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• W2000902524 abstract "B-cell receptor (BCR) and Toll-like receptor (TLR) stimulation and integration with signals from the pathogen or immune cells and their products determine the B-cell antibody response. Low expression of BCR is the hallmark of B lymphocytes in CLL, however little is known about the expression and function of TLR in B-CLL. We studied TLR2, TLR4, IL-6 and mIL-6Rα expression on mRNA and protein level in CD19+ subpopulation of normal lymphocytes and the CD19+CD5+ subpopulation from B-CLL. Experiments were performed on unstimulated and stimulated lymphocytes [Staphylococcus aureus Cowan I (SAC) and lipopolysaccharide (LPS) from Escherichia coli — TLR2- and TLR4-specific agonists, respectively]. We showed undetectable or low IL-6 expression, which seems to be specific for B-CLL lymphocytes. Induction of TLR4 mRNA upon LPS stimulation affected the expression of IL-6, but not of mIL-6Rα. Increased expression of TLR2 (MFI) after LPS and SAC stimulation did not correlate with mIL-6Rα receptor expression. B-CLL CD19+CD5+ lymphocytes showed a significant increase in TLR2 expression at the protein level after stimulation with SAC and LPS compared to normal CD19+ lymphocytes. TLR2 may influence the behaviour of the malignant clone in B-CLL." @default.
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• W2000902524 date "2012-06-01" @default.
• W2000902524 modified "2023-10-06" @default.
• W2000902524 title "TLR2 may influence the behavior of the malignant clone in B-CLL" @default.
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• W2000902524 doi "https://doi.org/10.1016/j.bcmd.2012.03.006" @default.
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