Tonn T, Esser C, Schneider E M, Steinmann-Steiner-Haldenstätt W, Gleichmann E
Medical Institute of Environmental Hygiene, University of Düsseldorf, Germany.
Environ Health Perspect. 1996 Apr;104(4):422-6. doi: 10.1289/ehp.96104422.
In experimentally exposed animals 2,3,7,8-tetrachlorodibenzo-n-dioxin (TCDD) causes severe immunosuppression. However, the overall susceptibility of humans for the different pathological effects of TCDD has remained unclear. We examined the long-term effects of TCDD in 11 industrial workers who were exposed to high doses of TCDD for several years 20 years ago. Current TCDD body burdens were still at least 10 times higher (between 43 and 874 pg/g blood far) in these exposed persons than in the average German population. To evaluate possible TCDD-induced changes in the percentage of different lymphocyte subsets, we determined a large panel of lymphocyte subsets in the blood by flow cytometric analysis. Immunocompetence of T-and B-lymphocytes was tested by nitrogen (phytohemagglutinin, pokeweed mitogen)- induced lymphoproliferation assays and by assays using sensitive mixed-lymphocyte cultures. No significant differences could be detected between the individuals tested and controls for surface marker distribution or mitogen-induced lymphoproliferation TCDD-exposed subjects showed a reduced response to human lymphocyte antigen-allogeneic lymphocytes and interleukin-2-boosted proliferation. Responder cells of the dioxin-exposed persons proliferated less in response to irradiated stimulator cells (p < or = 0.05), and the third-party mixed lymphocyte reaction against unirradiated stimulator cells revealed suppressive activity in the responder cell fraction compared to the controls (p < or = 0.01). Furthermore, the capacity of a pool of T cells isolated from TCDD-exposed subjects to proliferate upon interleukin-2 stimulation was significantly diminished (p < or = 0.05). TCDD has a long-term immunosuppressive-effect on T-helper cell function, which is mediated more likely by a reduced functionality of individual cells rather than by a reduction in absolute cell numbers in the peripheral blood.
在实验暴露的动物中,2,3,7,8-四氯二苯并对二恶英(TCDD)会导致严重的免疫抑制。然而,人类对TCDD不同病理效应的总体易感性仍不明确。我们研究了20年前曾接触高剂量TCDD数年的11名产业工人中TCDD的长期影响。这些接触者目前体内的TCDD负荷仍比德国普通人群至少高10倍(血液中TCDD含量在43至874皮克/克之间)。为评估TCDD可能引起的不同淋巴细胞亚群百分比变化,我们通过流式细胞术分析测定了血液中大量的淋巴细胞亚群。通过氮(植物血凝素、商陆有丝分裂原)诱导的淋巴细胞增殖试验以及使用敏感的混合淋巴细胞培养试验检测T细胞和B细胞的免疫活性。在检测的个体与对照组之间,未检测到表面标志物分布或有丝分裂原诱导的淋巴细胞增殖有显著差异。接触TCDD的受试者对人淋巴细胞抗原-异体淋巴细胞和白细胞介素-2增强的增殖反应降低。二恶英接触者的反应细胞对经辐照的刺激细胞增殖较少(p≤0.05),与对照组相比,针对未经辐照的刺激细胞进行的第三方混合淋巴细胞反应显示反应细胞部分具有抑制活性(p≤0.01)。此外,从接触TCDD的受试者中分离出的一组T细胞在白细胞介素-2刺激下增殖的能力显著降低(p≤0.05)。TCDD对辅助性T细胞功能具有长期免疫抑制作用,这种作用更可能是由单个细胞功能降低介导的,而非外周血中绝对细胞数量减少所致。