1999
DOI: 10.1016/s0016-5085(99)70395-1
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Impaired T-cell regulation of B-cell growth in Helicobacter pylori–related gastric low-grade MALT lymphoma

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Cited by 100 publications
(85 citation statements)
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“…In addition to promoting the proliferation and differentiation of malignant B-cell clones, tumor-infiltrating T-cells in lowgrade gastric MALT lymphomas are found to be defective in both perforin-mediated cytotoxicity and Fas-Fas ligand mediated apoptosis [28] . On the other hand, the tumor tissues of high-grade MALT lymphomas appear to contain a much higher number of apoptotic lymphoma cells and CD8+ cytotoxic T lymphocytes (CTLs) [21] .…”
Section: Discussionmentioning
confidence: 99%
“…In addition to promoting the proliferation and differentiation of malignant B-cell clones, tumor-infiltrating T-cells in lowgrade gastric MALT lymphomas are found to be defective in both perforin-mediated cytotoxicity and Fas-Fas ligand mediated apoptosis [28] . On the other hand, the tumor tissues of high-grade MALT lymphomas appear to contain a much higher number of apoptotic lymphoma cells and CD8+ cytotoxic T lymphocytes (CTLs) [21] .…”
Section: Discussionmentioning
confidence: 99%
“…T cell blasts from each clone were cocultured with 51 Cr-labeled Jurkat cells at an effector͞ target ratio of 10, 5, and 2.5 to 1 for 18 h in the presence of phorbol-12-myristate-13-acetate (10 ng͞ml) and ionomycin (1 mmol͞l), as reported (18). To block Fas-Fas ligand interaction, the anti-Fas antagonistic monoclonal antibody M3 (Immunex) was used at a 5 g͞ml final concentration in a 30-min pretreatment of 51 Cr-labeled Jurkat cells, as reported (22).…”
Section: Methodsmentioning
confidence: 99%
“…T cell blasts from each clone were co-cultured with 51 Cr-labeled Jurkat cells at eVector to target ratios of 10, 5, and 2.5-1 for 18 h in the presence of PMA (10 ng/ml) and ionomycin (1 mmol/l), as reported [4]. To block Fas-FasL interaction, the anti-Fas antagonistic monoclonal antibody M3 (Amgen, Thousand Oaks, USA) was used at a 5 g/ml Wnal concentration in a 30-min pretreatment of 51 Cr-labeled Jurkat cells, as reported [3].…”
Section: Perforin-mediated Cytotoxicity and Fas-fas Ligand(l)-mediatementioning
confidence: 99%
“…Since most of antigen-activated Th1 and Th0 clones express perforin-mediated cytotoxicity against autologous antigen-presenting APC (e.g., GCAA peptidepulsed B cells) [3], we assessed the cytolytic potential of peptide-speciWc T cell clones using GCAA peptide-pulsed 51 Cr-labeled autologous EBV-B cells as targets. At an eVector to target ratio of 10:1, all 50 CD4 + Th1 and 11 out of the 15 Th0 CD4 + clones lysed GCAA peptide-presenting autologous EBV-B cells (Fig.…”
Section: Gcaa Peptide-speciwc T Cells Inwltrate the Neoplastic Tissuementioning
confidence: 99%