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热疗对自然细胞介导的细胞毒性的体外效应。

In vitro effect of hyperthermia on natural cell-mediated cytotoxicity.

作者信息

Fuggetta M P, Alvino E, Tricarico M, D'Atri S, Pepponi R, Prete S P, Bonmassar E

机构信息

Institute of Experimental Medicine, CNR, Rome, Italy.

出版信息

Anticancer Res. 2000 May-Jun;20(3A):1667-72.

Abstract

It is well known that hyperthermia (HY), which is used for the treatment of cancer, depresses natural cell-mediated immunity in vitro. Experiments were performed to confirm the inhibitory effect of HY (42 degrees C for 1 hour) on natural killer (NK) activity and to evaluate the influence of HY on the generation and cytotoxic activity of interleukin-2 (IL-2)-activated NK cells. Additional experiments were also carried out to evaluate the effect of a simultaneous exposure of effector and target cells to HY. The results showed that HY profoundly reduced the lytic activity of NK cells and demonstrated that this inhibition was transient and not due to an apoptosis-induced reduction of the number of effector cells. Moreover, the exposure of mononuclear cells to HY before IL-2 stimulation did not affect the generation of IL-2-activated NK cells, whereas, the hyperthermic treatment of IL-2-activated NK cells produced a marked reduction of their cytotoxic activity. The results also showed that the simultaneous exposure of effector and target cells to HY, during the cytotoxicity assay, produced a marked reduction of lytic activity of NK and IL-2-activated NK cells, and that this impairment was specific for effector cells. In this context, heat-exposure of target cells alone, did not substantially modify their susceptibility to lysis induced by either NK or IL-2-activated NK cells. These results add further evidence of HY-induced inhibition of natural cell-mediated immunity, and suggest that, in the course of therapeutic HY, immune response could be significantly altered.

摘要

众所周知,用于癌症治疗的热疗(HY)在体外会抑制天然细胞介导的免疫。进行实验以证实热疗(42摄氏度,持续1小时)对自然杀伤(NK)活性的抑制作用,并评估热疗对白细胞介素-2(IL-2)激活的NK细胞的生成和细胞毒性活性的影响。还进行了额外的实验以评估效应细胞和靶细胞同时暴露于热疗的效果。结果表明,热疗显著降低了NK细胞的裂解活性,并表明这种抑制是短暂的,并非由于凋亡导致效应细胞数量减少。此外,在IL-2刺激前将单核细胞暴露于热疗并不影响IL-2激活的NK细胞的生成,而对IL-2激活的NK细胞进行热疗则使其细胞毒性活性显著降低。结果还表明,在细胞毒性测定过程中,效应细胞和靶细胞同时暴露于热疗会导致NK细胞和IL-2激活的NK细胞的裂解活性显著降低,且这种损伤对效应细胞具有特异性。在这种情况下,仅对靶细胞进行热暴露并不会显著改变它们对NK细胞或IL-2激活的NK细胞诱导裂解的敏感性。这些结果进一步证明了热疗诱导的对天然细胞介导免疫的抑制作用,并表明在治疗性热疗过程中,免疫反应可能会发生显著改变。

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