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10.3389/fimmu.2017.00571 http://scihub22266oqcxt.onion/10.3389/fimmu.2017.00571 C5435753!5435753!28572805     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=28572805&cmd=llinks): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 215 Deprecated: Implicit conversion from float 217.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Front+Immunol 2017 ; 8 (ä): ä Nephropedia Template TP {{tp|p=28572805|t=2017. Factor H Family Proteins in Complement Evasion of Microorganisms |pdf=|usr=}}{{28572805}} gab.com Text Factor H Family Proteins in Complement Evasion of Microorganisms JO: Front Immunol http://www.kidney.de/pget.php?&tw=1&pmid=28572805 #FOAvip Human-pathogenic microbes possess various means to avoid destruction by our immune system. These include interactions with the host complement system that may facilitate pathogen entry into cells and tissues, expression of molecules that defuse the effector complement components and complexes, and acquisition of host complement inhibitors to downregulate complement activity on the surface of the pathogen. A growing number of pathogenic microorganisms have acquired the ability to bind the complement inhibitor factor H (FH) from body fluids and thus hijack its host protecting function. In addition to FH, binding of FH-related (FHR) proteins was also demonstrated for several microbes. Initial studies assumed that these proteins are complement inhibitors similar to FH. However, recent evidence suggests that FHR proteins may rather enhance complement activation both directly and also by competing with the inhibitor FH for binding to certain ligands and surfaces. This mini review focuses on the role of the main alternative pathway regulator FH in host?pathogen interactions, as well as on the emerging role of the FHR proteins as enhancers of complement activation. Twit Text FOAVip Factor H Family Proteins in Complement Evasion of Microorganisms ????Front Immunol http://www.kidney.de/pget.php?&tw=1&pmid=28572805 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=28572805 #FOAvip English Wikipedia <ref>{{Cite pmid|28572805}}</ref> Factor H Family Proteins in Complement Evasion of Microorganisms #MMPMID28572805 Józsi M Front Immunol 2017[]; 8 (ä): ä PMID28572805show ga Human-pathogenic microbes possess various means to avoid destruction by our immune system. These include interactions with the host complement system that may facilitate pathogen entry into cells and tissues, expression of molecules that defuse the effector complement components and complexes, and acquisition of host complement inhibitors to downregulate complement activity on the surface of the pathogen. A growing number of pathogenic microorganisms have acquired the ability to bind the complement inhibitor factor H (FH) from body fluids and thus hijack its host protecting function. In addition to FH, binding of FH-related (FHR) proteins was also demonstrated for several microbes. Initial studies assumed that these proteins are complement inhibitors similar to FH. However, recent evidence suggests that FHR proteins may rather enhance complement activation both directly and also by competing with the inhibitor FH for binding to certain ligands and surfaces. This mini review focuses on the role of the main alternative pathway regulator FH in host?pathogen interactions, as well as on the emerging role of the FHR proteins as enhancers of complement activation. äFactor H Family Proteins in Complement Evasion of Microorganisms (epmc).pdf DeepDyve Pubget Overpricing