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Salmonella immunotherapy engineered with highly efficient tumor antigen coating establishes antigen-specific CD8+ T cell immunity and increases in antitumor efficacy with type I interferon combination therapy.
Wang, Suyang; Cheng, Michelle; Chen, Chao-Cheng; Chang, Chia-Yu; Tsai, Ya-Chea; Yang, Jr-Ming; Wu, T C; Huang, Chuan-Hsiang; Hung, Chien-Fu.
Affiliation
  • Wang S; Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
  • Cheng M; Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
  • Chen CC; Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
  • Chang CY; Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
  • Tsai YC; Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
  • Yang JM; Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
  • Wu TC; Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
  • Huang CH; Department of Oncology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
  • Hung CF; Department of Obstetrics and Gynecology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Oncoimmunology ; 13(1): 2298444, 2024.
Article in En | MEDLINE | ID: mdl-38170154
ABSTRACT
Bacteria-based cancer therapy employs various strategies to combat tumors, one of which is delivering tumor-associated antigen (TAA) to generate specific immunity. Here, we utilized a poly-arginine extended HPV E7 antigen (9RE7) for attachment on Salmonella SL7207 outer membrane to synthesize the bacterial vaccine Salmonella-9RE7 (Sal-9RE7), which yielded a significant improvement in the amount of antigen presentation compared to the previous lysine-extended antigen coating strategy. In TC-1 tumor mouse models, Sal-9RE7 monotherapy decreased tumor growth by inducing E7 antigen-specific immunity. In addition, pairing Sal-9RE7 with adjuvant Albumin-IFNß (Alb-IFNß), a protein cytokine fusion, the combination significantly increased the antitumor efficacy and enhanced immunogenicity in the tumor microenvironment (TME). Our study made a significant contribution to personalized bacterial immunotherapy via TAA delivery and demonstrated the advantage of combination therapy.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Interferon Type I / Neoplasms Limits: Animals Language: En Journal: Oncoimmunology Year: 2024 Document type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Interferon Type I / Neoplasms Limits: Animals Language: En Journal: Oncoimmunology Year: 2024 Document type: Article Affiliation country: United States
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