Department of Oral Pathology and Oral Medicine, School of Dental Medicine, Tel Aviv University, Tel Aviv, Israel.
Clin Oral Investig. 2013 Jun;17(5):1365-73. doi: 10.1007/s00784-012-0814-1. Epub 2012 Aug 15.
We sought to investigate the expression of cells with immunosuppressive/protumorigenic phenotypes in oral lichen planus (OLP), such as M2-tumor-associated macrophages (TAM2), myeloid-derived suppressive cells (MDSCs), and regulatory T cells (Tregs) in association with clinical parameters.
Cases of hyperkeratotic (HK)-OLP (n = 23) and erosive (E)-OLP (n = 26) were immunohistochemically stained to determine the percentages of CD163-TAM2, CD80-MDSCs, and FOXP3-Tregs of proinflammatory CD121a-Th17, CD4 and CD8 lymphocytes, and of cells positive for nuclear factor kappa B (NF-κB) and transforming growth factor beta. Clinical parameters included symptoms, treatment approach, treatment response, and others.
The inflammatory infiltrate in HK-OLP and E-OLP contained immunosuppressive cells; however, their pattern of expression was compatible with a proinflammatory response [membranous CD163-TAM2 staining (not extracellular), CD80+ lymphocytes (not macrophages), and a few Tregs]. The presence of CD4+, CD8+, and CD121a+ T lymphocytes was extensive. TAM2 were more frequent in E-OLP than in HK-OLP (P = 0.017). A higher frequency of CD80+ lymphocytes was associated with partial to no response to treatment (P = 0.028). Nuclear expression of NF-κB in the inflammatory cells was absent.
The pattern of expression of the immunosuppressive cells, together with numerous CD4+, CD8+, and Th17-CD121a+ lymphocytes, suggest an extensive proinflammatory response rather than an immunosuppressive/protumorigenic response.
The frequency of selective types of inflammatory cells calls for individual profile analyses of inflammatory infiltrates and individually adjusted treatment.
我们旨在研究口腔扁平苔藓(OLP)中具有免疫抑制/促肿瘤表型的细胞的表达,例如 M2-肿瘤相关巨噬细胞(TAM2)、髓系来源的抑制细胞(MDSCs)和调节性 T 细胞(Tregs),并将其与临床参数相关联。
对 23 例角化过度(HK)-OLP 和 26 例糜烂(E)-OLP 病例进行免疫组织化学染色,以确定促炎 CD121a-Th17、CD4 和 CD8 淋巴细胞以及核因子 kappa B(NF-κB)和转化生长因子β阳性细胞的 CD163-TAM2、CD80-MDSCs 和 FOXP3-Tregs 的比例。临床参数包括症状、治疗方法、治疗反应等。
HK-OLP 和 E-OLP 中的炎症浸润含有免疫抑制细胞;然而,它们的表达模式与促炎反应一致[膜性 CD163-TAM2 染色(非细胞外)、CD80+淋巴细胞(非巨噬细胞)和少数 Tregs]。CD4+、CD8+和 CD121a+T 淋巴细胞广泛存在。E-OLP 中的 TAM2 比 HK-OLP 更为常见(P=0.017)。CD80+淋巴细胞的频率较高与部分或无治疗反应相关(P=0.028)。炎症细胞中的 NF-κB 核表达缺失。
免疫抑制细胞的表达模式以及大量的 CD4+、CD8+和 Th17-CD121a+淋巴细胞提示广泛的促炎反应,而不是免疫抑制/促肿瘤反应。
选择性炎症细胞的频率需要对炎症浸润物进行单独的分析,并进行个体化的治疗调整。