TGFβ-derived immune modulatory vaccine: targeting the immunosuppressive and fibrotic tumor microenvironment in a murine model of pancreatic cancer.
Mice
Animals
CD8-Positive T-Lymphocytes
Cancer Vaccines
Transforming Growth Factor beta
Tumor Microenvironment
Disease Models, Animal
Cell Line, Tumor
Vaccines, Subunit
/ therapeutic use
Mice, Inbred C57BL
Pancreatic Neoplasms
/ metabolism
Carcinoma, Pancreatic Ductal
/ genetics
Immunosuppressive Agents
/ therapeutic use
Immunity
Fibrosis
Pancreatic Neoplasms
Immunogenicity, Vaccine
Immunotherapy
Tumor Microenvironment
Vaccination
Journal
Journal for immunotherapy of cancer
ISSN: 2051-1426
Titre abrégé: J Immunother Cancer
Pays: England
ID NLM: 101620585
Informations de publication
Date de publication:
12 2022
12 2022
Historique:
accepted:
06
11
2022
entrez:
5
1
2023
pubmed:
6
1
2023
medline:
7
1
2023
Statut:
ppublish
Résumé
Pancreatic ductal adenocarcinoma (PDAC) is associated with very poor survival, making it the third and fourth leading cause of all cancer-related deaths in the USA and European Union, respectively. The tumor microenvironment (TME) in PDAC is highly immunosuppressive and desmoplastic, which could explain the limited therapeutic effect of immunotherapy in PDAC. One of the key molecules that contributes to immunosuppression and fibrosis is transforming growth factor-β (TGFβ). The aim of this study was to target the immunosuppressive and fibrotic TME in PDAC using a novel immune modulatory vaccine with TGFβ-derived peptides in a murine model of pancreatic cancer. C57BL/6 mice were subcutaneously inoculated with Pan02 PDAC cells. Mice were treated with TGFβ1-derived peptides (major histocompatibility complex (MHC)-I and MHC-II-restricted) adjuvanted with Montanide ISA 51VG. The presence of treatment-induced TGFβ-specific T cells was assessed by ELISpot (enzyme-linked immunospot). Changes in the immune infiltration and gene expression profile in tumor samples were characterized by flow cytometry, reverse transcription-quantitative PCR (RT-qPCR), and bulk RNA sequencing. Treatment with immunogenic TGFβ-derived peptides was safe and controlled tumor growth in Pan02 tumor-bearing mice. Enlargement of tumor-draining lymph nodes in vaccinated mice positively correlated to the control of tumor growth. Analysis of immune infiltration and gene expression in Pan02 tumors revealed that TGFβ-derived peptide vaccine increased the infiltration of CD8 This study demonstrates the antitumor activity of TGFβ-derived multipeptide vaccination in a murine tumor model of PDAC. The data suggest that the vaccine targets immunosuppression and fibrosis in the TME by polarizing the cellular composition towards a more pro-inflammatory phenotype. Our findings support the feasibility and potential of TGFβ-derived peptide vaccination as a novel immunotherapeutic approach to target immunosuppression in the TME.
Sections du résumé
BACKGROUND
Pancreatic ductal adenocarcinoma (PDAC) is associated with very poor survival, making it the third and fourth leading cause of all cancer-related deaths in the USA and European Union, respectively. The tumor microenvironment (TME) in PDAC is highly immunosuppressive and desmoplastic, which could explain the limited therapeutic effect of immunotherapy in PDAC. One of the key molecules that contributes to immunosuppression and fibrosis is transforming growth factor-β (TGFβ). The aim of this study was to target the immunosuppressive and fibrotic TME in PDAC using a novel immune modulatory vaccine with TGFβ-derived peptides in a murine model of pancreatic cancer.
METHODS
C57BL/6 mice were subcutaneously inoculated with Pan02 PDAC cells. Mice were treated with TGFβ1-derived peptides (major histocompatibility complex (MHC)-I and MHC-II-restricted) adjuvanted with Montanide ISA 51VG. The presence of treatment-induced TGFβ-specific T cells was assessed by ELISpot (enzyme-linked immunospot). Changes in the immune infiltration and gene expression profile in tumor samples were characterized by flow cytometry, reverse transcription-quantitative PCR (RT-qPCR), and bulk RNA sequencing.
RESULTS
Treatment with immunogenic TGFβ-derived peptides was safe and controlled tumor growth in Pan02 tumor-bearing mice. Enlargement of tumor-draining lymph nodes in vaccinated mice positively correlated to the control of tumor growth. Analysis of immune infiltration and gene expression in Pan02 tumors revealed that TGFβ-derived peptide vaccine increased the infiltration of CD8
CONCLUSION
This study demonstrates the antitumor activity of TGFβ-derived multipeptide vaccination in a murine tumor model of PDAC. The data suggest that the vaccine targets immunosuppression and fibrosis in the TME by polarizing the cellular composition towards a more pro-inflammatory phenotype. Our findings support the feasibility and potential of TGFβ-derived peptide vaccination as a novel immunotherapeutic approach to target immunosuppression in the TME.
