Cuida M, Brun J G, Johannessen A C, Jonsson R
Broegelmann Research Laboratory for Microbiology, University of Bergen, Norway.
APMIS. 1996 Dec;104(12):881-90. doi: 10.1111/j.1699-0463.1996.tb04953.x.
The aim of this study was to analyse the nature of infiltrating cells in minor salivary glands of patients with Sjögren's syndrome (SS). Furthermore, we wanted to characterize the tissue distribution of calprotectin-producing cells in inflamed salivary gland tissue of SS and in synovial tissue of patients with rheumatoid arthritis (RA) and osteoarthritis (OA). Cryostat sections of labial salivary gland tissue from patients with SS and synovial tissue from RA and OA patients were stained (ABC-immunoperoxidase technique) using monoclonal antibodies (MoAbs) to T cells (CD3), monocytes/macrophages (CD14, CD68), and calprotectin. Monocytes and macrophages were widely distributed in focal infiltrates of salivary gland tissue from SS patients. Calprotectin markers showed a distinct staining of infiltrating macrophages and around blood vessel walls. In synovial tissue samples, calprotectin was expressed in a high percentage of cells in the synovial lining, the subsynovium, and vessel walls. The percentages of cells stained for calprotectin were significantly higher in RA than in OA and SS tissues. Antibodies to the calprotectin complex stained cells with a similar distribution as antibodies against the separate polypeptide chains of calprotectin. The localization and differentiated expression of calprotectin in these chronic inflammatory conditions indicate a role in the inflammatory process and may be an additional marker of macrophages/granulocytes in SS, RA and OA.
本研究的目的是分析干燥综合征(SS)患者小唾液腺中浸润细胞的性质。此外,我们还想明确SS炎症唾液腺组织以及类风湿关节炎(RA)和骨关节炎(OA)患者滑膜组织中产生钙卫蛋白的细胞的组织分布情况。使用针对T细胞(CD3)、单核细胞/巨噬细胞(CD14、CD68)和钙卫蛋白的单克隆抗体(MoAbs),对SS患者的唇唾液腺组织冰冻切片以及RA和OA患者的滑膜组织进行染色(ABC免疫过氧化物酶技术)。单核细胞和巨噬细胞广泛分布于SS患者唾液腺组织的局灶性浸润中。钙卫蛋白标记物显示浸润的巨噬细胞和血管壁周围有明显染色。在滑膜组织样本中,钙卫蛋白在滑膜衬里、滑膜下层和血管壁的高比例细胞中表达。RA组织中钙卫蛋白染色细胞的百分比显著高于OA和SS组织。针对钙卫蛋白复合物的抗体与针对钙卫蛋白单独多肽链的抗体染色细胞的分布相似。钙卫蛋白在这些慢性炎症状态下的定位和差异表达表明其在炎症过程中发挥作用,可能是SS、RA和OA中巨噬细胞/粒细胞的另一种标志物。