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Contribution of intestinal barrier damage, microbial translocation and HIV-1 infection status to an inflammaging signature

Systemic inflammation is a characteristic of both HIV-1 infection and aging ("inflammaging"). Intestinal epithelial barrier damage (IEBD) and microbial translocation (MT) contribute to HIV-associated inflammation, but their impact on inflammaging remains unclear. Plasma biomarkers for IEBD...

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Bibliographic Details
Published in:PloS one 2014-05, Vol.9 (5), p.e97171-e97171
Main Authors: Steele, Amanda K, Lee, Eric J, Vestal, Brian, Hecht, Daniel, Dong, Zachary, Rapaport, Eric, Koeppe, John, Campbell, Thomas B, Wilson, Cara C
Format: Article
Language:English
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Summary:Systemic inflammation is a characteristic of both HIV-1 infection and aging ("inflammaging"). Intestinal epithelial barrier damage (IEBD) and microbial translocation (MT) contribute to HIV-associated inflammation, but their impact on inflammaging remains unclear. Plasma biomarkers for IEBD (iFABP), MT (LPS, sCD14), T-cell activation (sCD27), and inflammation (hsCRP, IL-6) were measured in 88 HIV-1 uninfected (HIV(neg)) and 83 treated, HIV-1-infected (HIV(pos)) adults from 20-100 years old. Age positively correlated with iFABP (r = 0.284, p = 0.008), sCD14 (r = 0.646, p = 
ISSN:1932-6203
1932-6203
DOI:10.1371/journal.pone.0097171