{"id":343280,"date":"2016-12-29T15:46:36","date_gmt":"2016-12-29T23:46:36","guid":{"rendered":"https:\/\/cm-edgetun.pages.dev\/en-us\/research\/?post_type=msr-research-item&#038;p=343280"},"modified":"2018-10-16T21:37:59","modified_gmt":"2018-10-17T04:37:59","slug":"nef-mediated-regulation-cd4-hla-class-hiv-1-subtype-c-infection-association-disease-progression-influence-immune-pressure","status":"publish","type":"msr-research-item","link":"https:\/\/cm-edgetun.pages.dev\/en-us\/research\/publication\/nef-mediated-regulation-cd4-hla-class-hiv-1-subtype-c-infection-association-disease-progression-influence-immune-pressure\/","title":{"rendered":"Nef-mediated down-regulation of CD4 and HLA class I in HIV-1 subtype C infection: Association with disease progression and influence of immune pressure"},"content":{"rendered":"<div class=\"abstract svAbstract \" data-etype=\"ab\">\n<p id=\"sp0050\">Nef plays a major role in HIV-1 pathogenicity. We studied HIV-1 subtype C infected individuals in acute\/early (<em>n<\/em>=120) or chronic (<em>n<\/em>=207) infection to investigate the relationship between Nef-mediated CD4\/HLA-I down-regulation activities and disease progression, and the influence of immune-driven sequence variation on these Nef functions. A single Nef sequence per individual was cloned into an expression plasmid, followed by transfection of a T cell line and measurement of CD4 and HLA-I expression. In early infection, a trend of higher CD4 down-regulation ability correlating with higher viral load set point was observed (<em>r<\/em>=0.19, <em>p<\/em>=0.05), and higher HLA-I down-regulation activity was significantly associated with faster rate of CD4 decline (<em>p<\/em>=0.02). HLA-I down-regulation function correlated inversely with the number HLA-associated polymorphisms previously associated with reversion in the absence of the selecting HLA allele (<em>r<\/em>=\u22120.21, <em>p<\/em>=0.0002). These data support consideration of certain Nef regions in HIV-1 vaccine strategies designed to attenuate the infection course.<\/p>\n<\/div>\n","protected":false},"excerpt":{"rendered":"<p>Nef plays a major role in HIV-1 pathogenicity. We studied HIV-1 subtype C infected individuals in acute\/early (n=120) or chronic (n=207) infection to investigate the relationship between Nef-mediated CD4\/HLA-I down-regulation activities and disease progression, and the influence of immune-driven sequence variation on these Nef functions. A single Nef sequence per individual was cloned into an 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