» Articles » PMID: 30737355

Diet Modulates Colonic T Cell Responses by Regulating the Expression of a Antigen

Overview
Journal Sci Immunol
Date 2019 Feb 10
PMID 30737355
Citations 44
Authors
Affiliations
Soon will be listed here.
Abstract

T cell responses to symbionts in the intestine drive tolerance or inflammation depending on the genetic background of the host. These symbionts in the gut sense the available nutrients and adapt their metabolic programs to use these nutrients efficiently. Here, we ask whether diet can alter the expression of a bacterial antigen to modulate adaptive immune responses. We generated a CD4 T cell hybridoma, BθOM, specific for (). Adoptively transferred transgenic T cells expressing the BθOM TCR proliferated in the colon, colon-draining lymph node, and spleen in colonized healthy mice and differentiated into regulatory T cells (T) and effector T cells (T). Depletion of -specific T resulted in colitis, showing that a single protein expressed by can drive differentiation of T that self-regulate T to prevent disease. We found that BθOM T cells recognized a peptide derived from a single protein, BT4295, whose expression is regulated by nutrients, with glucose being a strong catabolite repressor. Mice fed a high-glucose diet had a greatly reduced activation of BθOM T cells in the colon. These studies establish that the immune response to specific bacterial antigens can be modified by changes in the diet by altering antigen expression in the microbe.

Citing Articles

coordinates the IL-10 inducing activity of .

Engelhart M, Brock O, Till J, Glowacki R, Cantwell J, Clarke D Microbiol Spectr. 2025; 13(3):e0166924.

PMID: 39868786 PMC: 11878027. DOI: 10.1128/spectrum.01669-24.


Engineered Bacteria for Disease Diagnosis and Treatment Using Synthetic Biology.

Jin K, Huang Y, Che H, Wu Y Microb Biotechnol. 2025; 18(1):e70080.

PMID: 39801378 PMC: 11725985. DOI: 10.1111/1751-7915.70080.


Discovery and engineering of the antibody response to a prominent skin commensal.

Bousbaine D, Bauman K, Chen Y, Lalgudi P, Nguyen T, Swenson J Nature. 2024; 638(8052):1054-1064.

PMID: 39662508 DOI: 10.1038/s41586-024-08489-4.


Hierarchical glycolytic pathways control the carbohydrate utilization regulator in human gut .

Kabonick S, Verma K, Modesto J, Pearce V, Winokur K, Groisman E bioRxiv. 2024; .

PMID: 39605394 PMC: 11601483. DOI: 10.1101/2024.11.13.623061.


The Role of the Gut Microbiome in Inflammatory Bowel Disease: The Middle East Perspective.

El-Sayed A, Kapila D, Taha R, El-Sayed S, Mahen M, Taha R J Pers Med. 2024; 14(6).

PMID: 38929872 PMC: 11204866. DOI: 10.3390/jpm14060652.


References
1.
Koropatkin N, Cameron E, Martens E . How glycan metabolism shapes the human gut microbiota. Nat Rev Microbiol. 2012; 10(5):323-35. PMC: 4005082. DOI: 10.1038/nrmicro2746. View

2.
Hand T, Dos Santos L, Bouladoux N, Molloy M, Pagan A, Pepper M . Acute gastrointestinal infection induces long-lived microbiota-specific T cell responses. Science. 2012; 337(6101):1553-6. PMC: 3784339. DOI: 10.1126/science.1220961. View

3.
Cong Y, Feng T, Fujihashi K, Schoeb T, Elson C . A dominant, coordinated T regulatory cell-IgA response to the intestinal microbiota. Proc Natl Acad Sci U S A. 2009; 106(46):19256-61. PMC: 2780781. DOI: 10.1073/pnas.0812681106. View

4.
Hickey C, Kuhn K, Donermeyer D, Porter N, Jin C, Cameron E . Colitogenic Bacteroides thetaiotaomicron Antigens Access Host Immune Cells in a Sulfatase-Dependent Manner via Outer Membrane Vesicles. Cell Host Microbe. 2015; 17(5):672-80. PMC: 4432250. DOI: 10.1016/j.chom.2015.04.002. View

5.
Chai J, Peng Y, Rengarajan S, Solomon B, Ai T, Shen Z . species are potent drivers of colonic T cell responses in homeostasis and inflammation. Sci Immunol. 2017; 2(13). PMC: 5684094. DOI: 10.1126/sciimmunol.aal5068. View