1986
DOI: 10.1016/0145-2126(86)90043-3
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Natural and antibody-dependent cellular cytotoxicity in chronic myeloid leukemia patients in remission

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Cited by 10 publications
(16 citation statements)
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“…As reported earlier [9] and given in table I, when antibody-coated CRBCs were used as targets, there was no significant difference between the ADCC activ ity of healthy donors and CML low NK responders although the latter showed somewhat reduced cyto toxicity. However, when K562 coated with MAb 4.6E10 were used as targets, the ADCC activity was significantly lower in normal as well as low NK re sponder CML patients (table I).…”
Section: Adcc Activity O F Napbm Nc From Healthy Donors and CM L Patimentioning
confidence: 64%
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“…As reported earlier [9] and given in table I, when antibody-coated CRBCs were used as targets, there was no significant difference between the ADCC activ ity of healthy donors and CML low NK responders although the latter showed somewhat reduced cyto toxicity. However, when K562 coated with MAb 4.6E10 were used as targets, the ADCC activity was significantly lower in normal as well as low NK re sponder CML patients (table I).…”
Section: Adcc Activity O F Napbm Nc From Healthy Donors and CM L Patimentioning
confidence: 64%
“…Effector cells cultured at the same density in CM without IL-2 or IFN served as controls in all the experiments. For NK cytotoxicity a 4-hour 51Cr release assay was performed as described earlier [9]. MAh 10 pi culture supernatant containing theanti-K562 MAb 4.6E10 was added to 104 51Cr-labcllcd K562 cells in 100 pi of CM.…”
Section: Separation Anti Treatment O F Effector Cells With Ifn and Il-2mentioning
confidence: 99%
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“…The NK and LAK cell activities were determined using the standard four-hour 5"Chromium release assay (Dabholkar et al, 1986;Tatake et al, 1989). The NK-sensitive targets used were K562 cells.…”
Section: Cytotoxicity Assay and Targetsmentioning
confidence: 99%
“…The frequency of LAK cell precursors has also been studied using limiting dilution analysis (LDA Separation of lymphocytes PBL were separated on Ficoll-Hypaque (FH) gradient (Pharmacia, Sweden). The non-adherent PBL were obtained to assess NK activity as described before (Dabholkar et al, 1986). LAK cells were generated from the total PBL population using the predetermined optimum dose of 10 u recombinant IL-2 (rIL-2, Biogen, S.A., Switzerland) per 1 x 106 lymphocytes (Tatake et al, 1989).…”
mentioning
confidence: 99%