A. Carr (Center of Molecular Immunology, Havana, Cuba). L1210 murine lymphocytic leukemia cell line was obtained

from the American Tissue Type Culture Collection. L1210 cmah-kd cell line was generated in our institution as previously described [46] by CMP-Neu5Ac-neuraminic acid hydroxylase gene knock-down using a specific shRNA. Cells were grown in DMEM (Gibco-BRL, Paisley, UK) supplemented with 10% heat-inactivated FCS (Invitrogen, USA), 2 mM L-glutamine, 25 mM HEPES, 100 U/mL penicillin, 100 μg/mL streptomycin, and maintained at 37°C with 5% CO2. L1210 cells were treated with trypsin (Gibco) 0.05% for 5 min at 37°C for testing the importance of the gangliosides in binding and cytotoxicity experiments. Fresh blood from healthy volunteers was centrifuged over a Ficoll-Hypaque see more density gradient to obtain PBMCs as described earlier [47]. One hundred normal serum samples were obtained from healthy adults of both genders and various ethnic backgrounds. None of the donors presented the evidence of infectious disease, cancer, atherosclerosis, or autoimmune diseases at the

time of blood collection. Cancer patients’ Cisplatin manufacturer sera were obtained from 53 advanced NSCLC patients who had not been exposed to any antitumor treatment, with approval from the Institutional Review Board of the Hermanos Ameijeiras Hospital. The cancer patients were gender- and age-matched with the healthy donors. Written informed consent was obtained in advance from all the volunteers. The serum samples were decomplemented by heat inactivation for 30 min at 56°C. All sera were stored at –20°C until use. Anti-NeuGcGM3

antibodies present in human sera were detected by ELISA with some modifications as previously described [48]. Briefly, 96-well polystyrene plates (PolySorp, Nunc, Denmark) were coated with NeuGcGM3 PIK3C2G or NeuAcGM3 at a saturating concentration of 200 ng/well in methanol. Plates were allowed to dry for 2 h at 37°C and then blocked with 4% human serum albumin in PBS for 2 h at 4°C. Control wells, coated only with methanol, were equally treated with blocking solution. Diluted human sera (1/50 in PBS-0.4% human serum albumin) were added to the wells and incubated overnight at 4°C. The plates were washed six times with PBS containing 0.1% Tween 20 (PBST) and then incubated with biotin-conjugated goat antihuman IgG + IgM (Jackson ImmunoResearch Laboratories, Inc, West Grove, PA, USA) for 1.5 h at RT. After washing in the same conditions, alkaline phosphatase conjugated streptavidin (Jackson ImmunoResearch Laboratories) was added and incubated for an additional 1.5 h at RT. Finally, a substrate solution consisting of 1 mg/mL p-nitrophenylphosphate in diethanolamine buffer, pH 9.8, was added to the plates and the absorbance was measured at 405 nm in an ELISA reader (Organon Teknika, Salsburg, Austria). To consider that a serum sample had a positive reaction to a particular ganglioside, values of absorbance had to be ≥0.