Alvarado C S, Findley H W, Chan W C, Hnath R S, Abdel-Mageed A, Pais R C, Kutner M H, Ragab A H
Department of Pediatrics, Emory University School of Medicine, Atlanta, Georgia 30322.
Cancer. 1989 Jan 1;63(1):83-9. doi: 10.1002/1097-0142(19890101)63:1<83::aid-cncr2820630114>3.0.co;2-a.
Natural killer (NK) cells and NK cell activity were determined in three groups (newly diagnosed [n = 21], on therapy [n = 21], and off therapy [n = 18]) of children with various types of malignant solid tumors and in a control group (n = 26) by means of Leu-7 and Leu-11b monoclonal antibodies and a 4-hour 51Cr-release assay, respectively. The erythroleukemia cell line K562 was used as a target cell. The newly diagnosed group included eight patients with localized disease (Stage I-II), ten with bulky but nonmetastatic disease (Stage III), and three with metastases (Stage IV). The mean percent of NK cell activity in the newly diagnosed group was significantly higher than that of the control group. Children with Stage III tumors at diagnosis had higher mean NK cell function than those with Stage I-II and Stage IV. On therapy patients had significantly fewer NK cells and lower NK cell cytotoxicity than those in the other groups studied. We also studied the following: (1) the in vitro effect of recombinant interferon-alpha (rIFN-alpha) and recombinant interleukin-2 (rIL-2) on NK cell function of peripheral blood lymphocytes (PBL) from children with solid malignancies; and (2) the susceptibility of neuroblastoma-derived (CHP-126 and SKNSH) and rhabdomyosarcoma-derived (A-204) cell lines to NK cell lysis. Both rIFN-alpha and rIL-2 enhanced NK cell activity of PBL from children with malignancies and healthy children against K562 and solid tumor cell lines. The enhancing effect or rIL-2 was greater than that of rIFN-alpha. CHP-126 and SKNSH cell lines were susceptible to NK cell lysis mediated by the PBL of children with neuroblastoma and the control group. The A-204 cell line was less sensitive than K562 to NK cell cytotoxicity. Our results suggest a potential therapeutic role for both cytokines in the treatment of malignant solid tumors of childhood.
采用Leu - 7和Leu - 11b单克隆抗体以及4小时51Cr释放试验,分别测定了三组患有各种类型恶性实体瘤的儿童(新诊断组[n = 21]、治疗组[n = 21]和治疗结束组[n = 18])以及一个对照组(n = 26)的自然杀伤(NK)细胞和NK细胞活性。红白血病细胞系K562用作靶细胞。新诊断组包括8例局限性疾病(I - II期)患者、10例肿块较大但无转移疾病(III期)患者和3例有转移患者(IV期)。新诊断组NK细胞活性的平均百分比显著高于对照组。诊断时为III期肿瘤的儿童,其平均NK细胞功能高于I - II期和IV期的儿童。治疗组患者的NK细胞明显少于其他研究组,且NK细胞细胞毒性较低。我们还研究了以下内容:(1)重组干扰素 - α(rIFN - α)和重组白细胞介素 - 2(rIL - 2)对实体恶性肿瘤患儿外周血淋巴细胞(PBL)NK细胞功能的体外影响;(2)神经母细胞瘤来源的(CHP - 126和SKNSH)和横纹肌肉瘤来源的(A - 204)细胞系对NK细胞裂解的敏感性。rIFN - α和rIL - 2均增强了恶性肿瘤患儿和健康儿童的PBL对K562和实体瘤细胞系的NK细胞活性。rIL - 2的增强作用大于rIFN - α。CHP - 126和SKNSH细胞系对神经母细胞瘤患儿和对照组的PBL介导的NK细胞裂解敏感。A - 204细胞系对NK细胞细胞毒性的敏感性低于K562。我们的结果表明,这两种细胞因子在儿童恶性实体瘤的治疗中具有潜在的治疗作用。