Upon tumour antigen pulsing, high levels of chemokines that sustain the recruitment of circulating DCs to inflamed tissues, such as CCL3, CCL4, were expressed, whereas at late time-points constitutive lymphoid chemokine such as CCL2, CCL8, CXCL10, CXCL12 and RANTES were selectively up-regulated. This evidence concerns the gene CXCL10 and neoplasm.