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10.1128/JVI.02388-05 http://scihub22266oqcxt.onion/10.1128/JVI.02388-05 16775358!1488968!16775358     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=16775358&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       J+Virol 2006 ; 80 (13): 6697-701 Nephropedia Template TP {{tp|p=16775358|t=2006. A highly restricted T-cell receptor dominates the CD8+ T-cell response to parvovirus B19 infection in HLA-A*2402-positive individuals |pdf=|usr=}}{{16775358}} gab.com Text A highly restricted T-cell receptor dominates the CD8+ T-cell response to parvovirus B19 infection in HLA-A*2402-positive individuals JO: J Virol http://www.kidney.de/pget.php?&tw=1&pmid=16775358 #FOAvip Six of seven HLA-A*2402-positive individuals with acute parvovirus B19 infections made vigorous CD8-positive cytotoxic T-cell (CTL) responses to the viral epitope FYTPLADQF. All responders showed highly focused T-cell receptor (TCR) usage, using almost exclusively BV5.1. The BV5.1 TCR dominated the acute response, was maintained over time, and was also used by a remotely infected individual. Nine CTL clones and two oligoclonal lines obtained from three unrelated individuals used BV5.1, BJ2.1, and a conserved TCR CDR3 of nine amino acids. This commonly recognized epitope is likely important in long-term protective immunity and should be included in vaccine design. Twit Text FOAVip A highly restricted T-cell receptor dominates the CD8+ T-cell response to parvovirus B19 infection in HLA-A*2402-positive individuals ????J Virol http://www.kidney.de/pget.php?&tw=1&pmid=16775358 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=16775358 #FOAvip English Wikipedia <ref>{{Cite pmid|16775358}}</ref> A highly restricted T-cell receptor dominates the CD8+ T-cell response to parvovirus B19 infection in HLA-A*2402-positive individuals #MMPMID16775358 Kasprowicz V; Isa A; Jeffery K; Broliden K; Tolfvenstam T; Klenerman P; Bowness P J Virol 2006[Jul]; 80 (13): 6697-701 PMID16775358show ga Six of seven HLA-A*2402-positive individuals with acute parvovirus B19 infections made vigorous CD8-positive cytotoxic T-cell (CTL) responses to the viral epitope FYTPLADQF. All responders showed highly focused T-cell receptor (TCR) usage, using almost exclusively BV5.1. The BV5.1 TCR dominated the acute response, was maintained over time, and was also used by a remotely infected individual. Nine CTL clones and two oligoclonal lines obtained from three unrelated individuals used BV5.1, BJ2.1, and a conserved TCR CDR3 of nine amino acids. This commonly recognized epitope is likely important in long-term protective immunity and should be included in vaccine design. |CD8-Positive T-Lymphocytes/*immunology/virology[MESH] |Complementarity Determining Regions/genetics/*immunology[MESH] |Epitopes, T-Lymphocyte/*immunology[MESH] |Female[MESH] |HLA-A Antigens/genetics/*immunology[MESH] |HLA-A24 Antigen[MESH] |Humans[MESH] |Male[MESH] |Parvoviridae Infections/genetics/*immunology[MESH] |Parvovirus B19, Human/*immunology[MESH]A highly restricted T-cell receptor dominates the CD8+ T-cell response(epmc).pdf DeepDyve Pubget Overpricing