Wanebo H J, Riley T, Katz D, Pace R C, Johns M E, Cantrell R W
Department of Surgery, University of Virginia Medical Center, Charlottesville.
Cancer. 1988 Feb 1;61(3):462-74. doi: 10.1002/1097-0142(19880201)61:3<462::aid-cncr2820610310>3.0.co;2-z.
Head and neck cancer (H&N CA) patients have known depression of cell-mediated immunity. There is suggestive evidence that prostaglandin (PGE2)-secreting cells may be a major factor. The authors have sought to determine the role of PGE2-releasing monocytes-macrophages in this immune depression by determining the effects of adherent cell depletion and by measuring the effects of indomethacin, a PGE2 synthetase inhibitor, on selected tests of lymphocyte function. Lymphocyte stimulation with phytohemagglutinin (PHA) (T-cell stimulant) and Staph phage lysate (SPL) (B-cell stimulant) was done in the presence of varying concentrations of indomethacin; the effect of adherent cell depletion also was determined. The study population included 45 patients with localized or locoregional squamous CA of the H&N and 40 controls. Results included the following: (1) lymphocyte stimulation responses to PHA and SPL were generally depressed in the CA patients versus controls; (2) incubation with indomethacin produced bivalent effects in both controls and CA patients, depending on the concentration of indomethacin and lymphocyte stimulant; incubation with optimum concentrations of indomethacin generally produced augmented responses in both study groups whereas high concentrations of indomethacin were suppressive; (3) the immune potentiating effects were not observed in older patients with advanced disease; and (4) removal of adherent leukocytes (mainly monocytes) also restored depressed lymphocyte responses. Although other factors also are operative, our data suggest that PGE2-secreting monocytes-macrophages may have a major role in the immune depression of H&N CA patients. Age and host effects of the cancer and the malnutrition common to these patients probably are involved also, although their singular contribution has not been measured. This depression is largely reversible by a PGE2 synthesis inhibitor, indomethacin, which suggests the potential value of in vivo administration of indomethacin to H&N CA patients as an adjunct.
头颈癌(H&N CA)患者存在细胞介导免疫功能下降的情况。有证据表明,分泌前列腺素(PGE2)的细胞可能是一个主要因素。作者试图通过确定贴壁细胞耗竭的影响以及测量PGE2合成酶抑制剂吲哚美辛对选定淋巴细胞功能测试的影响,来确定释放PGE2的单核细胞-巨噬细胞在这种免疫抑制中的作用。在不同浓度的吲哚美辛存在下,用植物血凝素(PHA)(T细胞刺激剂)和葡萄球菌噬菌体裂解物(SPL)(B细胞刺激剂)刺激淋巴细胞;还确定了贴壁细胞耗竭的影响。研究人群包括45例局部或局部区域鳞状头颈癌患者和40例对照。结果如下:(1)与对照组相比,癌症患者对PHA和SPL的淋巴细胞刺激反应普遍降低;(2)与吲哚美辛孵育在对照组和癌症患者中产生了双向效应,这取决于吲哚美辛和淋巴细胞刺激剂的浓度;与最佳浓度的吲哚美辛孵育通常在两个研究组中都产生增强的反应,而高浓度的吲哚美辛则具有抑制作用;(3)在老年晚期疾病患者中未观察到免疫增强作用;(4)去除贴壁白细胞(主要是单核细胞)也恢复了降低的淋巴细胞反应。尽管其他因素也起作用,但我们的数据表明,分泌PGE2的单核细胞-巨噬细胞可能在头颈癌患者的免疫抑制中起主要作用。这些患者常见的癌症年龄和宿主效应以及营养不良可能也有涉及,尽管它们的单独作用尚未测量。这种抑制作用在很大程度上可被PGE2合成抑制剂吲哚美辛逆转,这表明对头颈癌患者体内给予吲哚美辛作为辅助治疗具有潜在价值。