Hirszfeld Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, R. Weigla 12, 53-114, Wroclaw, Poland.
Lower Silesian Center for Cellular Transplantation and National Bone Marrow Donor Registry, Wroclaw, Poland.
Arch Immunol Ther Exp (Warsz). 2019 Oct;67(5):311-323. doi: 10.1007/s00005-019-00549-2. Epub 2019 Jun 8.
Excessive inflammatory environment in a course of chronic graft-versus-host disease (cGvHD) is associated with T-cell trafficking into inflamed tissues. This study focused on the identification of IL-17-producing cells in the tissue biopsies of cGvHD patients. Forty-one biopsy specimens of cGvHD lesions of the skin (n = 27), gastrointestinal tract (n = 9) and oral mucosa (n = 5), examined in 24 patients, were morphologically defined according to the NIH criteria and analyzed for the presence of cellular infiltrations including: IL-17, FOXP3 and CCR6 cells. IL-17 cells were identified in 26/27 skin and in all gut and oral mucosa biopsies, being more frequent in mucosa lesions than in the skin (11/14 vs 14/26, respectively; NS: not significant). Double staining documented that CD138/IL-17 cells were commonly seen in the gut than in the skin (5/8 vs 3/11, respectively; NS). In the skin, cells expressing trafficking receptor CCR6 were more frequent than IL-17 cells compared to the mucosa (23/26 vs 2/13, respectively; p < 0.0001). CCR6 was present on a majority of IL-17 cells in all examined skin biopsies but only in 6 out of 11 digestive tract biopsies (p = 0.0112). FOXP3 cells were identified only in five patients (with mild lesions) at least in one biopsy. In this study group, results documented that local expansion of IL-17-producing cells in the digestive tract correlate with moderate and severe clinical symptoms of cGvHD, in contrast to the skin, where IL-17 cells are rather scarcely present (p = 0.0301) and the course of cGvHD is slowly progressing with final organ deterioration.
慢性移植物抗宿主病(cGvHD)过程中过度的炎症环境与 T 细胞向炎症组织的迁移有关。本研究旨在鉴定 cGvHD 患者组织活检中的 IL-17 产生细胞。在 24 例患者中,对 41 例皮肤(n=27)、胃肠道(n=9)和口腔黏膜(n=5)cGvHD 病变的活检标本进行了形态学定义,根据 NIH 标准进行了分析,以确定细胞浸润的存在,包括:IL-17、FOXP3 和 CCR6 细胞。在 26/27 例皮肤和所有肠道和口腔黏膜活检中均发现了 IL-17 细胞,黏膜病变比皮肤更常见(11/14 比 14/26,分别;NS:无显著性差异)。双重染色表明,CD138/IL-17 细胞在肠道比在皮肤更常见(5/8 比 3/11,分别;NS)。在皮肤中,表达趋化因子受体 CCR6 的细胞比黏膜中更常见(23/26 比 2/13,分别;p<0.0001)。在所有检查的皮肤活检中,CCR6 存在于大多数 IL-17 细胞上,但仅在 11 例消化道活检中的 6 例中存在(p=0.0112)。FOXP3 细胞仅在至少 1 例活检中在 5 例患者(轻度病变)中被识别。在本研究组中,结果表明,消化道中 IL-17 产生细胞的局部扩增与 cGvHD 的中度和重度临床症状相关,与皮肤相反,皮肤中 IL-17 细胞很少存在(p=0.0301),cGvHD 的病程进展缓慢,最终导致器官恶化。