Yamamoto T, Yoneda K, Ueta E, Osaki T
Department of Oral Surgery, Kochi Medical School, Japan.
J Oral Pathol Med. 1990 Nov;19(10):464-70. doi: 10.1111/j.1600-0714.1990.tb00788.x.
Functions of peripheral blood lymphocytes and neutrophils from 30 oral lichen planus (OLP) patients were examined using healthy persons as controls. Two-color flow cytometry of lymphocytes revealed no proportional difference in CD3 or CD4 cells between OLP and controls. CD8CD11b (suppressor T) and CD3HLA-DR+ cell populations increased significantly in OLP when compared with controls, and CD4/CD8 cell ratio decreased in OLP. Mitogenic response of patients' CD8 and CD4Leu8- cells was similar to that in controls. However, weaker blastogenesis of CD4Leu8+ cells, the most excellent responders in T cell subsets, was observed in OLP. Serum IFN beta level in OLP (8.4 +/- 4.8 IU/ml) was significantly lower than in controls (13.7 +/- 5.0 IU/ml) whereas no difference between the two groups could be found in IFN alpha or gamma. As for in vitro cytokine production by IL-2-stimulated lymphocytes, there was no difference in GM-CSF generation between the two groups, but, IFN gamma and IL1 beta production of patients' lymphocytes was less than that in healthy donors (57.6 +/- 50.7 VS 78.7 +/- 39.6 u/ml, 152.3 +/- 93.5 VS 258.7 +/- 65.4 pg/ml, respectively). Moreover, superoxide generation of patients' neutrophils by PMA stimulation was significantly insufficient as compared with controls' (84.9 +/- 30.9 VS 110.8 +/- 24.1 pmol/min/10(4) cells). Nevertheless, natural killer cell activities of both groups distributed in the same range. These results suggest that OLP patients' lymphocyte and neutrophil functions are impaired, and that cellular immunosuppression is a pathologic characteristic of OLP.
以健康人为对照,检测了30例口腔扁平苔藓(OLP)患者外周血淋巴细胞和中性粒细胞的功能。淋巴细胞双色流式细胞术显示,OLP患者与对照组之间CD3或CD4细胞比例无差异。与对照组相比,OLP患者的CD8CD11b(抑制性T细胞)和CD3HLA-DR+细胞群体显著增加,且OLP患者的CD4/CD8细胞比值降低。患者CD8和CD4Leu8-细胞的促有丝分裂反应与对照组相似。然而,在OLP患者中观察到,T细胞亚群中反应最强烈的CD4Leu8+细胞的增殖能力较弱。OLP患者血清IFN-β水平(8.4±4.8 IU/ml)显著低于对照组(13.7±5.0 IU/ml),而两组在IFN-α或γ水平上无差异。至于IL-2刺激的淋巴细胞体外细胞因子产生情况,两组之间GM-CSF的产生无差异,但患者淋巴细胞的IFN-γ和IL-1β产生低于健康供体(分别为57.6±50.7与78.7±39.6 u/ml,152.3±93.5与258.7±65.4 pg/ml)。此外,与对照组相比,患者中性粒细胞经佛波酯(PMA)刺激产生的超氧化物显著不足(84.9±30.9与110.8±24.1 pmol/min/10(4)细胞)。然而,两组的自然杀伤细胞活性分布在相同范围内。这些结果表明,OLP患者的淋巴细胞和中性粒细胞功能受损,细胞免疫抑制是OLP的病理特征。