Author/Authors :
Enarsson، نويسنده , , K. and Johnsson، نويسنده , , E. and Lindholm، نويسنده , , C. and Lundgren، نويسنده , , A. and Pan-Hammarstrِm، نويسنده , , Q. and Strِmberg، نويسنده , , E. and Bergin، نويسنده , , P. and Baunge، نويسنده , , E.-L. and Svennerholm، نويسنده , , A.-M. and Quiding-Jنrbrink، نويسنده , , M.، نويسنده ,
Abstract :
Worldwide, gastric adenocarcinoma (GC) is the second most common cause of death from malignant disease. The reason why immune responses are unable to clear the tumour is not fully understood, although aberrant lymphocyte recruitment to the tumour site might be one factor. Therefore, we investigated the homing phenotype of mucosal T lymphocytes in GC, compared to tumour-free mucosa.
ld detect significantly decreased frequencies of mucosal homing α4β7+ T cells in the tumour tissues and increased frequencies of L-selectin+ T cells. This was probably due to the correlated decrease in MAdCAM-1 positive and increase in PNAd positive blood vessels in the tumour mucosa. There were also fewer CXCR3+ T lymphocytes in the tumour tissue. These findings provide evidence that endothelial cells within tumours arising at mucosal sites do not support extravasation of typical mucosa-infiltrating T cells. This may be of major relevance for future immunotherapeutic strategies for treatment of GC.
Keywords :
gastric adenocarcinoma , Helicobacter pylori , human , Cell recruitment , Endothelial addressins , cell adhesion molecules