Abstract

The dysfunction of regulatory B cells (Breg) may result in immune inflammation such as allergic rhinitis (AR); the underlying mechanism is not fully understood yet. Short-chain fatty acids, such as propionic acid (PA), have immune regulatory functions. This study is aimed at testing a hypothesis that modulates PA production alleviating airway allergy through maintaining Breg functions. B cells were isolated from the blood obtained from AR patients and healthy control (HC) subjects. The stabilization of IL-10 mRNA in B cells was tested with RT-qPCR. An AR mouse model was developed to test the role of PA in stabilizing the IL-10 expression in B cells. We found that the serum PA levels were negatively correlated with the serum Th2 cytokine levels in AR patients. Serum PA levels were positively associated with peripheral CD5+ B cell frequency in AR patients; the CD5+ B cells were also IL-10+. The spontaneous IL-10 mRNA decay was observed in B cells, which was prevented by the presence of PA through activating GPR43. PA counteracted the effects of Tristetraprolin (TTP) on inducing IL-10 mRNA decay in B cells through the AKT/T-bet/granzyme B pathway. Administration of Yupinfeng San, a Chinese traditional medical formula, or indole-3-PA, induced PA production by intestinal bacteria to stabilize the IL-10 expression in B cells, which promoted the allergen specific immunotherapy, and efficiently alleviated experimental AR. In summary, the data show that CD5+ B cells produce IL-10. The serum lower PA levels are associated with the lower frequency of CD5+ B cells in AR patients. Administration with Yupinfeng San or indole-3-PA can improve Breg functions and alleviate experimental AR.

Highlights

  • The immune regulation indicates a balance between activation and suppression of effector immune cells to achieve an efficient immune response without causing damage in the host that is carried out by a group of immune cells

  • We found that the serum levels of acetic acids (AA), butyric acids (BA), and propionic acids (PA) were lower in the allergic rhinitis (AR) group than in the healthy control (HC) group (Figures 1(a)–1(c))

  • We found that the serum PA levels were lower in AR patients, which were negatively correlated with the Th2 cytokine levels in the serum

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Summary

Introduction

The immune regulation indicates a balance between activation and suppression of effector immune cells to achieve an efficient immune response without causing damage in the host that is carried out by a group of immune cells. This group of cells is designated immune regulatory cells, such as, but not limited to, regulatory T cells (Treg) and regulatory B cells (Breg) [1, 2]. Maintaining immune regulatory cells at the optimal functional status may help to generate new therapies for immune diseases. Several cell markers have been described for Bregs, such as CD5, CD34, CD73, CD71, or CD25, indicating that Breg markers and functions may be modified by relevant

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