Human Macrophages Secrete Both Interferon α and Interferon β Proteins During Infection with <i>Mycobacterium tuberculosis</i>

Mycobacterium tuberculosis (Mtb) infection activates type I interferons (IFNs), which are crucial mediators of tuberculosis pathogenesis. Despite assumptions that IFNα and IFNβ are secreted by human macrophages, direct protein quantification in primary monocyte-derived macrophages (MDMs) is surprisingly lacking. Here, we demonstrate measurable IFNα and IFNβ secretion by MDMs infected with both virulent (H37Rv) and attenuated (H37Ra) Mtb strains as early as 48 h postinfection, with levels persisting at 120 h. These findings challenge existing assumptions about type I IFN kinetics and highlight the importance of timing in experimental designs and provide a foundation for exploring their role in host–pathogen interactions.

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Publication Details

Journal
Journal of Interferon & Cytokine Research
Published
2026-04-27
DOI
https://doi.org/10.1177/10799907261446997
Primary Topic
Tuberculosis Research and Epidemiology
Type
article
Field-Weighted Citation Impact
0.00
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article

Human Macrophages Secrete Both Interferon α and Interferon β Proteins During Infection with Mycobacterium tuberculosis

Gina Leisching, V Bondet, Anjali S Yennemadi, Sean Donohue et al.
Journal of Interferon & Cytokine Research
Tuberculosis Research and Epidemiology
article

Human Macrophages Secrete Both Interferon α and Interferon β Proteins During Infection with Mycobacterium tuberculosis

Gina Leisching, V Bondet, Anjali S Yennemadi, Sean Donohue, D Duffy, Joseph Keane, Donal Cox
article en

Abstract

Mycobacterium tuberculosis (Mtb) infection activates type I interferons (IFNs), which are crucial mediators of tuberculosis pathogenesis. Despite assumptions that IFNα and IFNβ are secreted by human macrophages, direct protein quantification in primary monocyte-derived macrophages (MDMs) is surprisingly lacking. Here, we demonstrate measurable IFNα and IFNβ secretion by MDMs infected with both virulent (H37Rv) and attenuated (H37Ra) Mtb strains as early as 48 h postinfection, with levels persisting at 120 h. These findings challenge existing assumptions about type I IFN kinetics and highlight the importance of timing in experimental designs and provide a foundation for exploring their role in host–pathogen interactions.

Journal of Interferon & Cytokine Research
Institut Pasteur (FR), Université Paris Cité (FR), Trinity College Dublin (IE), St. James's Hospital (IE)
Good health and well-being
Openalex Percentile: Top 10%
Tuberculosis Research and Epidemiology
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