Bundo J, Watanabe N, Yoshida K, Mogi G
Department of Otolaryngology, Oita Medical Univesity, Japan.
Ann Otol Rhinol Laryngol. 1996 Oct;105(10):795-803. doi: 10.1177/000348949610501007.
We investigated influences of adhesion factors on the migration of antigen-specific IgA-forming cells (ASAFCs) to the middle ear mucosa by means of an in vitro lymphocyte binding assay. Peyer's patch (PP) lymphocytes from guinea pigs with mucosal immunization, which are rich in ASAFCs, more frequently bound with the inflamed middle ear mucosa than those of PP and spleen cells from animals with systemic immunization, in which antigen-specific IgG-forming cells (ASGFCs) were induced (p > .001). The bindings were not affected by antigenic and nonantigenic stimuli to the middle ear mucosa for producing otitis media. On human middle ear mucosa from 10 patients with acute mastoiditis and chronic otitis media, endothelial cells of newly grown vessels were stained strongly with intercellular adhesion molecule (ICAM)-1, and weakly with vascular cell adhesion molecule (VCAM)-1, platelet endothelial cell adhesion molecule (PECAM), and endothelial leukocyte adhesion molecule (ELAM)-1. Many lymphocytes bound mainly to these endothelial cells, and a few cells were observed bound to the basal portion of epithelial cells. The binding of lymphocytes was significantly, but not completely, inhibited by anti-ICAM-1 antibody (p < .001). These findings suggest that PP lymphocytes with activated mucosal immunity more frequently migrate to the inflamed middle ear mucosa, and that those migrations, after extravasation, may be regulated by the interaction between various binding factors and their receptors on lymphocytes, which is different from that of adhesion molecules and their ligands in the extravasation.
我们通过体外淋巴细胞结合试验,研究了黏附因子对中耳黏膜抗原特异性IgA形成细胞(ASAFCs)迁移的影响。经黏膜免疫的豚鼠派尔集合淋巴结(PP)淋巴细胞富含ASAFCs,与全身免疫动物的PP和脾细胞相比,其与炎症中耳黏膜的结合更为频繁,全身免疫动物诱导产生了抗原特异性IgG形成细胞(ASGFCs)(p>.001)。中耳黏膜受到抗原性和非抗原性刺激引发中耳炎时,这种结合不受影响。在10例急性乳突炎和慢性中耳炎患者的人中耳黏膜上,新生血管的内皮细胞被细胞间黏附分子(ICAM)-1强烈染色,而被血管细胞黏附分子(VCAM)-1、血小板内皮细胞黏附分子(PECAM)和内皮白细胞黏附分子(ELAM)-1弱染色。许多淋巴细胞主要与这些内皮细胞结合,少数细胞与上皮细胞基部结合。抗ICAM-1抗体可显著但不完全抑制淋巴细胞的结合(p<.001)。这些发现表明,具有活化黏膜免疫的PP淋巴细胞更频繁地迁移至炎症中耳黏膜,且这些迁移在渗出后可能受淋巴细胞上各种结合因子与其受体之间相互作用的调节,这与渗出过程中黏附分子及其配体的相互作用不同。