Macrophage-T Cell Physical Interaction Modulates IFN-γ Secretion

Macrophages and T cells communicate under homeostatic and pathological conditions. Previous studies elucidated biochemical crosstalk between macrophages and T cells. However, recent technological advances in multiplex tissue imaging reveal that these cells are often located proximally. Notably, recent clinical studies link the proximity of macrophages and T cells to cancer outcomes. These observations suggest that physical contact between the two cell types might influence their phenotype and activity. However, systematic investigations of the potential role of physical contact between these cells are lacking. To address this gap, we developed three-dimensional (3D) coculture assays to study the potential role of physical contact between naïve macrophages and activated CD8<sup>+</sup> T cells cultured in 3D Matrigel matrix. Under contact conditions, macrophages and T cells were coencapsulated in the same matrix, whereas under no-contact conditions, they were cultured in matrix, separated by a Transwell membrane. Our findings indicated that T cells changed their migration behavior by stopping and moving over the surface of naïve macrophages during coculture. We quantitatively determined T cells establish durable contact with macrophages, which informed our hypothesis that physical interactions between macrophage-T cells may induce phenotypic changes. Physical contact led to a 3-fold increase in IFN-γ secretion, a key effector molecule of CD8<sup>+</sup> T cells. The increase in IFN-γ was mediated by JAK and led to a 2-fold upregulation of ICAM-1 and increased PD-L1 expression. Our findings point to a model whereby activated T cells migrate toward macrophages and are held in proximity by ICAM-1 adhesion molecules, leading to increased production of IFN-γ and PD-L1 expression. These results establish that physical contact is an important determinant of macrophage and T cell states. Broadly, our study establishes a foundation to use biomaterials as a tool to provide mechanistic insights into heterotypic cell interactions to enable rational manipulation of the immune response.

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Publication Details

Journal
ACS Applied Materials & Interfaces
Published
2025-09-01
DOI
https://doi.org/10.1021/acsami.5c05333
Primary Topic
T-cell and B-cell Immunology
Type
article
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article

Macrophage-T Cell Physical Interaction Modulates IFN-γ Secretion

Zerin Mahzabin Khan, Daniel Michaud, Michael Griffith Bibbey, Suyog Shaha et al.
ACS Applied Materials & Interfaces
T-cell and B-cell Immunology
article

Macrophage-T Cell Physical Interaction Modulates IFN-γ Secretion

Zerin Mahzabin Khan, Daniel Michaud, Michael Griffith Bibbey, Suyog Shaha, Kolade Adebowale, Samir Mitragotri, Jennifer L. Guerriero
article en

Abstract

Macrophages and T cells communicate under homeostatic and pathological conditions. Previous studies elucidated biochemical crosstalk between macrophages and T cells. However, recent technological advances in multiplex tissue imaging reveal that these cells are often located proximally. Notably, recent clinical studies link the proximity of macrophages and T cells to cancer outcomes. These observations suggest that physical contact between the two cell types might influence their phenotype and activity. However, systematic investigations of the potential role of physical contact between these cells are lacking. To address this gap, we developed three-dimensional (3D) coculture assays to study the potential role of physical contact between naïve macrophages and activated CD8<sup>+</sup> T cells cultured in 3D Matrigel matrix. Under contact conditions, macrophages and T cells were coencapsulated in the same matrix, whereas under no-contact conditions, they were cultured in matrix, separated by a Transwell membrane. Our findings indicated that T cells changed their migration behavior by stopping and moving over the surface of naïve macrophages during coculture. We quantitatively determined T cells establish durable contact with macrophages, which informed our hypothesis that physical interactions between macrophage-T cells may induce phenotypic changes. Physical contact led to a 3-fold increase in IFN-γ secretion, a key effector molecule of CD8<sup>+</sup> T cells. The increase in IFN-γ was mediated by JAK and led to a 2-fold upregulation of ICAM-1 and increased PD-L1 expression. Our findings point to a model whereby activated T cells migrate toward macrophages and are held in proximity by ICAM-1 adhesion molecules, leading to increased production of IFN-γ and PD-L1 expression. These results establish that physical contact is an important determinant of macrophage and T cell states. Broadly, our study establishes a foundation to use biomaterials as a tool to provide mechanistic insights into heterotypic cell interactions to enable rational manipulation of the immune response.

ACS Applied Materials & InterfacesVol. 17(36)
Brigham and Women's Hospital (US), Harvard University (US), Harvard University Press (US), Breast Cancer Care (GB), Dana-Farber Cancer Institute (US), Breast Center (CH), Inspire (CH), La Jolla Bioengineering Institute (US), Center for Cancer Research (US), Dana-Farber Brigham Cancer Center (US)
Openalex Percentile: Top 75%
T-cell and B-cell Immunology
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