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Dectin-1 stimulation promotes a distinct inflammatory signature in the setting of HIV-infection and aging.

Aging | 2023

Dectin-1 is an innate immune receptor that recognizes and binds β-1, 3/1, 6 glucans on fungi. We evaluated Dectin-1 function in myeloid cells in a cohort of HIV-positive and HIV-negative young and older adults. Stimulation of monocytes with β-D-glucans induced a pro-inflammatory phenotype in monocytes of HIV-infected individuals that was characterized by increased levels of IL-12, TNF-α, and IL-6, with some age-associated cytokine increases also noted. Dendritic cells showed a striking HIV-associated increase in IFN-α production. These increases in cytokine production paralleled increases in Dectin-1 surface expression in both monocytes and dendritic cells that were noted with both HIV and aging. Differential gene expression analysis showed that HIV-positive older adults had a distinct gene signature compared to other cohorts characterized by a robust TNF-α and coagulation response (increased at baseline), a persistent IFN-α and IFN-γ response, and an activated dendritic cell signature/M1 macrophage signature upon Dectin-1 stimulation. Dectin-1 stimulation induced a strong upregulation of MTORC1 signaling in all cohorts, although increased in the HIV-Older cohort (stimulation and baseline). Overall, our study demonstrates that the HIV Aging population has a distinct immune signature in response to Dectin-1 stimulation. This signature may contribute to the pro-inflammatory environment that is associated with HIV and aging.

Pubmed ID: 37606991 RIS Download

Associated grants

  • Agency: NIA NIH HHS, United States
    Id: K76 AG064548
  • Agency: NIA NIH HHS, United States
    Id: R24 AG044325
  • Agency: NIA NIH HHS, United States
    Id: R01 AG055362
  • Agency: NIA NIH HHS, United States
    Id: P30 AG021342
  • Agency: NIA NIH HHS, United States
    Id: R03 AG050947
  • Agency: NIA NIH HHS, United States
    Id: K24 AG042489
  • Agency: Howard Hughes Medical Institute, United States

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