Mannhalter J W, Zlabinger G J, Ahmad R, Eibl M M
Clin Exp Immunol. 1983 Oct;54(1):95-102.
Interactions of human T cells and macrophages/monocytes (MOs) following stimulation by a Gram negative micro-organism (E. coli) have been investigated. Immunoadsorption studies showed that the E. coli-induced proliferative response of human T cells was antigen specific. The T cell pool could be selectively depleted of E. coli reactive cells by short exposure to autologous E. coli pulsed Møs. This treatment did not remove T cell reactivity directed towards an unrelated antigen (tetanus toxoid). This demonstrated the antigen specificity of the immunoadsorption step, which was further confirmed by reconstitution of E. coli reactivity after supplementing the adsorbed T cell pool with E. coli specific T cells. The Mø requirement for the E. coli-induced T cell response was confirmed and kinetic studies showed a dose-dependence with respect to the amount of E. coli used for both E. coli-induced T cell proliferation and the efficiency of immunoadsorption.
对革兰氏阴性微生物(大肠杆菌)刺激后人T细胞与巨噬细胞/单核细胞(MOs)之间的相互作用进行了研究。免疫吸附研究表明,大肠杆菌诱导的人T细胞增殖反应具有抗原特异性。通过短时间暴露于自体大肠杆菌脉冲处理的巨噬细胞,可选择性地耗尽T细胞库中对大肠杆菌有反应的细胞。这种处理并未消除针对无关抗原(破伤风类毒素)的T细胞反应性。这证明了免疫吸附步骤的抗原特异性,在用大肠杆菌特异性T细胞补充吸附后的T细胞库后,大肠杆菌反应性的重建进一步证实了这一点。对大肠杆菌诱导的T细胞反应中巨噬细胞的需求得到了证实,动力学研究表明,对于用于大肠杆菌诱导的T细胞增殖和免疫吸附效率的大肠杆菌量,存在剂量依赖性。