High Plasma Levels of sTNF-R1 and CCL11 Are Related to CD4+ T-Cells Fall in Human Immunodeficiency Virus Elite Controllers With a Sustained Virologic Control.

ABSTRACT: Our aim was to analyze the relationship between plasma inflammatory biomarkers and CD4+ T-cells evolution in human immunodeficiency virus (HIV) elite controllers (HIV-ECs) with a suppressed viremia. We carried out a retrospective study in 30 HIV-ECs classified into two groups: those showing no significant loss of CD4+ T-cells during the observation period (stable CD4+, n?=?19) and those showing a significant decrease of CD4+ T-cells (decline CD4+, n?=?11). Baseline plasma biomarkers were measured using a multiplex immunoassay: sTNF-R1, TRAIL, sFas (APO), sFasL, TNF-?, TNF-?, IL-8, IL-18, IL-6, IL-10, IP-10, MCP-1, MIP-1?, MIP-1?, RANTES, SDF1?, GRO-?, and CCL11. Baseline levels of sTNF-R1 and CCL11 and sTNF-R1/TNF-? ratio correlated with the slope of CD4+ T-cells (cells/?l/year) during follow-up [r?=?-0.370 (p?=?0.043), r?=?-0.314 (p?=?0.091), and r?=?-0.381 (p?=?0.038); respectively]. HIV-ECs with declining CD4+ T-cells had higher baseline plasma levels of sTNF-R1 [1,500.7 (555.7; 2,060.7) pg/ml vs. 450.8 (227.9; 1,263.9) pg/ml; p?=?0.018] and CCL11 [29.8 (23.5; 54.9) vs. 19.2 (17.8; 29.9) pg/ml; p?=?0.041], and sTNF-R1/TNF-? ratio [84.7 (33.2; 124.2) vs. 25.9 (16.3; 75.1); p?=?0.012] than HIV-1 ECs with stable CD4+ T-cells. The area under the receiver operating characteristic (ROC) curve [area under ROC curve (AUROC)] were 0.758?±?0.093 (sTNF-R1), 0.727?±?0.096 (CCL11), and 0.777?±?0.087 (sTNF-R1/TNF-?). The cut-off of 75th percentile (high values) for these biomarkers had 71.4% positive predictive value and 73.9% negative predictive value for anticipating the evolution of CD4+ T-cells. In conclusion, the loss of CD4+ T-cells in HIV-ECs was associated with higher levels of two plasma inflammatory biomarkers (sTNF-R1 and CCL11), which were also reasonably accurate for the prediction of the CD4+ T-cells loss.

SUBMITTER: Gutierrez-Rivas M 

PROVIDER: S-EPMC6015886 | biostudies-literature | 2018

REPOSITORIES: biostudies-literature