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活动性乳糜泻与难治性乳糜泻中小肠白细胞产生的差异白介素 13。

Differential IL-13 production by small intestinal leukocytes in active coeliac disease versus refractory coeliac disease.

机构信息

Department of Pathology, VU University Medical Center, Amsterdam, The Netherlands.

出版信息

Mediators Inflamm. 2013;2013:939047. doi: 10.1155/2013/939047. Epub 2013 Apr 15.

DOI:10.1155/2013/939047
PMID:23690672
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3649694/
Abstract

A small fraction of coeliac disease (CD) patients have persistent villous atrophy despite strict adherence to a gluten-free diet. Some of these refractory CD (RCD) patients develop a clonal expansion of lymphocytes with an aberrant phenotype, referred to as RCD type II (RCDII). Pathogenesis of active CD (ACD) has been shown to be related to gluten-specific immunity whereas the disease is no longer gluten driven in RCD. We therefore hypothesized that the immune response is differentially regulated by cytokines in ACD versus RCDII and investigated mucosal cytokine release after polyclonal stimulation of isolated mucosal lymphocytes. Secretion of the T(H)2 cytokine IL-13 was significantly higher in lamina propria leukocytes (LPLs) isolated from RCDII patients as compared to LPL from ACD patients (P = 0.05). In patients successfully treated with a gluten-free diet LPL-derived IL-13 production was also higher as compared to ACD patients (P = 0.02). IL-13 secretion correlated with other T(H)2 as well as T(H)1 cytokines but not with IL-10 secretion. Overall, the cytokine production pattern of LPL in RCDII showed more similarities with LPL isolated from GFD patients than from ACD patients. Our data suggest that different immunological processes are involved in RCDII and ACD with a potential role for IL-13.

摘要

一小部分乳糜泻 (CD) 患者尽管严格遵循无麸质饮食,但仍存在持续的绒毛萎缩。这些难治性 CD (RCD) 患者中的一些会出现淋巴细胞克隆性扩张,表现为异常表型,称为 RCD II 型 (RCDII)。已表明活动性 CD (ACD) 的发病机制与麸质特异性免疫有关,而在 RCD 中,疾病不再由麸质驱动。因此,我们假设免疫反应在 ACD 与 RCDII 之间受到细胞因子的不同调节,并研究了分离的黏膜淋巴细胞多克隆刺激后黏膜细胞因子的释放。与 ACD 患者相比,RCDII 患者的固有层白细胞 (LPL) 中 T(H)2 细胞因子 IL-13 的分泌显著更高 (P = 0.05)。在接受无麸质饮食成功治疗的患者中,LPL 衍生的 IL-13 产生也高于 ACD 患者 (P = 0.02)。IL-13 分泌与其他 T(H)2 和 T(H)1 细胞因子相关,但与 IL-10 分泌无关。总体而言,RCDII 中 LPL 的细胞因子产生模式与从 GFD 患者中分离的 LPL 更相似,而与 ACD 患者中分离的 LPL 更相似。我们的数据表明,RCDII 和 ACD 涉及不同的免疫过程,IL-13 可能具有潜在作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a11/3649694/feb83ba5aaef/MI2013-939047.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a11/3649694/934f8dd100ce/MI2013-939047.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a11/3649694/bb7c33da0383/MI2013-939047.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a11/3649694/feb83ba5aaef/MI2013-939047.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a11/3649694/934f8dd100ce/MI2013-939047.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a11/3649694/bb7c33da0383/MI2013-939047.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a11/3649694/feb83ba5aaef/MI2013-939047.003.jpg

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