McMenamin C, Girn B, Holt P G
Division of Cell Biology, Western Australia Research Institute for Child Health, Princess Margaret Hospital, Subiaco.
Immunology. 1992 Dec;77(4):592-6.
Repeated exposure of high-IgE responder rats to antigen-containing aerosols stimulates IgE responses which last for several weeks, and are eventually terminated with the onset of immunological tolerance. Studies on the distribution of total and antigen-specific IgE plasma cells and IgE mRNA during antibody production, identified the lymph nodes draining the lower respiratory tract as the primary site for initiation of the IgE response to inhaled antigen; subsequently the response seeded to mucosa-associated lymph nodes but not to central lymphoid organs. A vigorous 'bystander' IgE response (approx. x 10 the specific response) was also observed, but this was restricted to areas directly draining sites of deposition of inhaled antigen, including non-lymphoid respiratory mucosal tissues. Despite the rapid termination of the specific IgE response after the fourth week of exposure, the bystander component persisted. These results are discussed in relation to the role of cognate/non-cognate T-B interactions in the IgE response to inhaled antigens, and the relative susceptibility of each component to T-cell regulation in vivo.
高IgE反应大鼠反复暴露于含抗原的气溶胶中会刺激IgE反应,该反应持续数周,并最终随着免疫耐受的出现而终止。在抗体产生过程中对总IgE和抗原特异性IgE浆细胞以及IgE mRNA分布的研究表明,引流下呼吸道的淋巴结是对吸入抗原产生IgE反应的起始主要部位;随后该反应扩散至黏膜相关淋巴结,但未扩散至中枢淋巴器官。还观察到强烈的“旁观者”IgE反应(约为特异性反应的10倍),但这仅限于直接引流吸入抗原沉积部位的区域,包括非淋巴性呼吸黏膜组织。尽管在暴露第四周后特异性IgE反应迅速终止,但旁观者成分仍持续存在。本文结合同源/非同源T-B相互作用在对吸入抗原的IgE反应中的作用,以及各成分在体内对T细胞调节的相对敏感性,对这些结果进行了讨论。