Sørskaar D, Førre O, Stavem P
Institute of Immunology and Rheumatology, National Hospital, Oslo, Norway.
Int Arch Allergy Appl Immunol. 1988;87(2):159-64. doi: 10.1159/000234666.
Twenty-two patients with chronic lymphocytic leukemia (CLL) and 14 patients with chronic myelogenous leukemia (CML) were studied with respect to natural killer (NK) cell activity and related cell markers (Leu 7 and Leu 11b). Significantly reduced NK cell activity was detected in peripheral blood from the patients with CLL. Similarly, a reduced number of cells with the markers Leu 7 and Leu 11b (CD 16) were detected in the same patients. Removal of the leukemic cells by centrifugation of cells forming rosettes with mouse erythrocytes led to an augmented, but not fully normalized, NK activity. This indicates that the low NK activity in CLL partly may be due to overgrowth of leukemic cells. However, in spite of the lymphocytic infiltration, the NK cell activity in the bone marrow of CLL patients did not differ significantly from that of normal controls. The patients with CML in the chronic phase as well as patients in the accelerated or blast phase also had a reduced NK activity. The finding that patients in the chronic phase had a reduced NK activity and normal numbers of Leu 11b (CD 16) positive cells, together with no detectable blasts in the peripheral blood, indicates that patients with CML may have an inherent NK cell defect. The highly reduced activity found in patients with the accelerated/blast form may in addition partly be due to overgrowth of leukemic cells. This low NK activity may be of importance in the development of chronic leukemia.
对22例慢性淋巴细胞白血病(CLL)患者和14例慢性粒细胞白血病(CML)患者的自然杀伤(NK)细胞活性及相关细胞标志物(Leu 7和Leu 11b)进行了研究。在CLL患者的外周血中检测到NK细胞活性显著降低。同样,在这些患者中检测到带有Leu 7和Leu 11b(CD 16)标志物的细胞数量减少。通过用小鼠红细胞形成花环的细胞离心去除白血病细胞后,NK活性增强,但未完全恢复正常。这表明CLL中NK活性低部分可能是由于白血病细胞过度生长所致。然而,尽管存在淋巴细胞浸润,CLL患者骨髓中的NK细胞活性与正常对照相比并无显著差异。慢性期CML患者以及加速期或急变期患者的NK活性也降低。慢性期患者NK活性降低且Leu 11b(CD 16)阳性细胞数量正常,同时外周血中未检测到原始细胞,这一发现表明CML患者可能存在先天性NK细胞缺陷。加速期/急变期患者中发现的高度降低的活性可能部分还归因于白血病细胞的过度生长。这种低NK活性可能在慢性白血病的发展中具有重要意义。