Please use this identifier to cite or link to this item: https://www.um.edu.mt/library/oar/handle/123456789/12169
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dc.contributor.authorFormosa, Norman-
dc.contributor.authorSaliba, Christian-
dc.contributor.authorBaldacchino, Shawn-
dc.contributor.authorCamilleri, David J.-
dc.contributor.authorGrech, Godfrey-
dc.date.accessioned2016-09-02T09:51:58Z-
dc.date.available2016-09-02T09:51:58Z-
dc.date.issued2016-
dc.identifier.citationGrech, G., Baldacchino S., Camilleri, D.J., Formosa, N. & Saliba, S. (2016). The re-emergence of the B1 cell compartment : is this a pre-lymphoma stage?. Xjenza, 4(1), 11-17en_GB
dc.identifier.urihttps://www.um.edu.mt/library/oar//handle/123456789/12169-
dc.description.abstractChronic Lymphocytic Leukemia (CLL) are in some cases stereotyped for immunoglobulin variants in different populations, suggesting emergence of B cell subsets following presentation of the same antigen. CLL cells may originate from CD5+ naïve cells and from CD5 memory cells. Gene expression studies characterized a common cell of origin of the two clinical categories of CLL; the unmutated aggressive type and the mutated indolent type. The aim of this study was to investigate the presence of CD5 positive B cells in the elderly and their potential stimulation with exosomes derived from tumor cells. The findings from this study is aimed to create a model to identify instigating carcinomatous factors that may stimulate B1 cells to transform into a CLL-like model. In this study we show that CD19\textsuperscript+ cells (B cells) in cord blood have a high expression of CD5. CD19/CD5 staining of blood samples from senior citizens showed the presence of B cells which also express the CD5 marker, though at a lower expression when compared to CLL cells (CD19+/CD5 dim B cells). Measurement of clonality using λ/Κ flow cytometry staining show a monoclonal origin of the human CD19+/CD5 dim B cells. Monoclonal B cell Lymphocytosis in the elderly is a potential cell compartment that represents the origin of B cell proliferative disorders. The origin of the B cell proliferative disease requires antigen stimulation. A preliminary experiment showed that sorted lymphocytes can be stimulated by exosomes isolated from 2 cancer cells lines, A549 (lung epithelial) and PC3 (prostate cell line). In comparison with phytohaemagglutinin (PHA) and phorbolmyristate acetate (PMA), known lymphocyte stimulators, the exosomes stimulated the proliferation of monocytic-like cells. Further characterization is required to know the origin of these cells. The result shows that one can speculate that exosomes present cancer-derived antigens and stimulate cell proliferation. Further studies are required to evaluate the potential transformation capacity of cancer-derived exosomes. In addition, various cytokines were measured in the sera of senior citizens to investigate a differential release of cytokines in the presence or absence of the CD19+/CD5 dim B cells. Cytokines examined were not significantly different between the 2 groups and further evaluation of cytokine levels is required.en_GB
dc.language.isoenen_GB
dc.publisherMalta Chamber of Scientistsen_GB
dc.rightsinfo:eu-repo/semantics/openAccessen_GB
dc.subjectB-Lymphocyte subsetsen_GB
dc.subjectLymphocytosisen_GB
dc.subjectChronic lymphocytic leukemiaen_GB
dc.subjectLeukemia, Lymphocytic, Chronic, B-Cellen_GB
dc.titleThe re-emergence of the B1 cell compartment : is this a pre-lymphoma stage?en_GB
dc.typearticleen_GB
dc.rights.holderThe copyright of this work belongs to the author(s)/publisher. The rights of this work are as defined by the appropriate Copyright Legislation or as modified by any successive legislation. Users may access this work and can make use of the information contained in accordance with the Copyright Legislation provided that the author must be properly acknowledged. Further distribution or reproduction in any format is prohibited without the prior permission of the copyright holder.en_GB
dc.description.reviewedpeer-revieweden_GB
dc.identifier.doi10.7423/XJENZA.2016.1.02-
Appears in Collections:Scholarly Works - FacM&SPat
Scholarly Works - FacM&SSur
Xjenza, 2016, Volume 4, Issue 1
Xjenza, 2016, Volume 4, Issue 1

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