Huddlestone J R, Merigan T C, Oldstone M B
Nature. 1979 Nov 22;282(5737):417-9. doi: 10.1038/282417a0.
Natural killer (NK) cells are non-B, non-T lymphocytes that effect spontaneous cytolysis of both virus-infected and neoplastically transformed target cells. These NK lymphocytes have been detected in several species including man. Interferon is a primary regulator of natural killer activity. Because NK cells have been implicated in the regulation of tumour cell expression and can be induced by interferon in murine models, we have studied patients receiving large doses of interferon to determine (1) whether interferon could induce NK lymphocytes in the peripheral blood of man, and (2) whether there are characteristic kinetics for the appearance, disappearance and reactivation of NK lymphocytes following interferon therapy. We report here the activation of human NK cells by the systemic inoculation of human subjects with interferon. Five patients received interferon as therapy for non-Hodgkin's lymphoma. All showed a marked increase in NK cell activity 12--24 h after inoculation. Peak NK activity occurred 18 h after introducing interferon, and thereafter declined rapidly but remained above pre-interferon levels. Induced NK activity occurred with reintroduction of interferon but at lower levels of activity and with different kinetics.
自然杀伤(NK)细胞是一种非B、非T淋巴细胞,可对病毒感染细胞和肿瘤转化细胞进行自发细胞溶解。这些NK淋巴细胞已在包括人类在内的多种物种中被检测到。干扰素是自然杀伤活性的主要调节因子。由于NK细胞与肿瘤细胞表达的调节有关,并且在小鼠模型中可被干扰素诱导,我们研究了接受大剂量干扰素治疗的患者,以确定:(1)干扰素是否能在人类外周血中诱导NK淋巴细胞;(2)干扰素治疗后NK淋巴细胞的出现、消失和重新激活是否具有特征性动力学。我们在此报告通过给人类受试者全身接种干扰素来激活人NK细胞的情况。五名患者接受干扰素治疗非霍奇金淋巴瘤。接种后12至24小时,所有患者的NK细胞活性均显著增加。引入干扰素后18小时出现NK活性峰值,此后迅速下降,但仍高于干扰素治疗前水平。再次引入干扰素时会诱导NK活性,但活性水平较低且动力学不同。