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10.1111/imm.12504 http://scihub22266oqcxt.onion/10.1111/imm.12504 26173489!4693898!26173489     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=26173489&cmd=llinks): Failed to open stream: HTTP request failed! 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Contribution of dendritic cells to the autoimmune pathology of systemic lupus erythematosus |pdf=|usr=}}{{26173489}} gab.com Text Contribution of dendritic cells to the autoimmune pathology of systemic lupus erythematosus JO: Immunology http://www.kidney.de/pget.php?&tw=1&pmid=26173489 #FOAvip Systemic lupus erythematosus (SLE) is a heterogeneous disease in which excessive inflammation, autoantibodies and complement activation lead to multisystem tissue damage. The contribution of the individual genetic composition has been extensively studied, and several susceptibility genes related to immune pathways that participate in SLE pathogenesis have been identified. It has been proposed that SLE takes place when susceptibility factors interact with environmental stimuli leading to a deregulated immune response. Experimental evidence suggests that such events are related to the failure of T-cell and B-cell suppression mediated by defects in cell signalling, immune tolerance and apoptotic mechanism promoting autoimmunity. In addition, it has been reported that dendritic cells (DCs) from SLE patients, which are crucial in the modulation of peripheral tolerance to self-antigens, show an increased ratio of activating/inhibitory receptors on their surfaces. This phenotype and an augmented expression of co-stimulatory molecules is thought to be critical for disease pathogenesis. Accordingly, tolerogenic DCs can be a potential strategy for developing antigen-specific therapies to reduce detrimental inflammation without causing systemic immunosuppression. In this review article we discuss the most relevant data relative to the contribution of DCs to the triggering of SLE. Twit Text FOAVip Contribution of dendritic cells to the autoimmune pathology of systemic lupus erythematosus ????Immunology http://www.kidney.de/pget.php?&tw=1&pmid=26173489 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=26173489 #FOAvip English Wikipedia <ref>{{Cite pmid|26173489}}</ref> Contribution of dendritic cells to the autoimmune pathology of systemic lupus erythematosus #MMPMID26173489 Mackern-Oberti JP; Llanos C; Riedel CA; Bueno SM; Kalergis AM Immunology 2015[Dec]; 146 (4): 497-507 PMID26173489show ga Systemic lupus erythematosus (SLE) is a heterogeneous disease in which excessive inflammation, autoantibodies and complement activation lead to multisystem tissue damage. The contribution of the individual genetic composition has been extensively studied, and several susceptibility genes related to immune pathways that participate in SLE pathogenesis have been identified. It has been proposed that SLE takes place when susceptibility factors interact with environmental stimuli leading to a deregulated immune response. Experimental evidence suggests that such events are related to the failure of T-cell and B-cell suppression mediated by defects in cell signalling, immune tolerance and apoptotic mechanism promoting autoimmunity. In addition, it has been reported that dendritic cells (DCs) from SLE patients, which are crucial in the modulation of peripheral tolerance to self-antigens, show an increased ratio of activating/inhibitory receptors on their surfaces. This phenotype and an augmented expression of co-stimulatory molecules is thought to be critical for disease pathogenesis. Accordingly, tolerogenic DCs can be a potential strategy for developing antigen-specific therapies to reduce detrimental inflammation without causing systemic immunosuppression. In this review article we discuss the most relevant data relative to the contribution of DCs to the triggering of SLE. |*Autoimmunity[MESH] |Animals[MESH] |Antigen-Antibody Complex/immunology[MESH] |B-Lymphocytes/immunology/metabolism[MESH] |Cell Communication/immunology[MESH] |Dendritic Cells/drug effects/*immunology/metabolism[MESH] |Disease Models, Animal[MESH] |Humans[MESH] |Immune Tolerance[MESH] |Immunologic Factors/immunology/metabolism[MESH] |Immunomodulation[MESH] |Immunophenotyping[MESH] |Interferon-alpha/metabolism[MESH] |Lupus Erythematosus, Systemic/drug therapy/*immunology/metabolism[MESH] |Mice[MESH] |Phenotype[MESH] |Receptors, Pattern Recognition/metabolism[MESH]Contribution of dendritic cells to the autoimmune pathology of systemi(epmc).pdf DeepDyve Pubget Overpricing