Flow cytometric determination of aberrant intra-epithelial lymphocytes predicts T-cell lymphoma development more accurately than T-cell clonality analysis in Refractory Celiac Disease

被引:102
作者
Verbeek, Wieke H. M. [1 ]
Goerres, Marije S. [2 ]
von Blomberg, B. Mary E. [3 ]
Oudejans, Joost J. [2 ]
Scholten, Petra E. T. [3 ]
Hadithi, Muhammed [1 ]
Al-Toma, Abdul [1 ]
Schreurs, Marco W. J. [3 ]
Mulder, Chris J. J. [1 ]
机构
[1] Vrije Univ Amsterdam, Med Ctr, Dept Gastroenterol, NL-1007 MB Amsterdam, Netherlands
[2] Rijnstate Hosp, Dept Gastroenterol, Arnhem, Netherlands
[3] Vrije Univ Amsterdam, Med Ctr, Dept Pathol, Amsterdam, Netherlands
关键词
refractory celiac disease; flow cytometry; aberrant T-lymphocytes; immunophenotyping; enteropathy associated T-cell lymphoma; TCR gamma gene rearrangement; intraepithelial lymphocyte; clonality;
D O I
10.1016/j.clim.2007.09.002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: Refractory celiac disease (RCD) patients with aberrant, often clonal, intraepithelial. T-cells are at high risk for development of enteropathy associated T-cell lymphoma (EATL). Early detection of those patients that actually develop EATL is of utmost importance for curative intervention. Aim: First, to establish an optimal cut-off value for the percentage of aberrant lymphocytes, previously determined based on clinical observations, via reference ranges for aberrant T-cells in the duodenal mucosa of celiac disease patient and control groups. Secondly, to compare aberrancy with intestinal T-cell clonality as a prognostic parameter for EATL development in RCD. Methods: Immunophenotyping using flow cytometry was performed on small intestinal biopsy-derived lymphocytes, obtained from distinct celiac disease (CD) patient and control groups (N=167 in total). T-cell clonality in duodenal biopsy specimens was assessed by PCR in RCD, ulcerative jejunitis and EATL patients (N=31 in total). Results: In 95% of non-refractory CD patients, the highest percentage aberrant T-cells was 20%. Using this cut-off value, EATL development was exclusively seen in RCD with more than 20% aberrant T-cells (median 52% aberrant T-cells, range 27-94%). When compared with T-cell. clonality analysis, >20% aberrancy showed a much higher negative predictive value and sensitivity (both 100%) for EATL development in RCD patients than T-cell clonality analysis (respectively 75% and 78%). Conclusions: Quantification of aberrant T-cells by flow cytometry is preferable to T-cell clonality analysis for identification of RCD patients at risk for EATL development. A cut-off value of 20% is of use in risk stratification, therapeutic options and subsequent follow-up of RCD patients. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:48 / 56
页数:9
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