CD4+ T cells re-wire granuloma cellularity and regulatory networks to promote immunomodulation following Mtb reinfection

Immunological priming-in the context of either prior infection or vaccination-elicits protective responses against subsequent Mycobacterium tuberculosis (Mtb) infection. However, the changes that occur in the lung cellular milieu post-primary Mtb infection and their contributions to protection upon reinfection remain poorly understood. Using clinical and microbiological endpoints in a non-human primate reinfection model, we demonstrated that prior Mtb infection elicited a long-lasting protective response against subsequent Mtb exposure and was CD4<sup>+</sup> T cell dependent. By analyzing data from primary infection, reinfection, and reinfection-CD4<sup>+</sup> T cell-depleted granulomas, we found that the presence of CD4<sup>+</sup> T cells during reinfection resulted in a less inflammatory lung milieu characterized by reprogrammed CD8<sup>+</sup> T cells, reduced neutrophilia, and blunted type 1 immune signaling among myeloid cells. These results open avenues for developing vaccines and therapeutics that not only target lymphocytes but also modulate innate immune cells to limit tuberculosis (TB) disease.

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Publication Details

Journal
Immunity
Published
2024-08-29
DOI
https://doi.org/10.1016/j.immuni.2024.08.002
Citations
36
Primary Topic
Tuberculosis Research and Epidemiology
Type
article
Field-Weighted Citation Impact
14.00

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article

CD4+ T cells re-wire granuloma cellularity and regulatory networks to promote immunomodulation following Mtb reinfection

Charles A. Scanga, Michael C. Chao, H. Jacob Borish, Son Nguyen et al.
36 citations
Immunity
Tuberculosis Research and Epidemiology
14.00
article

CD4+ T cells re-wire granuloma cellularity and regulatory networks to promote immunomodulation following Mtb reinfection

Charles A. Scanga, Michael C. Chao, H. Jacob Borish, Son Nguyen, Philana Ling Lin, Mark Rodgers, Edwin Klein, Qikun Wang, Sarah K. Nyquist, Jaime Tomko, Bonnie Berger, Joshua D. Bromley, Pauline A Maiello, Hannah P. Gideon, Jacob M. Rosenberg, Sharie Keanne C. Ganchua, Douaa Mugahid, JoAnne L. Flynn, Alex K. Shalek, Sarah M. Fortune, Kara Kracinovsky, Roisin Floyd-O’Sullivan
article en
36 citations

Abstract

Immunological priming-in the context of either prior infection or vaccination-elicits protective responses against subsequent Mycobacterium tuberculosis (Mtb) infection. However, the changes that occur in the lung cellular milieu post-primary Mtb infection and their contributions to protection upon reinfection remain poorly understood. Using clinical and microbiological endpoints in a non-human primate reinfection model, we demonstrated that prior Mtb infection elicited a long-lasting protective response against subsequent Mtb exposure and was CD4<sup>+</sup> T cell dependent. By analyzing data from primary infection, reinfection, and reinfection-CD4<sup>+</sup> T cell-depleted granulomas, we found that the presence of CD4<sup>+</sup> T cells during reinfection resulted in a less inflammatory lung milieu characterized by reprogrammed CD8<sup>+</sup> T cells, reduced neutrophilia, and blunted type 1 immune signaling among myeloid cells. These results open avenues for developing vaccines and therapeutics that not only target lymphocytes but also modulate innate immune cells to limit tuberculosis (TB) disease.

ImmunityVol. 57(10)
Broad Institute (US), University of Pittsburgh (US), Ragon Institute of MGH, MIT and Harvard (US), Children's Hospital of Pittsburgh (US), Massachusetts Institute of Technology (US)
Bill and Melinda Gates Foundation, Harvard University, Harvard University Center for AIDS Research, Harvard Catalyst, University of Pittsburgh, National Institutes of Health, Center for AIDS Research, University of Washington, National Institute of Allergy and Infectious Diseases, Office of Research Infrastructure Programs, National Institutes of Health
Zero hunger
Openalex Percentile: Top 1%
Tuberculosis Research and Epidemiology
14.00
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