Soucek J, Hilgert I, Budová I, Lindnerová G
Institute of Hematology and Blood Transfusion, Prague, Czech Republic.
Neoplasma. 1994;41(2):75-81.
The aim of the present study was to induce NK cell activity in peripheral mononuclear cells (PMNC) of normal individuals or of leukemic patients. For this purpose, monoclonal antibodies (mAbs) anti-CD3 (MEM 57, OKT 3 and MEM 92), anti-CD59 (MEM 43) and anti-CD43 (MEM 59) were tested. MEM 43, MEM 59, MEM 57 and OKT 3 stimulated markedly the NK activity in fresh isolated PMNC of normal individuals, whereas the cytotoxicity in 3-day cultivated PMNC was enhanced only by MEM 57 and OKT 3. In comparison to interleukin-2 (IL-2), MEM 57 and OKT 3 induced less PMNC cytotoxicity but more cell proliferation. MEM 92 (anti-CD3, IgM) compared to MEM 57 or OKT 3 (anti-CD3, IgG) did not show any effect on both reactions mentioned above. PMNC of untreated leukemic patients exerted very negligible NK cell activity. Following 3-day culture of leukemic PMNC with OKT 3 or IL-2 the anti-K 562 cytotoxicity was markedly enhanced. In some cases the stimulating effect was more pronounced by IL-2, in others by OKT 3. Nevertheless, the best effect was gained in 7 out of 12 patients using a combination of IL-2 and OKT 3. On the other hand, OKT 3 did not synergize with IL-2 in normal PMNC culture.
本研究的目的是诱导正常个体或白血病患者外周血单个核细胞(PMNC)中的NK细胞活性。为此,测试了抗CD3单克隆抗体(mAb,MEM 57、OKT 3和MEM 92)、抗CD59(MEM 43)和抗CD43(MEM 59)。MEM 43、MEM 59、MEM 57和OKT 3显著刺激正常个体新鲜分离的PMNC中的NK活性,而仅MEM 57和OKT 3可增强培养3天的PMNC的细胞毒性。与白细胞介素-2(IL-2)相比,MEM 57和OKT 3诱导的PMNC细胞毒性较小,但细胞增殖较多。与MEM 57或OKT 3(抗CD3,IgG)相比,MEM 92(抗CD3,IgM)对上述两种反应均无任何影响。未经治疗的白血病患者的PMNC表现出非常微弱的NK细胞活性。用OKT 3或IL-2对白血病PMNC进行3天培养后,抗K 562细胞毒性显著增强。在某些情况下,IL-2的刺激作用更明显,在其他情况下,OKT 3的刺激作用更明显。然而,12例患者中有7例使用IL-2和OKT 3联合使用时效果最佳。另一方面,在正常PMNC培养中,OKT 3与IL-2没有协同作用。