TY - JOUR T1 - Keratinocyte growth factor and coeliac disease JF - Gut JO - Gut SP - 176 LP - 181 DO - 10.1136/gut.49.2.176 VL - 49 IS - 2 AU - V M Salvati AU - M Bajaj-Elliott AU - R Poulsom AU - G Mazzarella AU - K E A Lundin AU - E M Nilsen AU - R Troncone AU - T T MacDonald Y1 - 2001/08/01 UR - http://gut.bmj.com/content/49/2/176.abstract N2 - BACKGROUND Coeliac disease is characterised by increased epithelial renewal associated with a mucosal T cell response to gliadin. Keratinocyte growth factor (KGF) is produced by cytokine activated gut stromal cells and may be a link between mucosal T cell activation in untreated coeliac disease and epithelial hyperplasia.AIMS To characterise expression of KGF in coeliac disease.METHODS KGF transcripts in coeliac disease were measured by quantitative competitive reverse transcription-polymerase chain reaction (RT-PCR) and localised using in situ hybridisation. KGF production by gluten reactive CD4+ T cell clones was examined. In addition, KGF transcripts were measured following ex vivo challenge of coeliac biopsies with a peptic-tryptic digest of gliadin.RESULTS KGF transcripts were elevated in coeliac biopsies compared with normal controls but were not different from non-coeliac disease controls. By in situ hybridisation, KGF mRNA containing cells were present in the upper half of the lamina propria, most abundantly just under the epithelium. There was no signal from cells within the epithelium. Gluten reactive T cell clones did not make KGF. In vitro challenge of coeliac biopsies generated a strong interferon γ response but a specific KGF response could not be detected because of an extremely high number of KGF transcripts in all cultured biopsies.CONCLUSIONS KGF is overexpressed in coeliac biopsies and in tissues with non-coeliac enteropathy. No evidence was found for KGF production by intraepithelial lymphocytes or lamina propria T cells.CDcoeliac diseaseKGF (FGF-7)keratinocyte growth factorIELintraepithelial lymphocytesNCEnon-coeliac enteropathyRT-PCRreverse transcription-polymerase chain reactionIFN-γinterferon γIBDinflammatory bowel diseaseLPLlamina propria T cells ER -