Identifiants
pubmed: 36600556
pii: jitc-2022-005491
doi: 10.1136/jitc-2022-005491
pmc: PMC9730419
pii:
doi:
Substances chimiques
Cancer Vaccines
0
Transforming Growth Factor beta
0
Vaccines, Subunit
0
Immunosuppressive Agents
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Informations de copyright
© Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.
Déclaration de conflit d'intérêts
Competing interests: MHA has made an invention based on the use of transforming growth factor-β-derived peptides for vaccinations. A patent application directed to the invention is owned by the company IO Biotech ApS and lists MHA as the sole inventor. MHA is advisor and shareholder at IO Biotech. IL and EM are employees at IO Biotech. The additional authors declare no competing financial interests.
Références
Oncoimmunology. 2020 Jun 1;9(1):1771142
pubmed: 32923127
Nat Commun. 2017 Apr 27;8:15095
pubmed: 28447602
Oncoimmunology. 2018 Aug 1;7(9):e1462431
pubmed: 30228932
Oncoimmunology. 2015 Sep 11;5(4):e1085147
pubmed: 27141376
Cancer Immunol Res. 2021 Nov;9(11):1316-1326
pubmed: 34518197
Nat Rev Clin Oncol. 2020 Sep;17(9):527-540
pubmed: 32398706
Cell Commun Signal. 2021 Nov 24;19(1):117
pubmed: 34819086
Cancer Immunol Immunother. 2019 Nov;68(11):1901-1907
pubmed: 31690955
Cancers (Basel). 2021 Jan 25;13(3):
pubmed: 33503832
Nat Med. 2021 Dec;27(12):2212-2223
pubmed: 34887574
Cancers (Basel). 2021 Aug 17;13(16):
pubmed: 34439292
Oncotarget. 2016 Jan 5;7(1):323-41
pubmed: 26586478
Chronic Dis Transl Med. 2020 Feb 11;6(1):6-17
pubmed: 32226930
Cancer Immunol Res. 2016 Jan;4(1):18-25
pubmed: 26563311
Blood. 2011 Feb 17;117(7):2200-10
pubmed: 21079151
Mol Cell Proteomics. 2021;20:100022
pubmed: 33583769
J Oncol. 2022 Mar 15;2022:9749363
pubmed: 35342400
Matrix Biol. 2018 Aug;68-69:28-43
pubmed: 29288716
Oncotarget. 2015 Apr 10;6(10):7504-21
pubmed: 25762644
Nat Methods. 2015 May;12(5):453-7
pubmed: 25822800
Cancer Discov. 2019 Aug;9(8):1102-1123
pubmed: 31197017
Mol Cancer. 2018 Jan 11;17(1):5
pubmed: 29325547
Oncoimmunology. 2022 Jan 27;11(1):2026020
pubmed: 35111385
Cell Mol Immunol. 2021 Nov;18(11):2575-2577
pubmed: 34526675
Ann Oncol. 2022 Mar;33(3):330-339
pubmed: 35090748
World J Gastrointest Oncol. 2021 Jun 15;13(6):472-494
pubmed: 34163568
J Immunother Cancer. 2020 Jul;8(2):
pubmed: 32690770
Bioinformatics. 2016 Feb 15;32(4):511-7
pubmed: 26515819
Semin Immunopathol. 2019 Jan;41(1):87-95
pubmed: 29968045
J Exp Clin Cancer Res. 2019 Mar 6;38(1):115
pubmed: 30841909
Sci Rep. 2017 Jan 13;7:40508
pubmed: 28084418
Sci Rep. 2022 Jul 11;12(1):11748
pubmed: 35817787
Trends Cancer. 2019 Nov;5(11):724-741
pubmed: 31735290
Sci Rep. 2020 Oct 2;10(1):16425
pubmed: 33009477
Cancer Res. 2018 Mar 15;78(6):1379-1382
pubmed: 29440147
Nat Commun. 2020 Dec 9;11(1):6315
pubmed: 33298926
Immunity. 2019 Apr 16;50(4):924-940
pubmed: 30995507
J Clin Oncol. 2022 Sep 20;40(27):3180-3189
pubmed: 35476508
Nat Rev Cancer. 2016 Aug 23;16(9):582-98
pubmed: 27550820
World J Gastroenterol. 2021 Jul 21;27(27):4298-4321
pubmed: 34366606
Front Oncol. 2021 Oct 29;11:771488
pubmed: 34778091
Oncogene. 2022 Feb;41(9):1364-1375
pubmed: 35017664
Front Immunol. 2021 Dec 08;12:791453
pubmed: 34956223
Oncoimmunology. 2013 Apr 1;2(4):e23991
pubmed: 23734334
Cold Spring Harb Perspect Biol. 2016 Jun 01;8(6):
pubmed: 27252363
J Immunother. 2009 Jan;32(1):12-21
pubmed: 19307989
Nat Commun. 2018 Nov 8;9(1):4692
pubmed: 30410077
Br J Cancer. 2018 Nov;119(10):1208-1214
pubmed: 30318515
Cancers (Basel). 2021 Oct 11;13(20):
pubmed: 34680235
Cell Mol Immunol. 2021 Feb;18(2):415-426
pubmed: 33408343
Semin Immunopathol. 2017 Apr;39(3):317-326
pubmed: 27677755