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Interleukin (IL)‐10 has been implicated in persistence of pathogens in a number of chronic infections. Infected CD4+ cells upon reactivation with HIV antigens were also shown to produce IL‐10, which might contribute to their persistence. Hence, it is crucial to determine mechanisms regulating IL‐10 production after activation with HIV antigens for devising effective blocking strategies. In this study, ERK‐, T‐bet‐ and FoxP3‐dependent pathways were evaluated for their possible roles in IL‐10 production by infected CD4+ cells after reactivation with HIV Env. Intracellular and secreted IL‐10 levels were determined by flow cytometry and Bioplex assay after treating PBMCs with PD98059, tipifarnib and cyclosporin A for blocking of ERK‐, T‐bet‐and FoxP3‐dependent pathways, respectively. Baseline levels of T‐bet, pERK were higher in P24+ CD4+ cells as compared to uninfected CD4+ cells, which increased further after activation with Env. Inhibition of T‐bet resulted in 2.3‐fold reduction of IL‐10 expression whereas ERK and FoxP3 inhibition failed to cause suppression of IL‐10 expression. Conversely, IL‐10 secreted by PBMCs was inhibited maximally after ERK inhibition suggesting its role in regulation of cytokine secretory pathway. IFN‐γ was found to be suppressed after treatment with inhibitors of all these pathways. Thus, the study highlighted need for IL‐10 blockade along with the use of antigens for therapeutic vaccinations or latency reversal and identified the T‐bet‐dependent pathway as an important pathway regulating IL‐10 production by infected CD4+ cells. However, simultaneous blockade of IFN‐γ precludes use of inhibitor of this pathway as an IL‐10 blocking strategy.  相似文献   
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2D echocardiography was performed on a 4-year-old child suffering from right thigh abscess due to MRSA infection following diagnosis of pericardial effusion by USG abdomen. It revealed myocardial abscess and pericardial effusion. This child underwent series of 2D echocardiographic studies which showed image appearance of myocardial abscess with its time course of healing.  相似文献   
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In India transmission of transfusion transmissible infections (TTI) has shown a relative decrease as a result of mandatory screening of donated blood for TTI’s. However, reducing the incidence of non infectious complications poses a major challenge, mainly due to the fact that a number of adverse reactions go unreported. Blood transfusion reaction, can be categorized based on the time interval between transfusion of blood products and the presentation of adverse reactions as acute i.e. those presenting during or within 24 h and as delayed i.e. those presenting anytime after 24 h. Transfusion reactions can further be classified as immune and non immune or infectious and non infectious based on the pathophysiology. In this retrospective study which was undertaken with an aim to determine the type and frequency of non infectious complications due to transfusion of blood and blood products recorded the incidence of febrile non hemolytic transfusion reactions (FNHTR) 51.40 %, allergic reactions 40.14 %, non immune hemolytic reactions 4.22 %, hypothermia 2.81 %, anaphylaxis 0.70 % and iron overload 0.70 %. FNHTR which was found to be the most common complication in this study can certainly be minimized, if not completely eliminated by adopting a policy of universal leucodepletion, the implementation of which solely depends on the financial and infrastructure resources available. This study also reiterates the importance of hemovigilance as a tool to improve the safety of blood transfusion.  相似文献   
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