Lundgren G, Möller G
Clin Exp Immunol. 1969 Apr;4(4):435-52.
The cytotoxic effect of non-immunized human lymphocytes was investigated in a system where the lymphocytes were applied to fibroblast monolayers of different genotypes. Non-immunized lymphocytes were not cytotoxic, disregarding the target cell genotype provided that the lymphocyte suspensions were free from contaminating granulocytes. By adding phytohaemagglutinin (PHA) to the culture, the lymphocytes became strongly cytotoxic and exerted their effect already after 4–8 hr. Cytotoxicity was shown to develop independently of other expressions of PHA-stimulation of the lymphocyte, such as RNA-, protein- and DNA-syntheses and morphological transformation. Living lymphocytes were required for cytotoxicity to occur and heating the lymphocytes to 48·5°C, ultrasound disintegration or freezing-thawing abolished their ability to damage the target cells. The PHA-induced cytotoxicity was equally expressed on allogeneic and autochthonous fibroblasts. Analogous results were obtained when the lymphocytes were stimulated by streptolysin O or anti-lymphocyte serum. The results suggest that expression of cytotoxicity is an immunologically non-specific process, caused by stimulated lymphocytes. When the lymphocytes have acquired a cytotoxic potential they do not discriminate between the target cell genotype or the event triggering lymphocyte cytotoxicity. The specificity of the cellular immune reactions is probably confined to the immunological recognition step initiating the cytotoxic potential. This recognition step is by-passed if the lymphocytes are stimulated by PHA or other non-specific stimulators.
在一个将淋巴细胞应用于不同基因型成纤维细胞单层的系统中,研究了未免疫的人淋巴细胞的细胞毒性作用。只要淋巴细胞悬液中没有污染的粒细胞,未免疫的淋巴细胞就没有细胞毒性,而与靶细胞基因型无关。通过向培养物中添加植物血凝素(PHA),淋巴细胞变得具有强烈的细胞毒性,并且在4-8小时后就开始发挥作用。结果表明,细胞毒性的发展与PHA刺激淋巴细胞的其他表现无关,如RNA、蛋白质和DNA的合成以及形态转化。细胞毒性的发生需要活的淋巴细胞,将淋巴细胞加热到48.5°C、超声破碎或冻融都会消除它们损伤靶细胞的能力。PHA诱导的细胞毒性在同种异体和自体成纤维细胞上均有同等程度的表达。当淋巴细胞受到链球菌溶血素O或抗淋巴细胞血清刺激时,也获得了类似的结果。这些结果表明,细胞毒性的表达是一个由受刺激淋巴细胞引起的免疫非特异性过程。当淋巴细胞获得细胞毒性潜能时,它们不会区分靶细胞基因型或触发淋巴细胞细胞毒性的事件。细胞免疫反应的特异性可能仅限于启动细胞毒性潜能的免疫识别步骤。如果淋巴细胞受到PHA或其他非特异性刺激物的刺激,这个识别步骤就会被绕过。