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DNA fusion vaccines enter the clinic

DNA fusion vaccines enter the clinic
DNA fusion vaccines enter the clinic
Induction of effective immune attack on cancer cells in patients requires conversion of weak tumor antigens into strong immunogens. Our strategy employs genetic technology to create DNA vaccines containing tumor antigen sequences fused to microbial genes. The fused microbial protein engages local CD4+ T cells to provide help for anti-tumor immunity, and to reverse potential regulation. In this review, we focus on induction of CD8+ T cells able to kill target tumor cells. The DNA vaccines incorporate tumor-derived peptide sequences fused to an engineered domain of tetanus toxin. In multiple models, this design induces strong CD8+ T-cell responses, able to suppress tumor growth. For clinical relevance, we have used "humanized" mice expressing HLA-A2, successfully inducing cytolytic T-cell responses against a range of candidate human peptides. To overcome physical restriction in translating to patients, we have used electroporation. Clinical trials of patients with cancer are showing induction of responses, with preliminary indications of suppression of tumor growth and evidence for clinically manageable concomitant autoimmunity.
0340-7004
1147-1151
Stevenson, Freda K.
ba803747-c0ac-409f-a9c2-b61fde009f8c
Mander, Ann
2fcb3a33-6bb8-4463-8b06-79cd508e9d80
Chudley, Lindsey
ec25c30c-369d-4516-b872-4cb3c135c10a
Ottensmeier, Christian H.
42b8a398-baac-4843-a3d6-056225675797
Stevenson, Freda K.
ba803747-c0ac-409f-a9c2-b61fde009f8c
Mander, Ann
2fcb3a33-6bb8-4463-8b06-79cd508e9d80
Chudley, Lindsey
ec25c30c-369d-4516-b872-4cb3c135c10a
Ottensmeier, Christian H.
42b8a398-baac-4843-a3d6-056225675797

Stevenson, Freda K., Mander, Ann, Chudley, Lindsey and Ottensmeier, Christian H. (2011) DNA fusion vaccines enter the clinic. Cancer Immunology Immunotherapy, 60 (8), 1147-1151. (doi:10.1007/s00262-011-1042-2). (PMID:21644035)

Record type: Article

Abstract

Induction of effective immune attack on cancer cells in patients requires conversion of weak tumor antigens into strong immunogens. Our strategy employs genetic technology to create DNA vaccines containing tumor antigen sequences fused to microbial genes. The fused microbial protein engages local CD4+ T cells to provide help for anti-tumor immunity, and to reverse potential regulation. In this review, we focus on induction of CD8+ T cells able to kill target tumor cells. The DNA vaccines incorporate tumor-derived peptide sequences fused to an engineered domain of tetanus toxin. In multiple models, this design induces strong CD8+ T-cell responses, able to suppress tumor growth. For clinical relevance, we have used "humanized" mice expressing HLA-A2, successfully inducing cytolytic T-cell responses against a range of candidate human peptides. To overcome physical restriction in translating to patients, we have used electroporation. Clinical trials of patients with cancer are showing induction of responses, with preliminary indications of suppression of tumor growth and evidence for clinically manageable concomitant autoimmunity.

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More information

Published date: August 2011
Organisations: Cancer Sciences

Identifiers

Local EPrints ID: 337159
URI: http://eprints.soton.ac.uk/id/eprint/337159
ISSN: 0340-7004
PURE UUID: 0c364a04-8185-466d-a358-aceb20761182
ORCID for Freda K. Stevenson: ORCID iD orcid.org/0000-0002-0933-5021

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Date deposited: 19 Apr 2012 14:11
Last modified: 15 Mar 2024 02:53

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Contributors

Author: Ann Mander
Author: Lindsey Chudley

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