Non-invasive plasma glycomic and metabolic biomarkers of post-treatment control of HIV.
Leila B GironClovis S PalmerJingjing LiuXiangfan YinEmmanouil PapasavvasRadwa SharafBehzad EtemadMohammad DamraAaron R GoldmanHsin-Yao TangRowena JohnstonKaram MounzerJay R KostmanPablo TebasAlan LandayLuis J MontanerJeffrey M JacobsonJonathan Z LiMohamed Abdel-MohsenPublished in: Nature communications (2021)
Non-invasive biomarkers that predict HIV remission after antiretroviral therapy (ART) interruption are urgently needed. Such biomarkers can improve the safety of analytic treatment interruption (ATI) and provide mechanistic insights into the host pathways involved in post-ART HIV control. Here we report plasma glycomic and metabolic signatures of time-to-viral-rebound and probability-of-viral-remission using samples from two independent cohorts. These samples include a large number of post-treatment controllers, a rare population demonstrating sustained virologic suppression after ART-cessation. These signatures remain significant after adjusting for key demographic and clinical confounders. We also report mechanistic links between some of these biomarkers and HIV latency reactivation and/or myeloid inflammation in vitro. Finally, machine learning algorithms, based on selected sets of these biomarkers, predict time-to-viral-rebound with 74% capacity and probability-of-viral-remission with 97.5% capacity. In summary, we report non-invasive plasma biomarkers, with potential functional significance, that predict both the duration and probability of HIV remission after treatment interruption.
Keyphrases
- antiretroviral therapy
- hiv infected
- hiv positive
- human immunodeficiency virus
- hiv aids
- hiv infected patients
- machine learning
- hiv testing
- hepatitis c virus
- sars cov
- men who have sex with men
- disease activity
- dendritic cells
- bone marrow
- genome wide
- systemic lupus erythematosus
- acute myeloid leukemia
- gene expression
- immune response
- replacement therapy