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Lydia Visser
PhD

My research in the Pathology department is mainly focused on immunological aspects of B-cell lymphoma. I study interactions of tumor cells with the microenvironment, and signaling pathways in Hodgkin lymphoma and non-Hodgkin lymphomas.

Immune escape mechanisms in Hodgkin’s disease
Background: The nodular sclerosis and mixed cellularity subtypes of Hodgkin’s disease are histologically characterised by a small population of neoplastic cells, the so-called Reed-Sternberg cells and their mononuclear variants (RS cells) and an extensive admixture of other cell types including lymphocytes, plasma cells, eosinophils, and histiocytes. The nature of this infiltrate is largely known, but the mechanisms and functional effects are not. The small lymphocytes immediately surrounding the RS cells are mostly CD4+ T cells that express early activation markers. The absence of prominent specific cytotoxic I cell...
S Poppema, M Potters, L Visser, A. van den Berg
In vitro system for evaluation of the immunomodulatory capacity of CD45(R) reagents
S Poppema, L Visser, X Y Jiang
CD45 (leucocyte common antigen) expression in T and B lymphocyte subsets
Published in: Leukemia and Lymphoma
CD45 is the dominant tyrosine phosphatase in haematopoietic cells and can modulate the effects of many other signaling molecules by dephosphorylation. The extracellular portion of CD45 has considerable variability due to differential splicing and glycosylation. This may allow for interactions with a variety of ligands expressed on interacting cells or on the same cell surface. Monoclonal anti CD45 antibodies that are reactive with epitopes that result from differential splicing and glycosylation can distinguish between cell populations that differ in maturation and function. These reagents can be used in...
S Poppema, R Lai, L Visser, X J Yan
Immunophenotype and functional characteristics of T cells in Hodgkin’s disease
S Poppema, Lydia Visser
Ectopic expression of human and feline CD9 in a human B cell line confers beta 1 integrin-dependent motility on fibronectin and laminin substrates and enhanced tyrosine phosphorylation
Published in: The Journal of Biological Chemistry
Few molecules have been shown to confer cell motility, Although the motility-arresting properties of anti-CD9 monoclonal antibody (mAb) suggest the transmembrane 4 superfamily (TM4SF) member CD9 can induce a motorgenic signal, gene transfection studies have failed to confirm this hypothesis. We report here that ectopic expression of human CD9 (CD9h) and feline CD9 (CD9f) in the CD9-negative, poorly motile, human B cell line Raji dramatically enhances migration across fibronectin- and laminin-coated polycarbonate filters. Migration of Raji/CD9h and Raji/CD9f on either substrate was inhibited by the anti-CDS mAb 50H.19...
A R Shaw, A Domanska, A Mak, A Gilchrist, K Dobler, L Visser, S Poppema, L Fliegel, M Letarte, B J Willett