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Editorial
. 2005 Apr 29;3(1):18.
doi: 10.1186/1479-5876-3-18.

Progress and controversies in developing cancer vaccines

Affiliations
Editorial

Progress and controversies in developing cancer vaccines

Craig L Slingluff Jr et al. J Transl Med. .

Abstract

Immunotherapy has become a standard approach for cancer management, through the use of cytokines (eg: interleukin-2) and monoclonal antibodies. Cancer vaccines hold promise as another form of immunotherapy, and there has been substantial progress in identifying shared antigens recognized by T cells, in developing vaccine approaches that induce antigen-specific T cell responses in cancer patients, and in developing new technology for monitoring immune responses in various human tissue compartments. Dramatic clinical regressions of human solid tumors have occurred with some cancer vaccines, but the rate of those responses remains low. This article is part of a 2-part point:counterpoint series on peptide vaccines and adoptive therapy approaches for cancer. The current status of cancer vaccination, and associated challenges, are discussed. Emphasis is placed on the need to increase our knowledge of cancer immunobiology, as well as to improve monitoring of cellular immune function after vaccination. Progress in both areas will facilitate development of effective cancer vaccines, as well as of adoptive therapy. Effective cancer vaccines promise to be useful for treatment and prevention of cancer at low cost and with low morbidity.

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References

    1. Coley WB. Further observations upon the treatment of malignant tumors with the toxins of erysipelas and Bacillus prodigiosus with a report of 160 cases. Bull Johns Hopkins Hosp. 1896;7:157.
    1. Fehleisen F. Uber die Zuchtung der Erysipel-Kokken auf Kunstlichen Nahrboden und die Ubertragbarkeit auf den Menschen. Deutsche Med Wschr. 1882;8:533.
    1. Agarwala SS, Neuberg D, Park Y, Kirkwood JM. Mature Results of a Phase III Randomized Trial of Bacillus Calmette-Guerin (BCG) versus Observation and BCG plus Dacarbazine versus BCG in the Adjuvant Therapy of American Joint Committee on Cancer Stage I-III Melanoma (E1673) A Trial of the Eastern Cooperative Oncology Group. Cancer. 2004;100:1692–8. doi: 10.1002/cncr.20166. - DOI - PubMed
    1. Morton DL. Adjuvant immunotherapy of malignant melanoma; Status of clinical trials at UCLA. Int J Immunother. 1986;2:31.
    1. Seigler HF, Cox E, Mutzner F, Shepherd L, Nicholson E, Shingleton WW. Specific active immunotherapy for melanoma. Ann Surg. 1979;190:366–372. - PMC - PubMed

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