However, as anticipated, there was a highly significant correlation between IFABP and LBP ( Supplementary Figure 2B ) associated with the increase in inflammaging phenotype during the chronic phase of treated SIV infection.
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Dysregulation of IL-17/IL-22 Effector Functions in Blood and Gut Mucosal Gamma Delta T Cells Correlates With Increase in Circulating Leaky Gut and Inflammatory Markers During cART-Treated Chronic SIV Infection in Macaques.
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