1998European Journal of Gastroenterology & HepatologyRequires access

CD4+CD8+ and CD8α+β- T lymphocytes in human small intestinal lamina propria

Mohamed Abuzakouk, Janet Carton, Conleth Feighery, Diarmuid P. OʼDonoghue, Donald G. Weir, Cliona O’Farrelly

Open publisher page 33 citations

Abstract

OBJECTIVE: To examine CD8 expression by T-lymphocyte subpopulations from disease-free human lamina propria. METHODS: Single-cell suspensions were prepared from the epithelial layer and the lamina propria of small intestinal biopsies obtained endoscopically from disease-free patients. Monoclonal antibodies against CD3, CD4, CD8, CD56, CD8alphabeta, CD8alpha, TCR alphabeta and TCR gammadelta were used for dual and three-colour flow cytometric analysis. RESULTS: In addition to classical CD4+ and CD8+ T lymphocytes a substantial proportion of lamina propria T lymphocytes were CD4+ CD8+ or 'double positive' (mean 14%, range 4-26%). This population was significantly lower in the epithelial layer of the same patients (mean 7%, range 3-21%, P < 0.007). Three-colour flow cytometric analysis revealed that expression of the CD8 molecule on double positive T cells in the lamina propria was limited to the CD8alpha chain. Furthermore, of the CD8+ population, CD8+ T cells which only expressed the alpha chain were present in greater numbers in the lamina propria (mean 35%, range 14-54%) than in the epithelial layer (mean 18%, range 5-37%, P < 0.02). NK (CD56+) cells were not detected and few gammadeltaTCR+ T lymphocytes were detected in the lamina propria (mean 2%, range 0.5-6.6%) when compared with the epithelial layer (mean 8%, range 0.2-14%, P < 0.008). CONCLUSION: A significant population of CD4+ CD8alpha+ T lymphocytes which are CD8beta chain negative have been detected in the intestinal lamina propria. These cells form a more significant component of the lamina propria than the epithelial layer T-cell repertoire and may have a unique function in intestinal immunoregulation.

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OBJECTIVE: To examine CD8 expression by T-lymphocyte subpopulations from disease-free human lamina propria. METHODS: Single-cell suspensions were prepared from the epithelial layer and the lamina propria of small intestinal biopsies obtained endoscopically from disease-free patients. Monoclonal antibodies against CD3, CD4, CD8, CD56, CD8alphabeta, CD8alpha, TCR alphabeta and TCR gammadelta were used for dual and three-colour flow cytometric analysis. RESULTS: In addition to classical CD4+ and CD8+ T lymphocytes a substantial proportion of lamina propria T lymphocytes were CD4+ CD8+ or 'double positive' (mean 14%, range 4-26%). This population was significantly lower in the epithelial layer of the same patients (mean 7%, range 3-21%, P < 0.007). Three-colour flow cytometric analysis revealed that expression of the CD8 molecule on double positive T cells in the lamina propria was limited to the CD8alpha chain. Furthermore, of the CD8+ population, CD8+ T cells which only expressed the alpha chain were present in greater numbers in the lamina propria (mean 35%, range 14-54%) than in the epithelial layer (mean 18%, range 5-37%, P < 0.02). NK (CD56+) cells were not detected and few gammadeltaTCR+ T lymphocytes were detected in the lamina propria (mean 2%, range 0.5-6.6%) when compared with the epithelial layer (mean 8%, range 0.2-14%, P < 0.008). CONCLUSION: A significant population of CD4+ CD8alpha+ T lymphocytes which are CD8beta chain negative have been detected in the intestinal lamina propria. These cells form a more significant component of the lamina propria than the epithelial layer T-cell repertoire and may have a unique function in intestinal immunoregulation.

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Available abstract

OBJECTIVE: To examine CD8 expression by T-lymphocyte subpopulations from disease-free human lamina propria. METHODS: Single-cell suspensions were prepared from the epithelial layer and the lamina propria of small intestinal biopsies obtained endoscopically from disease-free patients. Monoclonal antibodies against CD3, CD4, CD8, CD56, CD8alphabeta, CD8alpha, TCR alphabeta and TCR gammadelta were used for dual and three-colour flow cytometric analysis. RESULTS: In addition to classical CD4+ and CD8+ T lymphocytes a substantial proportion of lamina propria T lymphocytes were CD4+ CD8+ or 'double positive' (mean 14%, range 4-26%). This population was significantly lower in the epithelial layer of the same patients (mean 7%, range 3-21%, P < 0.007). Three-colour flow cytometric analysis revealed that expression of the CD8 molecule on double positive T cells in the lamina propria was limited to the CD8alpha chain. Furthermore, of the CD8+ population, CD8+ T cells which only expressed the alpha chain were present in greater numbers in the lamina propria (mean 35%, range 14-54%) than in the epithelial layer (mean 18%, range 5-37%, P < 0.02). NK (CD56+) cells were not detected and few gammadeltaTCR+ T lymphocytes were detected in the lamina propria (mean 2%, range 0.5-6.6%) when compared with the epithelial layer (mean 8%, range 0.2-14%, P < 0.008). CONCLUSION: A significant population of CD4+ CD8alpha+ T lymphocytes which are CD8beta chain negative have been detected in the intestinal lamina propria. These cells form a more significant component of the lamina propria than the epithelial layer T-cell repertoire and may have a unique function in intestinal immunoregulation.

Key concepts: Lamina propria, CD8, Population, Biology, Molecular biology, Cytotoxic T cell, CD3, Immunology

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