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In vivo antigen delivery by a Salmonella typhimurium type III secretion system for therapeutic cancer vaccines
Hiroyoshi Nishikawa, … , Jorge E. Galán, Sacha Gnjatic
Hiroyoshi Nishikawa, … , Jorge E. Galán, Sacha Gnjatic
Published July 3, 2006
Citation Information: J Clin Invest. 2006;116(7):1946-1954. https://doi.org/10.1172/JCI28045.
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Research Article

In vivo antigen delivery by a Salmonella typhimurium type III secretion system for therapeutic cancer vaccines

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Abstract

Bacterial vectors may offer many advantages over other antigen delivery systems for cancer vaccines. We engineered a Salmonella typhimuriumvaccine strain to deliver the NY-ESO-1 tumor antigen (S. typhimurium–NY-ESO-1) through a type III protein secretion system. The S. typhimurium–NY-ESO-1 construct elicited NY-ESO-1–specific CD8+ and CD4+ T cells from peripheral blood lymphocytes ofcancer patients in vitro. Oral administration of S. typhimurium–NY-ESO-1 to mice resulted in the regression of established NY-ESO-1–expressing tumors. Intratumoral inoculation of S. typhimurium–NY-ESO-1 to NY-ESO-1–negative tumors resulted in delivery of antigen in vivo and led to tumor regression in the presence of preexisting NY-ESO-1–specific CD8+ T cells. Specific T cell responses against at least 2 unrelated tumor antigens not contained in the vaccine were observed, demonstrating epitope spreading. We propose that antigen delivery through the S. typhimuriumtype III secretion system is a promising novel strategy for cancer vaccine development.

Authors

Hiroyoshi Nishikawa, Eiichi Sato, Gabriel Briones, Li-Mei Chen, Mitsutoshi Matsuo, Yasuhiro Nagata, Gerd Ritter, Elke Jäger, Hideki Nomura, Shigeto Kondo, Isao Tawara, Takuma Kato, Hiroshi Shiku, Lloyd J. Old, Jorge E. Galán, Sacha Gnjatic

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Figure 3

S. typhimurium type III secretion system induces antigen-specific primary CD8+ T cells from PBMCs.

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S. typhimurium
                  type III secretion system induces anti...
(A) CD8+ T cells derived from PBMCs of NW29 and NW634 were presensitized by CD4–CD8– PBMCs infected with S. typhimurium–NY-ESO-1 or the control strain as described in Methods, and induction of specific CD8+ T cells was analyzed by ELISPOT assay for recognition of autologous EBV-B cells pulsed with peptides or infected with recombinant Fowlpox (rFowlpox) virus. Data are mean ± SD. (B) NY-ESO-1–specific CD8+ T cells induced from NW29 were stained with NY-ESO-192–100/HLA-Cw*0304 tetramer–PE and anti-CD8–Tricolor and analyzed by flow cytometry. Experiments were performed independently at least twice with similar results. Percentages indicate frequency of tetramer-stained cells within CD8+ cells.

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ISSN: 0021-9738 (print), 1558-8238 (online)

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