Associations of plasma cytokine and microbial translocation biomarkers with immune reconstitution inflammatory syndrome

V George, L Harrison, M Roach, XD Li… - The Journal of …, 2017 - academic.oup.com
V George, L Harrison, M Roach, XD Li, C Tierney, MA Fischl, J Aberg, P Tebas, DM Asmuth…
The Journal of infectious diseases, 2017academic.oup.com
A nested case-cohort study was performed in participants of a clinical trial of first-line human
immunodeficiency virus treatments to investigate plasma biomarkers of inflammation and
microbial translocation for their association with immune reconstitution inflammatory
syndrome (IRIS). Fifty-one of 1452 participants with baseline CD4 count< 350 cells/μL
developed IRIS. Plasma from 51 IRIS cases, including 6 stratified by preenrollment CD4
count≤ 200 cells/μL, were analyzed and compared to 94 non-IRIS controls. At baseline …
Abstract
A nested case-cohort study was performed in participants of a clinical trial of first-line human immunodeficiency virus treatments to investigate plasma biomarkers of inflammation and microbial translocation for their association with immune reconstitution inflammatory syndrome (IRIS). Fifty-one of 1452 participants with baseline CD4 count <350 cells/μL developed IRIS. Plasma from 51 IRIS cases, including 6 stratified by preenrollment CD4 count ≤200 cells/μL, were analyzed and compared to 94 non-IRIS controls. At baseline, CXCL10, lipopolysaccharide, soluble CD14, 16S ribosomal DNA, and interferon-α2 were associated with greater risk of IRIS. Systemic inflammation through persistent monocyte activation and microbial translocation appear to be important in IRIS pathogenesis.
Oxford University Press