Abstract

Individuals infected with HIV display varying rates of viral control and disease progression, with a small percentage of individuals being able to spontaneously control infection in the absence of treatment. In attempting to define the correlates associated with natural protection against HIV, extreme heterogeneity in the datasets generated from systems methodologies can be further complicated by the inherent variability encountered at the population, individual, cellular and molecular levels. Furthermore, such studies have been limited by the paucity of well-characterised samples and linked epidemiological data, including duration of infection and clinical outcomes. To address this, we selected 10 volunteers who rapidly and persistently controlled HIV, and 10 volunteers each, from two control groups who failed to control (based on set point viral loads) from an acute and early HIV prospective cohort from East and Southern Africa. A propensity score matching approach was applied to control for the influence of five factors (age, risk group, virus subtype, gender, and country) known to influence disease progression on causal observations. Fifty-two plasma proteins were assessed at two timepoints in the 1st year of infection. We independently confirmed factors known to influence disease progression such as the B*57 HLA Class I allele, and infecting virus Subtype. We demonstrated associations between circulating levels of MIP-1α and IL-17C, and the ability to control infection. IL-17C has not been described previously within the context of HIV control, making it an interesting target for future studies to understand HIV infection and transmission. An in-depth systems analysis is now underway to fully characterise host, viral and immunological factors contributing to control.

Highlights

  • Individuals infected with HIV display varying rates of viral control and disease progression, with a small percentage being able to spontaneously control in vivo viral replication without the need for anti-retroviral treatment (ART) [1]

  • We present the profile for fifty-two soluble proteins in the acute phase of HIV infection across the three groups, demonstrating the potential to identify unique signatures associated with ART-naïve viral control using this selection approach

  • We present a unique approach to classifying individuals drawn from an acute and early HIV infection cohort that considers a range of factors known to have an impact on disease progression, to efficiently define the peripheral secretory profile associated with early and sustained control of in vivo viral replication

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Summary

Introduction

Individuals infected with HIV display varying rates of viral control and disease progression, with a small percentage being able to spontaneously control in vivo viral replication without the need for anti-retroviral treatment (ART) [1]. Such exquisite control is likely to happen in the very early battle between host and virus in acute and early HIV infection [2]. Many of the studies of HIV control are cross-sectional after set point viral load and control has been achieved. A full understanding of the mechanisms governing such spontaneous control of infection has been hampered by the paucity of informative and linked samples coupled to technology with sufficient resolution to define this phenomenon

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