Interferon-γ Stimulation Fails to Restrict <i>Mycobacterium tuberculosis</i> Growth in Human Monocyte-Derived and Alveolar Macrophages

We examined whether interferon-γ (IFNG) restricts Mycobacterium tuberculosis growth in human macrophages across a range of conditions and methods. We observed an IFNG-dependent enhancement of bacterial replication in macrophage colony-stimulating factor-differentiated monocyte-derived macrophages (4.84 × 105 colony-forming units [CFU] IFNG stimulated vs 2.48 × 105 CFU untreated, P < .001) with 4 M. tuberculosis strains. M. tuberculosis replication was not restricted by IFNG treatment of alveolar macrophages. In agreement with previous studies, IFNG-stimulated murine bone marrow-derived macrophages effectively restricted M. tuberculosis replication. These data suggest that M. tuberculosis resists IFNG-stimulated immunity within human macrophages with implications for distinct host species immune responses.

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Publication Details

Journal
The Journal of Infectious Diseases
Published
2025-04-26
DOI
https://doi.org/10.1093/infdis/jiaf220
Citations
2
Primary Topic
Tuberculosis Research and Epidemiology
Type
article
Field-Weighted Citation Impact
2.79
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article

Interferon-γ Stimulation Fails to Restrict Mycobacterium tuberculosis Growth in Human Monocyte-Derived and Alveolar Macrophages

Shawn Skerrett, Mark C. Fernandez, Thomas R. Hawn, Glenna J. Peterson et al.
2 citations
The Journal of Infectious Diseases
Tuberculosis Research and Epidemiology
2.79
article

Interferon-γ Stimulation Fails to Restrict Mycobacterium tuberculosis Growth in Human Monocyte-Derived and Alveolar Macrophages

Shawn Skerrett, Mark C. Fernandez, Thomas R. Hawn, Glenna J. Peterson, Chinh T. Lé
article en
2 citations

Abstract

We examined whether interferon-γ (IFNG) restricts Mycobacterium tuberculosis growth in human macrophages across a range of conditions and methods. We observed an IFNG-dependent enhancement of bacterial replication in macrophage colony-stimulating factor-differentiated monocyte-derived macrophages (4.84 × 105 colony-forming units [CFU] IFNG stimulated vs 2.48 × 105 CFU untreated, P < .001) with 4 M. tuberculosis strains. M. tuberculosis replication was not restricted by IFNG treatment of alveolar macrophages. In agreement with previous studies, IFNG-stimulated murine bone marrow-derived macrophages effectively restricted M. tuberculosis replication. These data suggest that M. tuberculosis resists IFNG-stimulated immunity within human macrophages with implications for distinct host species immune responses.

The Journal of Infectious DiseasesVol. 232(3)
University of Washington (US)
Openalex Percentile: Top 11%
Tuberculosis Research and Epidemiology
2.79
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