Kurzrock R, Redman J, Cabanillas F, Jones D, Rothberg J, Talpaz M
Department of Medical Oncology, University of Texas M. D. Anderson Cancer Center, Houston 77030.
Cancer Res. 1993 May 1;53(9):2118-22.
Several cytokines including gamma-interferon, tumor necrosis factor alpha, interleukin 1 beta (IL-1 beta), and interleukin 6 (IL-6) are pyrogenic and can inhibit lipogenic processes. Because patients with lymphoma often suffer from fever, weight loss, and night sweats (B symptoms), the etiology of which is unknown, the authors investigated serum levels of these cytokines in normal volunteers and in patients with Hodgkin's and non-Hodgkin's lymphoma. Sixty serum samples from patients with Hodgkin's disease (28 patients) or non-Hodgkin's lymphoma (32 patients), as well as 20 samples from normal volunteers, were collected. The majority of patients had advanced (Stage III or IV) or relapsed disease. The assay for gamma-interferon was a specific and sensitive radioimmunoassay (lower limit of detection = 0.1 unit/ml); the assays for tumor necrosis factor alpha, IL-1 beta, and IL-6 were enzyme-linked immunoassays with lower limits of sensitivity of 10 pg/ml, 20 pg/ml, and 22 pg/ml, respectively. There were no statistically significant differences in gamma-interferon, tumor necrosis factor alpha, or IL-1 beta levels between lymphoma patients and normal subjects. In contrast, 20 of 57 patients (35%) with lymphoma as compared with 0 of 19 normal volunteers (0%) had detectable serum IL-6 levels (P < 0.005, chi 2 test). Interestingly, 17 of 29 lymphoma patients with B symptoms (59%) as opposed to 3 of 28 lymphoma patients without B symptoms (11%) had detectable serum IL-6 levels (P < 0.001, chi 2 test); the median IL-6 level was 28.9 pg/ml (B symptoms present) versus undetectable (no B symptoms) (P < 0.005, Mann-Whitney U test). Analyzing Hodgkin's and non-Hodgkin's lymphoma groups separately revealed similar results. IL-6 levels showed no significant correlation with time from diagnosis, beta 2-microglobulin, or lactate dehydrogenase levels. However, analysis by the method of Kaplan and Meir demonstrated that the median survival of Hodgkin's disease patients with detectable IL-6 levels (> or = 22 pg/ml) was 10 mo, whereas the median survival has not been reached at a median follow-up time of 37.5 mo in those patients with lower values (Wilcoxon P value = 0.0012). There were too few patients in each subset of non-Hodgkin's lymphoma to determine the correlation between IL-6 and survival but, considered as a single group, a statistically significant correlation was not found.(ABSTRACT TRUNCATED AT 400 WORDS)
包括γ-干扰素、肿瘤坏死因子α、白细胞介素1β(IL-1β)和白细胞介素6(IL-6)在内的多种细胞因子具有致热作用,且能抑制脂肪生成过程。由于淋巴瘤患者常伴有发热、体重减轻和盗汗(B症状),但其病因不明,作者对正常志愿者以及霍奇金淋巴瘤和非霍奇金淋巴瘤患者的这些细胞因子血清水平进行了研究。收集了28例霍奇金病患者、32例非霍奇金淋巴瘤患者的60份血清样本以及20份正常志愿者的血清样本。大多数患者患有晚期(Ⅲ期或Ⅳ期)或复发疾病。γ-干扰素检测采用特异性和敏感性均较高的放射免疫分析法(检测下限=0.1单位/毫升);肿瘤坏死因子α、IL-1β和IL-6检测采用酶联免疫分析法,敏感性下限分别为10皮克/毫升、20皮克/毫升和22皮克/毫升。淋巴瘤患者与正常受试者之间的γ-干扰素、肿瘤坏死因子α或IL-1β水平无统计学显著差异。相比之下,57例淋巴瘤患者中有20例(35%)血清IL-6水平可检测到,而19例正常志愿者中无1例(0%)可检测到(P<0.005,卡方检验)。有趣的是,29例有B症状的淋巴瘤患者中有17例(59%)血清IL-6水平可检测到,而28例无B症状的淋巴瘤患者中有3例(11%)可检测到(P<0.001,卡方检验);有B症状患者的IL-6水平中位数为28.9皮克/毫升,无B症状患者则检测不到(P<0.005,曼-惠特尼U检验)。分别分析霍奇金淋巴瘤和非霍奇金淋巴瘤组得到了相似结果。IL-6水平与诊断后的时间、β2-微球蛋白或乳酸脱氢酶水平无显著相关性。然而,采用Kaplan和Meir方法分析表明,IL-6水平可检测到(≥22皮克/毫升)的霍奇金病患者的中位生存期为10个月,而IL-6水平较低的患者在中位随访时间37.5个月时仍未达到中位生存期(Wilcoxon P值=0.0012)。非霍奇金淋巴瘤各亚组患者数量过少,无法确定IL-6与生存期之间的相关性,但作为一个整体组,未发现统计学显著相关性。(摘要截断于400字)