z-logo
open-access-imgOpen Access
Associations of Plasma Cytokine and Microbial Translocation Biomarkers With Immune Reconstitution Inflammatory Syndrome
Author(s) -
Varghese George,
Linda Harrison,
Margaret Roach,
Xiaodong Li,
Camlin Tierney,
Margaret A. Fischl,
Judith A. Aberg,
Pablo Tebas,
David M. Asmuth,
Richard B. Pollard,
Catherine Godfrey,
Savita Pahwa
Publication year - 2017
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1093/infdis/jix460
Subject(s) - immune reconstitution inflammatory syndrome , immunology , inflammation , cd14 , immune system , medicine , chromosomal translocation , cxcl10 , biomarker , systemic inflammation , pathogenesis , biology , chemokine , virus , viral load , antiretroviral therapy , gene , biochemistry
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.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom