摘要
We have previously shown that tumor cellsgenetically modified to co-express IL-4 or IL-7 and B7.1have increased immunogenicity and provided vaccinessuperior to single gene transfectants or tumor cells/adjuvant mixture.Tumor antigens can be presented eitherdirectly by tumor cells or be indirectly represented byhost APC(cross-priming).Here we asked whether B7.1and IL-7 or IL-4 improved in an additive fashion one pathway of antigen presentation or complemented each other by improving preferentially different pathways of antigen presentation.
出处
《中国实验血液学杂志》
CAS
CSCD
1997年第3期310-310,共1页
Journal of Experimental Hematology