4.6 Article

Transient Increases in Inflammation and Proapoptotic Potential Are Associated with the HESN Phenotype Observed in a Subgroup of Kenyan Female Sex Workers

Journal

VIRUSES-BASEL
Volume 14, Issue 3, Pages -

Publisher

MDPI
DOI: 10.3390/v14030471

Keywords

HIV-1; HESN; ISG; PBMC; IFN-gamma; antiviral; commercial sex workers

Categories

Funding

  1. Canadian Institutes of Health Research (CIHR) [154043]
  2. Yangquan Municipal Center for Disease Prevention and Control, China

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In a group of Kenyan female sex workers who remain seronegative despite repeated exposure to HIV-1, a unique profile of proinflammatory and proapoptotic ISGs with robust but transient responses to exogenous IFN was identified. The HESN cells also showed increased expression of negative regulators of ISG induction, potentially contributing to a strict regulation of ISG expression and decreased HIV susceptibility. The distinct ISG profile in HESN cells may be a correlate of protection against HIV infection.
Interferon (IFN) -stimulated genes (ISGs) are critical effectors of IFN response to viral infection, but whether ISG expression is a correlate of protection against HIV infection remains elusive. A well-characterized subcohort of Kenyan female sex workers, who, despite being repeatedly exposed to HIV-1 remain seronegative (HESN), exhibit reduced baseline systemic and mucosal immune activation. This study tested the hypothesis that regulation of ISGs in the cells of HESN potentiates a robust antiviral response against HIV. Transcriptional profile of a panel of ISGs with antiviral function in PBMC and isolated CD4+ T cells from HESN and non-HESN sex worker controls were defined following exogenous IFN-stimulation using relative RT-qPCR. This study identified a unique profile of proinflammatory and proapoptotic ISGs with robust but transient responses to exogenous IFN-gamma and IFN-alpha 2 in HESN cells. In contrast, the non-HESN cells had a strong and prolonged proinflammatory ISG profile at baseline and following IFN challenge. Potential mechanisms may include augmented bystander apoptosis due to increased TRAIL expression (16-fold), in non-HESN cells. The study also identified two negative regulators of ISG induction associated with the HESN phenotype. Robust upregulation of SOCS-1 and IRF-1, in addition to HDM2, could contribute to the strict regulation of proinflammatory and proapoptotic ISGs in HESN cells. As reducing IRF-1 in the non-HESN cells resulted in the identified HESN ISG profile, and decreased HIV susceptibility, the unique HESN ISG profile could be a correlate of protection against HIV infection.

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