Nakano Y, Nakano K
Immunology. 1985 Feb;54(2):297-305.
The mechanisms of non-specific unresponsiveness to contact sensitivity (CS) induced with intravenous (i.v.) administration of oxazolone (Ox)-conjugated syngeneic spleen cells was investigated. Non-specific suppressor cells were found in spleen cells of mice which had been injected i.v. with Ox-conjugated cells 7 days before. These non-specific suppressor cells blocked the efferent stage of CS profoundly, i.e. inhibited the activity of effector cells for picryl chloride (PCl). Since these suppressor cells were plastic-adherent and resistant to treatment with anti-Thy 1.2 antibody and complement, they were considered to be macrophage-like. These suppressor cells released non-specific suppressor factor(s) (NSF) during culture for 1 hr without any antigenic triggering. Effector cells for PCl which were treated with NSF for 1 hr at 4 degrees lost their ability to transfer CS. NSF was easily absorbed by normal spleen cells. Furthermore, these NSF-treated spleen cells acquired the ability to inhibit the passive transfer of CS non-specifically. We also discussed the pathway for the induction of these macrophage-like suppressor cells.
研究了静脉注射恶唑酮(Ox)偶联的同基因脾细胞诱导的对接触敏感性(CS)的非特异性无反应机制。在7天前静脉注射Ox偶联细胞的小鼠脾细胞中发现了非特异性抑制细胞。这些非特异性抑制细胞深刻地阻断了CS的传出阶段,即抑制了对苦味酸氯(PCl)的效应细胞的活性。由于这些抑制细胞具有贴壁性且对抗-Thy 1.2抗体和补体处理有抗性,它们被认为是巨噬细胞样的。这些抑制细胞在无任何抗原触发的情况下培养1小时期间释放非特异性抑制因子(NSF)。在4℃下用NSF处理1小时的PCl效应细胞失去了传递CS的能力。NSF很容易被正常脾细胞吸收。此外,这些经NSF处理的脾细胞获得了非特异性抑制CS被动转移的能力。我们还讨论了这些巨噬细胞样抑制细胞的诱导途径。