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T follicular regulatory cells in food allergy promote IgE via IL-4
Qiang Chen, Abdullahi M. Abdi, Wei Luo, Xue Yuan, Alexander L. Dent
Qiang Chen, Abdullahi M. Abdi, Wei Luo, Xue Yuan, Alexander L. Dent
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Research Article Immunology

T follicular regulatory cells in food allergy promote IgE via IL-4

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Abstract

T follicular regulatory (TFR) cells are found in the germinal center (GC) response and, along with T follicular helper (TFH) cells, help to control the development of high-affinity antibodies (Ab). Although TFR cells are generally thought to repress GC B cells and the Ab response, we have previously shown that in a mouse food allergy model, TFR cells produce IL-10 and play an essential helper role such that in the absence of TFR cells, IgE responses are diminished. Here we show that in this food allergy response, TFR cells produced IL-4 that promotes the generation of antigen-specific IgE. We show that food allergy–primed TFR cells specifically upregulate IL-4 gene transcription and produce functional IL-4 that promoted IgE responses both in vitro and in vivo. We determined that IgE responses are dependent on a high level of IL-4 produced by follicular T cells in the GC, explaining the need for IL-4 produced by TFR cells in the food allergy response. Overall, our findings have demonstrated that in food allergy, TFR cells can produce IL-4 and regulate IgE in a manner that augments the role of TFH cells in IgE responses.

Authors

Qiang Chen, Abdullahi M. Abdi, Wei Luo, Xue Yuan, Alexander L. Dent

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Figure 2

Gene profiling of naive TFR cells and TFR cells in food allergy.

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Gene profiling of naive TFR cells and TFR cells in food allergy.
(A–C) H...
(A–C) Heatmap of selected genes in TFR cells. TFR cells were sorted from the mLNs plus spleen of naive mice and mice at day 12 after PCT sensitization at day 1 and day 8. Total RNA was extracted and subjected to bulk RNA-Seq and analysis. Genes associated with TFH cells (A), Th2 cells (B), and Il4 gene regulation (C) were compared between naive mice and PCT-sensitized mice. The heatmap represents the values of log2FPKM. Significance was defined by |log2FC| > 1 and adjusted P < 0.05. (D) mRNA expression of selected genes in TFR cells by qPCR. TFR cells were sorted from naive and PCT-sensitized mice. RNA was extracted, and the first-strand cDNA was synthesized. Levels of mRNA for selected genes was measured using qPCR. n = 4. *P < 0.05, **P < 0.01 by t test (D). Data were from 1 independent experiment. Heatmaps were created using pheatmap package with clustering rows in R (4.3.1).

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