optotic necrotic by radiation. Upon phagocytosis, we analyzed DCs maturation through the e pression of sur face markers and the decrease of the endocytic capacity, in vitro migration in response to chemokines and, most importantly, demonstrated their ability to cross present native tumor Ags to specific CTLs in vitro. Methods Cell lines and clones Four human melanoma cell lines were used in this study. Mel Y1, Mel Y2, Mel Y3 and Mel 4 were cultured in melanoma medium supplemented with 2 mM glutamine, 20 nM sodium selenite, 100 M ascorbic acid, 0. 3 mg ml galactose, 0. 15 mg ml sodium pyruvate and 5 g ml insulin, 100 IU ml penicillin, 10 g ml strep tomycin plus 10% fetal bovine serum in a GMP core facility at the Centro de Investigaciones Oncol��gicas FUCA.

CTL clones specific for MelanA MART 1 and gp100 Ags were e panded in RPMI medium in 14 day cycles by using 30 ng ml anti CD3 antibody and serial 300 UI ml IL 2 every Anacetrapib 3 days plus 10% heat inactivated AB human serum and antibiotics. Cell lines were periodically tested to be mycoplasma free. Preparation of tumor apoptotic necrotic cells Apoptotic necrotic tumor cells were pre pared as a batch of four cell lines from master cell banks after safety testing for mycoplasma, viruses and bacteria. All cell lines e press Tyrosinase, MAGE 3, MelanA MART 1, TRP 2, gp100, GD2, GD3 and NY ESO 1 by RT PCR and or immunocytochemistry . After gamma irradiation at 70 Gy, the cells were frozen in liquid nitrogen until use. Cells were then thawed and plated in melanoma medium plus 10% FBS to complete the apoptotic process.

After 72 hs the cells were detached from the flasks, washed, counted and resuspended in fresh serum free AIM V Medium. Apoptosis and necrosis were assessed by Anne in V and Propidium iodide binding and Flow Cytometric anal ysis. A soft agar clonogenic assay performed in se tuplicate was used to test that irradiated cells have lost their proliferation ability compared to non irradiated control cells. Generation of DCs from monocytes DCs were generated from buffy coats or leukapheresis products obtained from healthy donors at the Hemother apy Department of the Instituto Ale ander Fleming. Peripheral blood mononuclear cells were puri fied by Fycoll Hypaque density centrifugation. PBMCs were resuspended in AIM V medium and allowed to adhere to 0. 22 m filter capped culture flasks.

After 2 hs at 37 C, the non adherent cells were removed, and adherent monocytes were subsequently cul tured for 5 days in AIM V supplemented with 800 U ml rhuGM CSF and 50 ng ml IL 4. Phenotypic changes were monitored by light microscopy and FACS. To induce control DCs matu ration, 2 g ml LPS was added and the cells were further cultured for 48 hs. DCs phenotype Characterization of DCs phenotype was performed at the immature state and after Apo Nec phagocytosis by staining 5 105 cells with fluorochrome labeled antibod ies against CD14, CD11c, CD1a, HLA DR DP DQ, CD80, CD86, CD83, CD40, HLA ABC and CCR7, and FACS anal ysis wa