This is consistent with previous findings, which demonstrated that DENV-infected monocytes stimulated B cell differentiation into plasmablasts [41]. Open in a separate window Fig 7 Purified B cells cultured with dengue virus showed increased expression of costimulatory AGN 195183 molecules.B lymphocytes were mock-treated Rabbit Polyclonal to E2F4 or cultured with DENV2 (MOI = 1) for the indicated time points and the expression of CD86 (A) or HLA-DR (B) in CD19+ cells were evaluated by flow cytometry. 48h p.i., and the expression of phosphotyrosine were analyzed in the cell lysates by western blotting. The cells were also stained with anti-actin antibody as a loading control. B) The cells were harvested after 2h or 48h p.i., and the expression of AGN 195183 phosphorylated (pAKT) or unphosphorylated AKT (AKT) were analyzed in the cell lysates by western blotting, using the indicated antibodies. Bars indicate the ratio between the analyzed phosphorylated protein and the corresponding unphosphorylated one. Data are representative of two independent experiments.(TIF) pone.0143391.s003.tif (97K) GUID:?BC34DBCB-B19D-49B2-B8AF-4DCB47517483 S4 Fig: Evaluation of the cytotoxicity of anti-CD81 and MAPK inhibitors in B cell cultures. A) B lymphocytes were cultured with DENV2 (MOI = 1) in the presence or absence of ERK (PD98059), p38 (SB203580) and JNK (SP600125) inhibitors, or anti-CD81 antibody. After 72h, the cells were incubated with PI and analyzed by flow cytometry. B) B lymphocytes were cultured with anti-CD81 antibody at different concentrations and, after 72h, cell viability was evaluated by XTT assay. C) B cells were mock-treated or cultured with DENV in the presence or absence of anti-CD81. After 72h, the supernatants were harvested and the amount of released lactated dehydrogenase (LDH) was evaluated, as described.(TIF) pone.0143391.s004.tif (158K) GUID:?FDD90790-1483-4C2B-AE0A-6D36560A226D Data Availability StatementAll relevant data are within the paper and its Supporting Information files. Abstract Dengue infection is associated to vigorous inflammatory response, to a high frequency of activated B cells, and to increased levels of circulating cross-reactive antibodies. We investigated whether direct infection of B cells would promote activation by culturing primary human B lymphocytes from healthy donors with DENV might promote Ig isotype switching and IgG secretion from different B cell clones. These findings suggest that activation signaling pathways triggered by DENV interaction with non-specific receptors on B cells might contribute to the exacerbated response observed in dengue patients. Introduction Dengue viruses (DENV) belong to the family and comprise four genetically distinct serotypes (DENV1-DENV4), responsible for AGN 195183 millions of infections each year in tropical and subtropical areas of the world. According to the World Health Organization dengue incidence has highly increased over the past 50 years, turning this infection the most important arthropod-born disease in the world and a global health challenge [1, 2]. Dengue infection causes clinical manifestations ranging from mild to severe symptoms associated to fever, hemorrhagic manifestations, increased vascular permeability and plasma leakage, and may be a AGN 195183 life threatening disease [3, 4]. Severe dengue is more common in secondary infections and it has been suggested that the activation of low-affinity cross-neutralizing T and/or B cells, and an exacerbated inflammatory response are correlated to disease severity [5, 6, 7, 8]. The most widely supported theory proposed to explain the increased risk of severe dengue is antibody dependent enhancement (ADE), which postulates that antibodies from previous heterologous infection are cross-reactive and poorly neutralize the circulating virus in a secondary episode [4, 9]. The immune complexes generated by these antibodies would then facilitate virus entry in FcR-bearing cells [10, 11]. In fact, a large fraction of antibodies generated during both primary and secondary infections are serotype cross-reactive and non-neutralizing, indicating that antibody response during dengue infection is very complex and may either benefit or harm the patient [12, 13, 14, 15, 16]. Activation of B lymphocytes may be triggered by antigen-specific BCR activation and/or by other polyclonally distributed receptors, including pathogen recognition receptors (PRRs), B cell coreceptor complex, and costimulatory receptors (e.g. CD40, BAFFR, among others). Effective antibody response depends on the integration of multiple signals that converge at the level of transcription factor activation, and induces B cell proliferation and differentiation into effector plasma cells or long lived memory B cells [17, 18, 19, 20, 21, 22]. Mitogen-activated protein kinases (MAPK), including extracellular signal-regulated kinase (ERK), c-Jun NH2-terminal kinase (JNK/SAPK) and p38 MAPK, are downstream mediators of transmission transduction pathways targeted by some of the cited receptors, and their activation influence on nuclear translocation of.
This is consistent with previous findings, which demonstrated that DENV-infected monocytes stimulated B cell differentiation into plasmablasts [41]