© 2002 by Gut
COMMENTARY
Gut immunology
From hyperplasia to T cell lymphoma
1 INSERM EPI-9925, Faculté Necker-Enfants Malades, Paris, France
2 INSERM EPI-9925, Faculté Necker-Enfants Malades, and Department of Pathology, Hôpital Necker-Enfants Malades, Paris, France
3 INSERM EPI-9925, Faculté Necker-Enfants Malades, and Department of Gastroenterology, Hôpital Européen Georges Pompidou, Paris, France
Correspondence to:
Correspondence to:
N Cerf-Bensussan, INSERM EPI-9925, Faculté Necker-Enfants Malades, 156 Rue de Vaugirard, 75737 Paris Cedex 15, France;
cerf@necker.fr.
Disturbances in intraepithelial lymphocyte homeostasis in coeliac disease may lead to the emergence of lymphoid malignancies
Keywords: refractory sprue; immunohistochemistry; intraepithelial lymphocytes; CD30; T cell lymphoma; enteropathy
| The first 150 words of the full text of this article appear below. |
Enteropathy-type intestinal T cell lymphomas (EITCL) are a recognised complication of coeliac disease (CD).1 A recent survey confirmed that non-Hodgkin lymphomas, although rare, are the main cause of mortality in CD.2 The mechanisms favouring the development of EITCL in CD patients but not in other chronic inflammatory bowel diseases remain elusive, but mounting evidence points to a profound disturbance in intraepithelial lymphocyte (IEL) homeostasis, leading to the emergence of lymphoid malignancies. A link between IELs and EITCL was first advocated in 1988 by Spencer et al who observed that most EITCL expressed the CD103 IEL marker.3 Two complementary observations suggested that EITCL derive from a reactive T cell population present in the intestine of CD patients: thus the same T cell clonal rearrangement was detected by Murray et al in EITCL and in the adjacent non-tumoral flat mucosa,4 and by Ashton-Key et al in non-lymphomatous ulcers of ulcerative
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