DNA fusion gene vaccines against cancer: from the laboratory to the clinic
DNA fusion gene vaccines against cancer: from the laboratory to the clinic
Vaccination against target antigens expressed by cancer cells has now become a realistic goal. DNA vaccines provide a direct link between identification of genetic markers in tumors and vaccine formulation. Simplicity of manufacture facilitates construction of vaccines against disease subsets or even for individual patients. To engage an immune system that exists to fight pathogens, we have developed fusion gene vaccines encoding tumor antigens fused to pathogen-derived sequences. This strategy activates high levels of T-cell help, the key to induction and maintenance of effective immunity. We have dissected the immunogenic tetanus toxin to obtain specific sequences able to activate antibody, CD4+, or CD8+ T cells to attack selected fused tumor antigens. Principles established in preclinical models are now being tested in patients. So far, objective immune responses against idiotypic antigen of neoplastic B cells have been observed in patients with B-cell malignancies and in normal transplant donors. These responses provide a platform for testing physical methods to improve DNA delivery and strategies to boost responses. For cancer, demands are high, because vaccines have to activate powerful immunity against weak antigens, often in a setting of immune damage or tolerance. Vaccination strategies against cancer and against microbes are sharing knowledge and technology for mutual benefit.
156-180
Stevenson, F.K.
ba803747-c0ac-409f-a9c2-b61fde009f8c
Rice, J.
d58d4fcd-8dc0-4599-bf96-62323d579227
Ottensmeier, C.H.
42b8a398-baac-4843-a3d6-056225675797
Thirdborough, S.M.
161784fb-c8e3-4beb-86b1-cd8bc8ddf8de
Zhu, D.
4f4f12ef-d220-4a7b-a1a0-63c6b66b9e17
2004
Stevenson, F.K.
ba803747-c0ac-409f-a9c2-b61fde009f8c
Rice, J.
d58d4fcd-8dc0-4599-bf96-62323d579227
Ottensmeier, C.H.
42b8a398-baac-4843-a3d6-056225675797
Thirdborough, S.M.
161784fb-c8e3-4beb-86b1-cd8bc8ddf8de
Zhu, D.
4f4f12ef-d220-4a7b-a1a0-63c6b66b9e17
Stevenson, F.K., Rice, J., Ottensmeier, C.H., Thirdborough, S.M. and Zhu, D.
(2004)
DNA fusion gene vaccines against cancer: from the laboratory to the clinic.
Immunological Reviews, 199, .
(doi:10.1111/j.0105-2896.2004.00145.x).
Abstract
Vaccination against target antigens expressed by cancer cells has now become a realistic goal. DNA vaccines provide a direct link between identification of genetic markers in tumors and vaccine formulation. Simplicity of manufacture facilitates construction of vaccines against disease subsets or even for individual patients. To engage an immune system that exists to fight pathogens, we have developed fusion gene vaccines encoding tumor antigens fused to pathogen-derived sequences. This strategy activates high levels of T-cell help, the key to induction and maintenance of effective immunity. We have dissected the immunogenic tetanus toxin to obtain specific sequences able to activate antibody, CD4+, or CD8+ T cells to attack selected fused tumor antigens. Principles established in preclinical models are now being tested in patients. So far, objective immune responses against idiotypic antigen of neoplastic B cells have been observed in patients with B-cell malignancies and in normal transplant donors. These responses provide a platform for testing physical methods to improve DNA delivery and strategies to boost responses. For cancer, demands are high, because vaccines have to activate powerful immunity against weak antigens, often in a setting of immune damage or tolerance. Vaccination strategies against cancer and against microbes are sharing knowledge and technology for mutual benefit.
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Published date: 2004
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Local EPrints ID: 26617
URI: http://eprints.soton.ac.uk/id/eprint/26617
ISSN: 0105-2896
PURE UUID: 56096f32-e2f1-4edb-a8e9-2e9ec7568a7e
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Date deposited: 20 Apr 2006
Last modified: 16 Mar 2024 02:54
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Author:
J. Rice
Author:
D. Zhu
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