Facchetti F, Signorini S, Majorana A, Manganoni M A, Sapelli P, Imberti L
Department of Pathology, University of Brescia, Spedali Civili Brescia, Italy.
J Oral Pathol Med. 2000 Nov;29(10):519-22. doi: 10.1034/j.1600-0714.2000.291007.x.
Orofacial granulomatosis (OFG) represents an inflammatory disorder of the facial and oral mucosa, histologically characterized by non-caseating epithelioid cell granulomas. Since other granulomatous diseases have been shown to be characterized by a limited heterogeneity of alpha/beta and gamma/delta T cells, we investigated the T-cell diversity of both types of lymphocytes obtained from the same OFG patient. When we compared the T-cell receptor diversity of the lymphocytes accumulating at the site of the lesions with that of the peripheral blood counterpart, we did not find significant differences. Furthermore, no exclusive expansions of different T-cell clones were seen in the patient. From these data we conclude that, in this OFG patient, the majority of T cells have no specificity for a single or for a few antigens and that tissue accumulation of T lymphocytes is the result of a random influx of cells at the site of inflammation.
口面部肉芽肿病(OFG)是一种面部和口腔黏膜的炎症性疾病,组织学特征为非干酪样上皮样细胞肉芽肿。由于其他肉芽肿性疾病已被证明具有α/β和γ/δ T细胞有限的异质性,我们研究了从同一名OFG患者获得的这两种淋巴细胞的T细胞多样性。当我们比较病变部位积聚的淋巴细胞与外周血对应淋巴细胞的T细胞受体多样性时,未发现显著差异。此外,在该患者中未观察到不同T细胞克隆的特异性扩增。根据这些数据我们得出结论,在这名OFG患者中,大多数T细胞对单一或少数抗原无特异性,并且T淋巴细胞的组织积聚是炎症部位细胞随机流入的结果。