Richter M, Banerjee D, Sklar S
Immunology. 1981 Sep;44(1):109-18.
The naturally-occurring antibody-independent cellular cytotoxic activity (NOCC) of normal circulating human monocytes and neutrophils was investigated employing a number of erythrocytes and the K-562 cell line as target cells simultaneously. The identity of the effector cell(s) was shown to be dependent upon or be a function of the type of target cell selected for the assay system. A number of erythrocyte targets (rabbit, horse, sheep and ox erythrocytes) were lysed to varying degrees by neutrophils and monocytes and not by lymphocytes. Irrespective of the red blood cell (RBC) target, the effector monocyte invariably possessed receptors for both C'3 and the Fc of IgG. In contrast, the cytotoxic cells using the K-562 target cell were lymphocytes. Monocytes and neutrophils were inactive. The cytotoxic-enhancing activity in normal human serum exhibits specific and non-specific properties which suggests that more than one factor is involved. With respect to the monocyte cytotoxic cells, only the rabbit erythrocytes could totally absorb the serum factor in a specific fashion. Absorption of the serum with horse, sheep or ox erythrocytes resulted in a significant loss of potentiating activity with respect to all of the erythrocyte targets but a more marked loss of activity using the absorbing erythrocytes as targets. With respect to the polymorphonuclear leucocyte effector cells, only the rabbit RBC were capable of specifically absorbing out the cytotoxic-enhancing factor present in the normal human serum. Absorption of the serum with sheep, horse or ox RBC resulted in total cross-absorption of the enhancing factor. Chicken and human RBC, which do not serve as targets for the NOCC assay, could not absorb out the cytotoxic-enhancing factor with respect to any of the target erythrocytes. The composition of the soluble serum factor(s) is under current investigation but it is not an immunoglobulin since pure serum albumin can substitute for normal serum in the NOCC assay. The mechanism of erythrocyte lysis by the cytotoxic monocyte was investigated. Mononuclear cells were incubated with target cell monolayers and with target cells under optimal rosetting conditions. No interaction between the effector and target cells could be detected. The monocytes did not adhere to the target cell monolayer nor did they form rosettes with the target cells. Thus, the results fail to corroborate or support the assumption that the cytotoxic activity of the monocyte is dependent upon conventionally-detectable receptors. Erythrophagocytosis was not observed to any significant degree under the assay conditions used. Therefore, the nature of the interaction between the cytotoxic monocyte and the erythroid target cell which results in lysis of the target cell remains to be elucidated.
同时使用多种红细胞和K-562细胞系作为靶细胞,对正常循环的人单核细胞和中性粒细胞的天然存在的非抗体依赖性细胞毒性活性(NOCC)进行了研究。结果表明,效应细胞的身份取决于或与为检测系统选择的靶细胞类型有关。多种红细胞靶标(兔、马、绵羊和牛红细胞)被中性粒细胞和单核细胞不同程度地裂解,而淋巴细胞则不能。无论红细胞(RBC)靶标如何,效应单核细胞始终具有C'3和IgG的Fc的受体。相比之下,使用K-562靶细胞的细胞毒性细胞是淋巴细胞。单核细胞和中性粒细胞无活性。正常人血清中的细胞毒性增强活性表现出特异性和非特异性特性,这表明涉及不止一种因素。对于单核细胞毒性细胞,只有兔红细胞能够以特异性方式完全吸收血清因子。用马、绵羊或牛红细胞吸收血清会导致所有红细胞靶标的增强活性显著丧失,但以吸收红细胞作为靶标时活性丧失更明显。对于多形核白细胞效应细胞,只有兔红细胞能够特异性吸收正常人血清中存在的细胞毒性增强因子。用绵羊、马或牛红细胞吸收血清会导致增强因子的完全交叉吸收。鸡和人红细胞不作为NOCC检测的靶标,不能吸收任何靶红细胞的细胞毒性增强因子。目前正在研究可溶性血清因子的组成,但它不是免疫球蛋白,因为纯血清白蛋白可以在NOCC检测中替代正常血清。研究了细胞毒性单核细胞裂解红细胞的机制。将单核细胞与靶细胞单层以及在最佳玫瑰花结形成条件下的靶细胞一起孵育。未检测到效应细胞与靶细胞之间的相互作用。单核细胞既不粘附于靶细胞单层,也不与靶细胞形成玫瑰花结。因此,结果未能证实或支持单核细胞的细胞毒性活性取决于传统可检测受体的假设。在所使用的检测条件下,未观察到明显程度的红细胞吞噬作用。因此,导致靶细胞裂解的细胞毒性单核细胞与红细胞靶细胞之间相互作用的性质仍有待阐明。