Department of Immunohematology, Leiden University Medical Center, Albinusdreef 2, 2333 ZA Leiden, The Netherlands.
Gut. 2013 Apr;62(4):509-19. doi: 10.1136/gutjnl-2012-302265. Epub 2012 Jul 3.
Refractory coeliac disease type II (RCDII) is a severe complication of coeliac disease (CD) characterised by aberrant intraepithelial lymphocytes (IELs) of unknown origin that display an atypical CD3(-)CD7(+)icCD3(+) phenotype. In approximately 40% of patients with RCDII these lymphocytes develop into an invasive lymphoma. In the current study we aimed to identify the physiological counterpart of these cells.
RCDII cell lines were compared with T-cell receptor positive (TCR(+)) IEL (T-IEL) lines by microarray analysis, real-time quantitative PCR and flow cytometry. This information was used to identify cells with an RCDII-associated phenotype in duodenal biopsies from non-refractory individuals by multicolour flow cytometry.
RCDII lines were transcriptionally distinct from T-IEL lines and expressed higher levels of multiple natural killer (NK) cell receptors. In addition to the CD3(-)CD7(+)icCD3(+) phenotype, the RCDII lines were distinguishable from other lymphocyte subsets by the absence of CD56, CD127 and CD34. Cells matching this surface lineage-negative (Lin(-)) CD7(+)CD127(-)CD34(-) phenotype expressed a functional interleukin-15 (IL-15) receptor and constituted a significant proportion of IELs in duodenal specimens of patients without CD, particularly children, and were also found in the thymus. In patients without CD, the Lin(-)CD7(+)CD127(-)CD34(-) subset was one of four subsets within the CD3(-)CD7(+)icCD3(+) population that could be distinguished on the basis of differential expression of CD56 and/or CD127.
Our studies indicate that the CD3(-)CD7(+)icCD3(+) population is heterogeneous and reveal the existence of a Lin(-) subset that is distinct from T, B, NK and lymphoid tissue inducer cells. We speculate that this IL-15 responsive population represents the physiological counterpart of aberrant cells expanded in RCDII and transformed in RCDII-associated lymphoma.
难治性乳糜泻 II 型(RCDII)是乳糜泻(CD)的一种严重并发症,其特征为来源不明的异常上皮内淋巴细胞(IEL),这些细胞表现出非典型的 CD3(-)CD7(+)icCD3(+)表型。在大约 40%的 RCDII 患者中,这些淋巴细胞会发展为侵袭性淋巴瘤。在目前的研究中,我们旨在确定这些细胞的生理对应物。
通过微阵列分析、实时定量 PCR 和流式细胞术比较 RCDII 细胞系与 T 细胞受体阳性(TCR(+))IEL(T-IEL)系。利用这些信息,通过多色流式细胞术鉴定非难治性个体十二指肠活检中具有 RCDII 相关表型的细胞。
RCDII 系与 T-IEL 系在转录水平上存在差异,并且表达更高水平的多种自然杀伤(NK)细胞受体。除了 CD3(-)CD7(+)icCD3(+)表型外,RCDII 系还可以通过缺乏 CD56、CD127 和 CD34 与其他淋巴细胞亚群区分开来。与这种表面谱系阴性(Lin(-))CD7(+)CD127(-)CD34(-)表型匹配的细胞表达功能性白细胞介素 15(IL-15)受体,并且构成 CD 患者十二指肠标本中 IEL 的重要组成部分,尤其是儿童,并且也存在于胸腺中。在无 CD 的患者中,Lin(-)CD7(+)CD127(-)CD34(-)亚群是 CD3(-)CD7(+)icCD3(+)群体中可以基于 CD56 和/或 CD127 的差异表达来区分的四个亚群之一。
我们的研究表明,CD3(-)CD7(+)icCD3(+)群体是异质的,并揭示了存在一个 Lin(-)亚群,该亚群与 T、B、NK 和淋巴组织诱导细胞不同。我们推测,这个 IL-15 反应性群体代表了 RCDII 中扩增和转化为 RCDII 相关淋巴瘤的异常细胞的生理对应物。