Alternatively activated monocyte-derived myeloid cells promote extracellular pathogen persistence within pulmonary

Yufan Zheng1, Makheni Jean Pierre1,2, Eduard Ansaldo1

  • 1Molecular Mycology and Immunity Section, Laboratory of Host Immunity and Microbiome, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, 20892, USA.

Insights

Latent fungal infections persist because CD4+ T helper 2 cells promote myeloid cell activity that hinders fungal clearance. Targeting this T cell-myeloid circuit may treat persistent fungal infections.

Area of Science:

  • Immunology
  • Mycology
  • Infectious Diseases

Background:

  • Inhaled fungal pathogens establish latent infections within granulomas, with potential for reactivation into invasive disease.
  • Mechanisms preventing sterilizing immunity against latent fungal infections are not well understood.

Purpose of the Study:

  • To investigate the immune dynamics and cellular architecture of cryptococcal granulomas during latent infection.
  • To elucidate the role of T helper cells and myeloid cells in controlling or promoting fungal persistence.

Main Methods:

  • Spatial transcriptomics and flow cytometry were employed to analyze granuloma composition.
  • Fate mapping and murine genetic models were utilized to track immune cell function and interactions.
  • Fungal localization within granulomas was assessed.

Main Results:

  • Alternative activation of monocyte-derived myeloid cells by CD4+ T helper 2 cells was found to impede pulmonary fungal clearance.
  • Contrary to previous beliefs, alternatively activated myeloid cells do not serve as a primary replication niche for the fungus.
  • Cryptococcus was predominantly observed in the extracellular environment within granulomas.

Conclusions:

  • A T helper 2 cell-myeloid cell circuit creates a local immunosuppressive environment, promoting extracellular fungal persistence.
  • This circuit represents a potential therapeutic target for host-directed strategies against latent fungal infections.

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