Identification of antigen-presenting cell–T cell interactions driving immune responses to food

The intestinal immune system must concomitantly tolerate food and commensals and protect against pathogens. Antigen-presenting cells (APCs) orchestrate these immune responses by presenting luminal antigens to CD4<sup>+</sup> T cells and inducing their differentiation into regulatory (peripheral regulatory T cell) or inflammatory [T helper (Th) cell] subsets. We used a proximity labeling method (LIPSTIC) to identify APCs that presented dietary antigens under tolerizing and inflammatory conditions and to understand cellular mechanisms by which tolerance to food is induced and can be disrupted by infection. Helminth infections disrupted tolerance induction proportionally to the reduction in the ratio between tolerogenic APCs-including migratory dendritic cells (cDC1s) and Rorγt<sup>+</sup> APCs-and inflammatory APCs, which were primarily cDC2s. These inflammatory cDC2s expanded by helminth infection did not present dietary antigens, thus avoiding diet-specific Th2 responses.

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Publication Details

Journal
Science
Published
2024-12-19
DOI
https://doi.org/10.1126/science.ado5088
Citations
55
Primary Topic
Immune Cell Function and Interaction
Type
article
Field-Weighted Citation Impact
13.23
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article

Identification of antigen-presenting cell–T cell interactions driving immune responses to food

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55 citations
Science
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article

Identification of antigen-presenting cell–T cell interactions driving immune responses to food

Daria Esterházy, Mengze Lyu, Tiantian Liu, Maria Cecília Campos Canesso, Ainsley Lockhart, Gabriel D. Victora, Gregory F. Sonnenberg, Tiago B. R. Castro, Kenneth M. Murphy, Roham Parsa, Sandra Nakandakari-Higa, Juliana Bortolatto, Bernardo Sgarbi Reis, Julia B. W. Luehr, Daniel Mucida
article en
55 citations

Abstract

The intestinal immune system must concomitantly tolerate food and commensals and protect against pathogens. Antigen-presenting cells (APCs) orchestrate these immune responses by presenting luminal antigens to CD4<sup>+</sup> T cells and inducing their differentiation into regulatory (peripheral regulatory T cell) or inflammatory [T helper (Th) cell] subsets. We used a proximity labeling method (LIPSTIC) to identify APCs that presented dietary antigens under tolerizing and inflammatory conditions and to understand cellular mechanisms by which tolerance to food is induced and can be disrupted by infection. Helminth infections disrupted tolerance induction proportionally to the reduction in the ratio between tolerogenic APCs-including migratory dendritic cells (cDC1s) and Rorγt<sup>+</sup> APCs-and inflammatory APCs, which were primarily cDC2s. These inflammatory cDC2s expanded by helminth infection did not present dietary antigens, thus avoiding diet-specific Th2 responses.

ScienceVol. 387(6739)
Howard Hughes Medical Institute (US), Washington University in St. Louis (US), Cornell University (US), University of Chicago (US), Rockefeller University (US)
Zero hunger
Openalex Percentile: Top 1%
Immune Cell Function and Interaction
13.23
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