| Literature DB >> 32433762 |
Bruktawit A Goshu1,2, Hui Chen1,2, Maha Moussa1, Jie Cheng1, Marta Catalfamo1.
Abstract
In chronic HIV infection, virus-specific cytotoxic CD8 T cells showed expression of checkpoint receptors and impaired function. Therefore, restoration of CD8 T-cell function is critical in cure strategies. Here, we show that in vitro blockade of programmed cell death ligand 1 (PD-L1) by an anti-PD-L1 antibody (avelumab) in combination with recombinant human interleukin-15 (rhIL-15) synergistically enhanced cytokine secretion by proliferating HIVGag-specific CD8 T cells. In addition, these CD8 T cells have a CXCR3+PD1-/low phenotype, suggesting a potential to traffic into peripheral tissues. In vitro, proliferating CD8 T cells express PD-L1 suggesting that anti-PD-L1 treatment also targets virus-specific CD8 T cells. Together, these data indicate that rhIL-15/avelumab combination therapy could be a useful strategy to enhance CD8 T-cell function in cure strategies.Entities:
Keywords: HIV-specific CD8 T cells; PD-L1 blockade; rhIL-15
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Year: 2020 PMID: 32433762 PMCID: PMC7529035 DOI: 10.1093/infdis/jiaa269
Source DB: PubMed Journal: J Infect Dis ISSN: 0022-1899 Impact factor: 5.226