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Journal of Experimental Hematology ; (6): 1178-1182, 2006.
文章 在 中文 | WPRIM | ID: wpr-282705

摘要

The purpose of this study was to construct a HA-1-DC nucleic acid vaccine and to induce anti-leukemia effect after hematopoietic stem cell transplantation (HSCT). The dendritic cells (DCs) were generated from HSCT donors in vitro, and its immunologic activity was studied by using flow cytometry and mix lymphocyte reaction. HA-1 gene was electroporated into the cultured DCs to construct a DC nucleic acid vaccine. After transfecting for 48 hours, the expression of HA-1 protein was detected by Western blot. The DCs were cultured with isogenic lymphocytes to induce specific cytotoxic T lymphocytes (CTLs). The cytotoxicity of the CTLs was detected by LDH assay. The results showed that the DCs derived from peripheral blood monocytes (PBMCs) expressed the DC phenotype, and were effective in stimulating proliferation of the allogenic lymphocytes. After electroporating for 48 hours, HA-1 protein was detected by Western blot. The cytotoxity of inducing CTLs was higher than that in the control group. It is concluded that the minor histocompatibility antigen HA-1 can be considered as a target of immunotherapy against leukemia after HSCT.


Subject(s)
Humans , Cancer Vaccines , Genetics , Allergy and Immunology , Cells, Cultured , Dendritic Cells , Cell Biology , Allergy and Immunology , Electroporation , Graft vs Host Disease , Hematopoietic Stem Cell Transplantation , Leukemia , Allergy and Immunology , Therapeutics , Minor Histocompatibility Antigens , Genetics , Allergy and Immunology , Oligopeptides , Genetics , Allergy and Immunology , T-Lymphocytes, Cytotoxic , Allergy and Immunology , Transfection , Vaccines, DNA , Genetics , Allergy and Immunology
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