Holm G, Perlmann P
Immunology. 1967 May;12(5):525-36.
The cytotoxic effect of normal human blood lymphocytes on Chang cells in tissue culture was investigated. Cell damage was measured by release of Cr from pre-labelled tissue culture `target' cells. This method was sensitive and rendered highly reproducible results. Released Cr was not re-utilized. About 25 per cent of the Cr was spontaneously released from labelled Chang cells when incubated for 24 hours at 37°. Lymphocytes at a lymphocyte/Chang cell ratio of 25:1 led to a slight increase of this release. When phytohaemagglutinin was also present, about 50–60 per cent of the isotope appeared in the medium. Under these conditions target cells were significantly damaged within 1 hour. At a lymphocyte/Chang cell ratio of only 1:1, weak cytotoxic effects were also noted after 24 hours of incubation. The results of dose—response experiments suggested that a considerable proportion of the lymphocytes participated in the reaction. Individual variation of the cytotoxic effect of lymphocytes from different donors suggested that it could be related to the degree of histoincompatibility between lymphocytes and Chang cells. Under the present conditions contaminating erythrocytes or granulocytes did not interfere with the cytotoxic action of the lymphocytes.
研究了正常人血液淋巴细胞对组织培养中的Chang细胞的细胞毒性作用。通过预先标记的组织培养“靶”细胞释放铬来测量细胞损伤。该方法灵敏,结果高度可重复。释放出的铬未被再利用。当在37°孵育24小时时,约25%的铬从标记的Chang细胞中自发释放。淋巴细胞与Chang细胞比例为25:1时,这种释放略有增加。当同时存在植物血凝素时,约50 - 60%的同位素出现在培养基中。在这些条件下,靶细胞在1小时内受到显著损伤。淋巴细胞与Chang细胞比例仅为1:1时,孵育24小时后也观察到微弱的细胞毒性作用。剂量反应实验结果表明,相当一部分淋巴细胞参与了反应。来自不同供体的淋巴细胞细胞毒性作用的个体差异表明,这可能与淋巴细胞和Chang细胞之间的组织不相容程度有关。在目前条件下,污染的红细胞或粒细胞不干扰淋巴细胞的细胞毒性作用。