Stanojević-Bakić N, Vucković-Dekić L, Milosević D, Sasić M
Institute for Oncology and Radiology of Serbia, Belgrade, Yugoslavia.
Panminerva Med. 1998 Dec;40(4):314-8.
Several studies showed that PGE-mediated immunosuppression in cancer patients may be differentially affected by conventional oncologic therapy.
Since there is little evidence about the action of immunotherapy on this suppression mechanism, we investigated the effect of therapy with a thymic agent-T-activin, on in vitro modulation of lymphoproliferative response (LPR) by indomethacin.
The results demonstrated that indomethacin added in vitro enhanced LPR in early stage melanoma patients before therapy. T-activin therapy as an adjunct to surgery improved this lymphocyte function; the post-therapy in vitro addition of indomethacin did not significantly affect mitogen response. However, in those patients whose LPR was insufficiently enhanced by immunotherapy (3/8), indomethacin had improved their lymphocyte response. In the control patient group treated by surgery alone, indomethacin significantly enhanced LPR in vitro six months after operation. Although obtained in a small number of patients, our results indicate that the enhancing effect of T-activin therapy on lymphoproliferative response may be, at least in part, due to the effect on PGE-mediated suppressor cell activity.
Furthermore, post-therapy in vitro testing may indicate a possible usefulness of this drug combination in some of the early stage melanoma patients.
多项研究表明,癌症患者中前列腺素E介导的免疫抑制可能受到传统肿瘤治疗的不同影响。
由于关于免疫疗法对这种抑制机制作用的证据很少,我们研究了胸腺因子T-激活素治疗对吲哚美辛体外调节淋巴细胞增殖反应(LPR)的影响。
结果表明,体外添加吲哚美辛可增强治疗前早期黑色素瘤患者的LPR。T-激活素治疗作为手术辅助手段可改善这种淋巴细胞功能;治疗后体外添加吲哚美辛对丝裂原反应无显著影响。然而,在那些免疫疗法未充分增强LPR的患者(3/8)中,吲哚美辛改善了他们的淋巴细胞反应。在仅接受手术治疗的对照患者组中,吲哚美辛在术后六个月显著增强了体外LPR。尽管样本量较小,但我们的结果表明,T-激活素治疗对淋巴细胞增殖反应的增强作用可能至少部分归因于对前列腺素E介导的抑制细胞活性的影响。
此外,治疗后体外检测可能表明这种药物组合在一些早期黑色素瘤患者中具有潜在用途。