Early and opposing neutrophil and CD4 T cell responses shape pulmonary tuberculosis pathology

Pulmonary Mycobacterium tuberculosis (Mtb) infection results in a variety of heterogeneous lesion structures, from necrotic granulomas to alveolitis, but the mechanisms regulating their development remain unclear. Using a mouse model of concomitant immunity and subsequent aerosol infection, we demonstrate that counter regulation between neutrophils and CD4 T cells occurs very early during infection and governs these distinct pathologies. In primary Mtb infection, a dysregulated feed-forward circuit of neutrophil recruitment occurs, in which neutrophils hinder CD4 T cell interactions with infected macrophages, cause granuloma necrosis, and establish a replicative niche that drives a two-log increase in lung bacterial burden. Conversely, the rapid recruitment and activation of T cells due to concomitant immunity promotes local macrophage activation and dampens detrimental neutrophil responses. Together, these studies uncover fundamental determinants of tuberculosis lung pathology, which have important implications for new strategies to prevent or treat tuberculosis.

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Publication Details

Journal
The Journal of Experimental Medicine
Published
2025-06-28
DOI
https://doi.org/10.1084/jem.20250161
Citations
11
Primary Topic
Tuberculosis Research and Epidemiology
Type
article
Field-Weighted Citation Impact
15.36

Funders

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article

Early and opposing neutrophil and CD4 T cell responses shape pulmonary tuberculosis pathology

John D. Aitchison, Fergal J. Duffy, Maxwell L. Neal, Michael Gale et al.
11 citations
The Journal of Experimental Medicine
Tuberculosis Research and Epidemiology
15.36
article

Early and opposing neutrophil and CD4 T cell responses shape pulmonary tuberculosis pathology

John D. Aitchison, Fergal J. Duffy, Maxwell L. Neal, Michael Gale, Sylvia M. Stull, Jasmine Wilson, Kimberly A. Foster, Courtney R. Plumlee, Andrew T. Gustin, Alan Aderem, Alan H. Diercks, Benjamin H. Gern, Kevin B. Urdahl, Michael Y. Gerner, Mehnaz Halima, Josepha Klas, S. B. Cohen, Molly E. Kanagy
article en
11 citations

Abstract

Pulmonary Mycobacterium tuberculosis (Mtb) infection results in a variety of heterogeneous lesion structures, from necrotic granulomas to alveolitis, but the mechanisms regulating their development remain unclear. Using a mouse model of concomitant immunity and subsequent aerosol infection, we demonstrate that counter regulation between neutrophils and CD4 T cells occurs very early during infection and governs these distinct pathologies. In primary Mtb infection, a dysregulated feed-forward circuit of neutrophil recruitment occurs, in which neutrophils hinder CD4 T cell interactions with infected macrophages, cause granuloma necrosis, and establish a replicative niche that drives a two-log increase in lung bacterial burden. Conversely, the rapid recruitment and activation of T cells due to concomitant immunity promotes local macrophage activation and dampens detrimental neutrophil responses. Together, these studies uncover fundamental determinants of tuberculosis lung pathology, which have important implications for new strategies to prevent or treat tuberculosis.

The Journal of Experimental MedicineVol. 222(10)
Center for Infectious Disease Research (US), Infectious Disease Research Institute (US), University of Washington (US)
National Institutes of Health
Good health and well-being
Openalex Percentile: Top 1%
Tuberculosis Research and Epidemiology
15.36
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