Monson J R, Ramsden C, Guillou P J
Br J Surg. 1986 Jun;73(6):483-6. doi: 10.1002/bjs.1800730620.
Mitogen-stimulated basal and maximal interleukin-2 production has been measured in 60 control subjects and 45 patients with gastrointestinal cancer (14 localized and 31 advanced). Peripheral blood T cell subsets in these subjects were also measured. In patients with advanced gastrointestinal cancer interleukin-2 production (mean +/- s.e.m. units/ml) is impaired when compared with that of control subjects (26.5 +/- 7 versus 61.1 +/- 9, P less than 0.0001) or patients with localized cancer (26.5 +/- 7 versus 59.4 +/- 13, P less than 0.02). This cannot be restored to normal by in vitro irradiation of the lymphocytes, suggesting that the impaired function is not due to IL-2 suppressor cells. Using monoclonal antibodies the percentages of T cell subsets were similar in all groups and we therefore conclude that the reduced production of IL-2 in these patients is due to deficient helper T cell function. These results provide a rational basis for the administration of exogenous IL-2 in the future management of patients with advanced gastrointestinal cancer.
在60名对照受试者和45例胃肠癌患者(14例局限性癌和31例进展期癌)中,检测了丝裂原刺激下白细胞介素-2的基础分泌量和最大分泌量。还对这些受试者的外周血T细胞亚群进行了检测。与对照受试者(26.5±7对61.1±9,P<0.0001)或局限性癌患者(26.5±7对59.4±13,P<0.02)相比,进展期胃肠癌患者的白细胞介素-2分泌量(平均±标准误,单位/ml)受损。淋巴细胞的体外照射不能使其恢复正常,这表明功能受损并非由于白细胞介素-2抑制细胞所致。使用单克隆抗体检测发现,所有组的T细胞亚群百分比相似,因此我们得出结论,这些患者白细胞介素-2分泌减少是由于辅助性T细胞功能缺陷所致。这些结果为未来进展期胃肠癌患者的外源性白细胞介素-2给药提供了合理依据。