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Commentary |
Department of Oncology, Gastroenterology, Endocrinology and Metabolism, Division of Oncology, St George's Hospital Medical School, Cranmer Terrace, London SW17 0RE, UK
Over the past decade there has been a widespread resurgence of interest in the concept of cancer immunotherapy and the design of new cancer vaccines. The discovery of tumour specific and tumour associated antigens has resulted in a large number of targets that are currently being developed as potential clinical products. These are comprehensively reviewed by Jäger et al.1
Although the identification of tumour antigen epitopes by cytotoxic T lymphocytes (CTL) is certainly an elegant and logical approach, there is a disturbing lack of correlation between CTL activity to these epitopes and clinical response.2 Moreover, it seems that there is a distinctive lack of help for a second signal in many reductionistic approaches because responses are often seen only after the addition of interleukin 2 (IL-2).3
In addition to specific immune responses, it may be that an appropriate innate immune response is as important or more important for cancer
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