Differential mechanisms for T lymphocyte recruitment in normal and neoplastic human gastric mucosa
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...
Veröffentlicht in: | Clinical immunology (Orlando, Fla.). - 1999. - 118(2006), 1 vom: 01. Jan., Seite 24-34 |
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1. Verfasser: | |
Weitere Verfasser: | , , , , , , , , |
Format: | Aufsatz |
Sprache: | English |
Veröffentlicht: |
2006
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Zugriff auf das übergeordnete Werk: | Clinical immunology (Orlando, Fla.) |
Schlagworte: | Journal Article Research Support, Non-U.S. Gov't Antigens, Surface CXCR3 protein, human Cell Adhesion Molecules Immunoglobulins L-selectin counter-receptors LPL binding proteins, human MADCAM1 protein, human Membrane Proteins mehr... |
Zusammenfassung: | 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. We could detect significantly decreased frequencies of mucosal homing alpha4beta7+ 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 |
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Beschreibung: | Date Completed 03.03.2006 Date Revised 09.12.2020 published: Print-Electronic Citation Status MEDLINE |
ISSN: | 1521-7035 |