Ueyama S, Kawauchi H, Mogi G
Department of Otolaryngology, Medical College of Oita, Japan.
Arch Otolaryngol Head Neck Surg. 1988 Aug;114(8):878-82. doi: 10.1001/archotol.1988.01860200062019.
Effects of mucosa-derived T-suppressor cells on induction of IgG-mediated otitis media with effusion (OME) were investigated in mice, since antigen-antibody reactions in the tympanic cavity are pathogenic mechanisms of OME. Splenic T-suppressor cells from strain C3H/HeN female mice, to which ovalbumin (OVA) had been orally administered, were transferred intravenously to syngeneic mice. The mice receiving the T-suppressor cells were immunized with OVA intraperitoneally and then injected with OVA into the tympanic cavity. Nine of ten control mice, to which splenic T cells from saline-fed mice were administered, developed OME, while OME was seen in only one of ten mice receiving splenic T cells from OVA-fed mice. The results show that IgG-mediated OME can be suppressed to a certain extent by the induction of antigen-specific, mucosa-derived, T-suppressor cells.
由于鼓室内的抗原抗体反应是分泌性中耳炎(OME)的致病机制,因此研究了黏膜来源的T抑制细胞对IgG介导的分泌性中耳炎诱导的影响。将口服卵清蛋白(OVA)的C3H/HeN雌性小鼠的脾T抑制细胞静脉注射到同基因小鼠体内。接受T抑制细胞的小鼠经腹腔注射OVA免疫,然后向鼓室内注射OVA。给予来自生理盐水喂养小鼠的脾T细胞的十只对照小鼠中有九只发生了OME,而接受来自OVA喂养小鼠的脾T细胞的十只小鼠中只有一只出现了OME。结果表明,抗原特异性、黏膜来源的T抑制细胞的诱导可在一定程度上抑制IgG介导的OME。