Klein E, Masucci M G, Masucci G, Vánky F
Mol Immunol. 1982 Oct;19(10):1323-9. doi: 10.1016/0161-5890(82)90300-5.
Natural killer (NK) activity is an operational designation. It implies the in vitro cytotoxicities registered in short-term tests exerted by lymphocytes derived from donors with no known immunization history against the particular target. The strength of the effect exerted by unmanipulated blood lymphocytes shows an individual variation. Short-term in vitro treatment with interferon elevates the lytic potential of lymphocytes. Owing to the heterogeneity of the cytotoxic blood lymphocytes with regard of cell surface properties it is not possible to separate all active cells and inactive cells in clean populations. A considerable enrichment of active cells can be achieved if nylon wool non-adherent, large, granular Fc gamma receptor positive SRBC receptor negative--or low-avidity SRBC receptor positive--OKM1-reactive cells are separated. Negative cells are concentrated in the Fc receptor and OKM1-negative high-avidity SRBC receptor positive high cell density subset. The activity of lymphocytes in the former category is potentiated by interferon and the latter acquire the lytic function if PHA is added to the assay system. Freshly separated, non-cultured tumor cells are not or weakly sensitive to the effect of unmanipulated lymphocytes. However, when the lymphocytes are treated with interferon prior to the assay a lytic potential can be induced even against these in allogeneic effector target combinations. Cytotoxic cells which acquired the function after in vivo and/or in vitro immunization are designated as 'cytotoxic T-lymphocytes' (CTL), and were shown to act on the basis of antigen recognition. The expression of known T-markers on at least a fraction of the active cells and the recognition of alloantigens in NK systems suggest that the distinction between CTL and NK cells is not as sharp as initially suggested.
自然杀伤(NK)活性是一种操作性定义。它意味着在短期试验中所记录的体外细胞毒性,这些试验由来自无针对特定靶标的已知免疫史供体的淋巴细胞进行。未经处理的血液淋巴细胞所发挥作用的强度表现出个体差异。用干扰素进行短期体外处理可提高淋巴细胞的裂解潜能。由于细胞毒性血液淋巴细胞在细胞表面特性方面存在异质性,因此不可能在纯净群体中分离出所有活性细胞和非活性细胞。如果分离出尼龙毛非黏附、大颗粒、Fcγ受体阳性、SRBC受体阴性——或低亲和力SRBC受体阳性——OKM1反应性细胞,就可以实现活性细胞的大量富集。阴性细胞集中在Fc受体和OKM1阴性、高亲和力SRBC受体阳性、高细胞密度亚群中。前一类淋巴细胞的活性可被干扰素增强,而后一类淋巴细胞如果在检测系统中加入PHA则可获得裂解功能。新鲜分离的、未培养的肿瘤细胞对未经处理的淋巴细胞的作用不敏感或仅有微弱敏感性。然而,当在检测前用干扰素处理淋巴细胞时,即使在同种异体效应细胞 - 靶细胞组合中,也可诱导出针对这些肿瘤细胞的裂解潜能。在体内和/或体外免疫后获得功能的细胞毒性细胞被称为“细胞毒性T淋巴细胞”(CTL),并且已证明它们基于抗原识别发挥作用。至少一部分活性细胞上已知T标记的表达以及NK系统中同种异体抗原的识别表明,CTL和NK细胞之间的区别并不像最初认为的那样明显。