Crispino S, Lissoni P, Ardizzoia A, Rovelli F, Perego M S, Grassi M G, Barni S, Pittalis S, Tancini G
Division of Radiation Oncology, San Gerardo Hospital, Monza, (MI), Italy.
J Biol Regul Homeost Agents. 1993 Jul-Sep;7(3):92-4.
SIL-2R levels mainly depend on a T lymphocyte production. The mechanisms responsible for the elevated blood concentrations of SIL-2R in advanced solid tumors are still unknown. To investigate the role played by the monocyte-macrophage system on SIL-2R release, we have evaluated serum levels of SIL-2R in 10 head and neck cancer patients during GM-CSF subcutaneous administration (3 mcg/kg/day for 11 consecutive days). Serum levels of TNF and neopterin, both produced by macrophages, were also measured. SIL-2R mean concentration significantly enhanced in response to GM-CSF, and their rise positively correlated to that in TNF and neopterin values, while lymphocyte mean number did not increase during the study. The present results represent the first in vivo demonstration that SIL-2R release is related to macrophage activation, rather than to depend only on lymphocyte proliferation.
可溶性白细胞介素-2受体(SIL-2R)水平主要取决于T淋巴细胞的产生。晚期实体瘤患者血液中SIL-2R浓度升高的机制尚不清楚。为了研究单核细胞-巨噬细胞系统在SIL-2R释放中所起的作用,我们评估了10例头颈部癌患者在皮下注射粒细胞-巨噬细胞集落刺激因子(GM-CSF,3微克/千克/天,连续11天)期间血清中SIL-2R的水平。同时还检测了巨噬细胞产生的肿瘤坏死因子(TNF)和新蝶呤的血清水平。GM-CSF刺激后,SIL-2R的平均浓度显著升高,其升高与TNF和新蝶呤值的升高呈正相关,而研究期间淋巴细胞的平均数量没有增加。目前的结果首次在体内证明,SIL-2R的释放与巨噬细胞激活有关,而不仅仅取决于淋巴细胞增殖。