a potent adjuvant of recombinant hsp65-muc1 for inducing anti-muc1(+) tumor immunity in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7106219/
https://www.ncbi.nlm.nih.gov/pubmed/22595192
http://dx.doi.org/10.1016/j.intimp.2012.05.003
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