Haukaas S, Høisaeter P A, Kalland T
Prostate. 1982;3(4):405-14. doi: 10.1002/pros.2990030410.
The responsiveness to diethylstilbestrol (DES) and estramustinephosphate (EMP) of human peripheral blood lymphocytes to T-cell mitogens has been investigated in vitro and in vivo. EMP demonstrated potent inhibition of both Con A- and PHA-induced lymphocyte proliferation in vitro, while it had no detectable effects when given to patients with cancer of the prostate. DES reduced the response to Con A in vitro, but had only marginal effects on PHA-induced mitogen response. In contrast, the response to Con A was unaltered, while the response to PHA was significantly diminished after DES therapy in patients with prostatic cancer. This effect, however, was only seen when high doses of DES not included in conventional regimen were given. The proliferative response to T-cell mitogens in patients with prostatic cancer was not affected by serum source in the assay, indicating the absence of humoral factors able to inhibit mitogen response in these patients.
已在体外和体内研究了人外周血淋巴细胞对己烯雌酚(DES)和磷酸雌莫司汀(EMP)对T细胞有丝分裂原的反应性。EMP在体外对刀豆蛋白A(Con A)和植物血凝素(PHA)诱导的淋巴细胞增殖均显示出强效抑制作用,而给予前列腺癌患者时则未检测到其效果。DES在体外降低了对Con A的反应,但对PHA诱导的有丝分裂原反应仅有轻微影响。相比之下,前列腺癌患者接受DES治疗后,对Con A的反应未改变,而对PHA的反应则显著减弱。然而,这种效应仅在给予常规方案中未包含的高剂量DES时才会出现。前列腺癌患者对T细胞有丝分裂原的增殖反应不受检测中血清来源的影响,表明这些患者不存在能够抑制有丝分裂原反应的体液因子。