HIV-1 reservoirs in urethral macrophages of patients under suppressive antiretroviral therapy.
Yonatan GanorFernando RealAlexis SennepinCharles-Antoine DutertreLisa PrevedelLin XuDaniela TudorBénédicte CharmeteauAnne Couedel-CourteilleSabrina MarionAli-Redha ZenakJean-Pierre JourdainZhicheng ZhouAlain SchmittClaude CapronEliseo A EugeninRémi CheynierMarc RevolSarra CristofariAnne HosmalinMorgane BomselPublished in: Nature microbiology (2019)
Human immunodeficiency virus type 1 (HIV-1) eradication is prevented by the establishment on infection of cellular HIV-1 reservoirs that are not fully characterized, especially in genital mucosal tissues (the main HIV-1 entry portal on sexual transmission). Here, we show, using penile tissues from HIV-1-infected individuals under suppressive combination antiretroviral therapy, that urethral macrophages contain integrated HIV-1 DNA, RNA, proteins and intact virions in virus-containing compartment-like structures, whereas viral components remain undetectable in urethral T cells. Moreover, urethral cells specifically release replication-competent infectious HIV-1 following reactivation with the macrophage activator lipopolysaccharide, while the T-cell activator phytohaemagglutinin is ineffective. HIV-1 urethral reservoirs localize preferentially in a subset of polarized macrophages that highly expresses the interleukin-1 receptor, CD206 and interleukin-4 receptor, but not CD163. To our knowledge, these results are the first evidence that human urethral tissue macrophages constitute a principal HIV-1 reservoir. Such findings are determinant for therapeutic strategies aimed at HIV-1 eradication.
Keyphrases
- antiretroviral therapy
- hiv infected
- human immunodeficiency virus
- hiv positive
- hiv aids
- hiv infected patients
- hepatitis c virus
- hiv testing
- men who have sex with men
- endothelial cells
- sars cov
- gene expression
- inflammatory response
- binding protein
- toll like receptor
- cell proliferation
- signaling pathway
- cell free
- ejection fraction
- nuclear factor
- mass spectrometry
- patient reported outcomes
- induced apoptosis
- lps induced
- cell cycle arrest
- helicobacter pylori infection