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10.1371/journal.pone.0174553 http://scihub22266oqcxt.onion/10.1371/journal.pone.0174553 C5391914!5391914!28410377     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=28410377&cmd=llinks): Failed to open stream: HTTP request failed! 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Plasma from patients with anti-glomerular basement membrane disease could recognize microbial peptides |pdf=|usr=}}{{28410377}} gab.com Text Plasma from patients with anti-glomerular basement membrane disease could recognize microbial peptides JO: PLoS One http://www.kidney.de/pget.php?&tw=1&pmid=28410377 #FOAvip Infection has long been suspected as a trigger of autoimmune diseases, and molecular mimicry mechanism was hypothesized in this study. Microbe originated peptides were searched from the Uniprot database based on a previous defined critical amino acid motif within ?3129?150, isoleucine137, tryptophan140, glycine142, phenylalanine 143 and phenylalanine 145. 23826 microbial peptides were identified using our searching strategy, among which seven were related with human infections. Circulating IgG and IgM antibodies against the seven microbial peptides were detected using ELISA in 76 patients with anti-GBM disease. Four peptides were recognized by both IgG and IgM antibodies, and one peptide was recognized by IgG antibodies only. Peptides from Bacteroides, Saccharomyces cerevisiae, and Bifidobacterium thermophilum possessed the highest recognition frequency with the prevalence of 73.7%, 61.8% and 67.1% for IgG, 56.6%, 44.7% and 67.1% for IgM in anti-GBM patients. Patients with antibodies against these microbial peptides showed more severe kidney injury, including higher serum creatinine and higher percentage of crescent formation. In conclusion, antibodies against microbial peptides were identified in the circulation of anti-GBM patients, implying its etiological role in eliciting autoimmune response against ?3(IV)NC1 through molecular mimicry. Twit Text FOAVip Plasma from patients with anti-glomerular basement membrane disease could recognize microbial peptides ????PLoS One http://www.kidney.de/pget.php?&tw=1&pmid=28410377 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=28410377 #FOAvip English Wikipedia <ref>{{Cite pmid|28410377}}</ref> Plasma from patients with anti-glomerular basement membrane disease could recognize microbial peptides #MMPMID28410377 Li Jn; Jia X; Wang Y; Xie C; Jiang T; Cui Z; Zhao Mh PLoS One 2017[]; 12 (4): ä PMID28410377show ga Infection has long been suspected as a trigger of autoimmune diseases, and molecular mimicry mechanism was hypothesized in this study. Microbe originated peptides were searched from the Uniprot database based on a previous defined critical amino acid motif within ?3129?150, isoleucine137, tryptophan140, glycine142, phenylalanine 143 and phenylalanine 145. 23826 microbial peptides were identified using our searching strategy, among which seven were related with human infections. Circulating IgG and IgM antibodies against the seven microbial peptides were detected using ELISA in 76 patients with anti-GBM disease. Four peptides were recognized by both IgG and IgM antibodies, and one peptide was recognized by IgG antibodies only. Peptides from Bacteroides, Saccharomyces cerevisiae, and Bifidobacterium thermophilum possessed the highest recognition frequency with the prevalence of 73.7%, 61.8% and 67.1% for IgG, 56.6%, 44.7% and 67.1% for IgM in anti-GBM patients. Patients with antibodies against these microbial peptides showed more severe kidney injury, including higher serum creatinine and higher percentage of crescent formation. In conclusion, antibodies against microbial peptides were identified in the circulation of anti-GBM patients, implying its etiological role in eliciting autoimmune response against ?3(IV)NC1 through molecular mimicry. äPlasma from patients with anti-glomerular basement membrane disease co(epmc).pdf DeepDyve Pubget Overpricing