# The power of GM-CSF: immune regulation in the defense against Phialophora verrucosa infection

## TL;DR

This study shows that GM-CSF is crucial for fighting Phialophora verrucosa infections by boosting immune responses and fungal clearance.

## Contribution

The study demonstrates that GM-CSF is essential for effective antifungal immunity against dematiaceous fungi.

## Key findings

- GM-CSF deficiency delays fungal clearance and worsens disease progression in mice.
- GM-CSF enhances macrophage chemotaxis and neutrophil phagocytosis in vitro.
- IFN-γ increase in GM-CSF-deficient mice cannot compensate for immune defects.

## Abstract

Phialophora verrucosa, a dematiaceous fungus, causes serious infections such as phaeohyphomycosis. These infections can severely impair patient quality of life and may be life-threatening. Current understanding of host immune defenses against this pathogen remains limited.

This study aims to investigate the role of granulocyte-macrophage colony-stimulating factor (GM-CSF) in host defense against P. verrucosa. Using both in vivo and in vitro models, the current study specifically examines how GM-CSF deficiency impacts immune responses and fungal clearance.

C57BL/6 wild-type (WT) and GM-CSF-deficient (Csf2 KO) mice were infected subcutaneously in the footpad with live P. verrucosa conidia. Skin lesion appearance and foot swelling were monitored for 4 weeks. At specific time points, footpad tissues were collected for PAS, CD68, and MPO staining, and colony-forming units were calculated to assess fungal load. Serum and tissue homogenates were analyzed for cytokine levels. Bone marrow-derived macrophages and neutrophils were isolated to evaluate GM-CSF’ s impact on chemotaxis, phagocytosis, and killing functions.

Compared to WT mice, GM-CSF deficiency significantly delayed fungal clearance and prolonged disease progression, accompanied by reduced inflammatory responses and decreased neutrophil infiltration. In vitro, GM-CSF supplementation restored macrophage chemotaxis and enhanced neutrophil phagocytic activity, but did not affect their killing efficiency. A compensatory increase in IFN-γ levels in Csf2 KO mice was insufficient to overcome the immune defects caused by GM-CSF deficiency.

This study reveals the indispensable role of GM-CSF in antifungal immunity and its potential as a therapeutic target for controlling infections caused by dematiaceous fungi.