Our overall strategy is to develop multivalent recombinant vaccines capable
of eliciting broad immune responses in patients with malignant melanoma or
colorectal cancer. We report herein results from initial studies conducted
in cancer patients to evaluate the effect of intratumoral administration o
f recombinant canarypox viruses carrying cytokine genes. Our current focus
is on the induction of tumor-specific T-cell responses using a prime/boost
immunization schedule with a unique vector system derived from the canary p
ox virus called ALVAC, in which we incorporate genes encoding Tumor Associa
ted Antigens (TAAs) of interest. Clinical studies in colorectal cancer eval
uating an ALVAC CEA candidate vaccine have shown that this approach is safe
and can induce tumor-specific T cell responses. Additional clinical studie
s evaluating candidate vaccines against melanoma and colorectal cancer, tar
geting either the gp100. Mage 1, Mage 3 or p53 molecules are ongoing, a 200
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