Abstract

HemoHIM, an herbal preparation of three edible herbs (Angelica gigas Nakai, Cnidium officinale Makino, Paeonia japonica Miyabe) is known to increase the Th1 immune response as well as reduce the allergic response in human mast cells. Here, our goal was to determine whether or not HemoHIM could induce Th1 cell differentiation as well as inhibit the development of airway inflammation. To study Th1/Th2 cell differentiation, naive CD4+ T cells isolated from C57BL/6 mouse spleens were cultured with or without HemoHIM. To examine airway inflammation, C57BL/6 mice were fed HemoHIM for 4 weeks before sensitization and provocation with ovalbumin (OVA). In an in vitro experiment, naive CD4+ T cells displayed increased Th1 (IFN-γ+ cell) as well as decreased Th2 (IL-4+ cell) differentiation in a HemoHIM concentration-dependent manner. Furthermore, in an airway inflammation mice model, eosinophil numbers in BALF, serum levels of OVA-specific IgE and IgG1, and cytokine (IL-4, IL-5, and IL-13) levels in BALF and the supernatant of splenocytes all decreased upon HemoHIM (100 mg/kg body weight) pretreatment (4 weeks). These results show that HemoHIM attenuated allergic airway inflammation in the mouse model through regulation of the Th1/Th2 balance.

Highlights

  • Airway inflammation is an important symptom of asthma

  • Eotaxin, RANTES, IL-4, IL-5, and IL-13, which are produced by Th2 cells, are all related to airway hyperresponsiveness as well as inflammatory changes through activation of eosinophils and immunoglobulin E (IgE) production by B cells [12,13,14]

  • The aim of this study was to investigate the effects of HemoHIM on the prevention of airway inflammation

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Summary

Introduction

Airway inflammation is an important symptom of asthma. Bronchial asthma is characterized by airway hyperresponsiveness, eosinophilic airway inflammation, and increased immunoglobulin E (IgE) levels [9,10,11]. Eotaxin, RANTES, IL-4, IL-5, and IL-13, which are produced by Th2 cells, are all related to airway hyperresponsiveness as well as inflammatory changes through activation of eosinophils and IgE production by B cells [12,13,14]. Since the influx and differentiation of Th2 cells are important factors in the development and aggravation of asthma, recent studies have targeted the activation of Th2 cells or regulation of the Th1/2 balance to prevent and treat asthma [15,16,17]

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