Pforte A, Breyer G, Prinz J C, Gais P, Burger G, Häussinger K, Rieber E P, Held E, Ziegler-Heitbrock H W
Medical Department Innenstadt, University of Munich, Federal Republic of Germany.
J Exp Med. 1990 Apr 1;171(4):1163-9. doi: 10.1084/jem.171.4.1163.
Expression of the Fc receptor for IgE (Fc epsilon R) was analyzed on alveolar macrophages (AM) in 10 patients with extrinsic allergic alveolitis (EAA) compared with 10 patients with sarcoidosis and to 6 apparently healthy controls. By using the anti-Fc epsilon RII mAb M-L25 in immunocytochemistry experiments, we found that greater than 60% of AM in 10 of 10 patients with EAA were strongly positive, as evidenced by visual analysis in light microscopy and by cytometry. By contrast, no significant staining was detected in sarcoidosis or in controls with either method. Similar results were obtained when Fc epsilon R were identified with preformed immune complexes consisting of NIP-specific human/mouse chimeric IgE antibody plus NIP-ovalbumin. Furthermore, greater than 60% of AM in patients with EAA stained positive for IgE, demonstrating that endogenous IgE is bound to the AM. Our data suggest that IgE antibodies bound to Fc epsilon RII on AM may be involved in pathophysiology of extrinsic allergic alveolitis by activation of the AM after binding of allergen to the cell surface IgE. Furthermore, with the clearcut pattern of Fc epsilon RII expression in extrinsic allergic alveolitis it may be possible to use CD23 antibodies for differential diagnosis of inflammatory lung disease.
对10例过敏性肺炎(EAA)患者、10例结节病患者及6例健康对照者的肺泡巨噬细胞(AM)上的IgE Fc受体(FcεR)表达进行了分析。在免疫细胞化学实验中使用抗FcεRII单克隆抗体M-L25,我们发现,在10例EAA患者中,10例患者中有超过60%的AM呈强阳性,光学显微镜下的视觉分析和细胞计数法均证实了这一点。相比之下,在结节病患者或对照组中,两种方法均未检测到明显的染色。当用由NIP特异性人/鼠嵌合IgE抗体加NIP-卵清蛋白组成的预形成免疫复合物鉴定FcεR时,也获得了类似的结果。此外,EAA患者中超过60%的AM对IgE染色呈阳性,表明内源性IgE与AM结合。我们的数据表明,AM上与FcεRII结合的IgE抗体可能通过变应原与细胞表面IgE结合后激活AM而参与过敏性肺炎的病理生理过程。此外,鉴于过敏性肺炎中FcεRII表达模式明确,有可能使用CD23抗体对炎症性肺病进行鉴别诊断。