Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2015 Mar 15;8(3):4158-63.
eCollection 2015.

FOXP3(+)Treg/Th17 cell imbalance in lung tissues of mice with asthma

Affiliations

FOXP3(+)Treg/Th17 cell imbalance in lung tissues of mice with asthma

Hua Jiang et al. Int J Clin Exp Med. .

Abstract

Immunocyte imbalances, particularly of Th1 and Th2 type helper T (Th) cells, have been implicated in the pathogenesis of chronic inflammatory diseases like asthma. Recent studies have suggested an important role for the balance between Th17 cells and FOXP3(+) regulatory T cells (Treg). However, whether this balance is important in asthma remains unknown. This study sought to detect the populations of T cell subtypes (Th1, Th2, FOXP3(+) Treg, Th17) in lung tissue of a mouse model of asthma to understand the significance of immunocyte balances in the disease. An asthma model was generated by sensitizing ten pathogen-free BALB/c mice using a standard ovalbumin challenge; ten other mice were challenged with PBS to serve as a control group. Total white cells and differential cell counts were determined in bronchoalveolar lavage fluid, and percentages of T cell subtypes were determined using flow cytometry. The severity of inflammation in lung tissue was evaluated in tissue sections, and airway hyperresponsiveness was assessed by unrestrained plethysmography. In mice with asthma, compared to those in the control group, total white cell, eosinophil, monocyte, and lymphocyte cell counts were higher, and lung inflammation and airway hyperresponsiveness were more severe (P<0.05), indicating that the model of asthma was successfully generated. Further, mice with asthma had higher percentages of Th2 and Th17 cells and lower percentages of Th1 and Foxp3(+) Treg cells in lung tissue (P<0.05). Consequently, the ratios of Th1/Th2 cells and FOXP3(+)Treg/Th17 cells were higher in the asthma group (P<0.05). Thus, in addition to the imbalance of Th1/Th2 cells, an imbalance of FOXP3(+)Treg/Th17 cells may play an important role in the pathogenesis of asthma.

Keywords: Asthma; FOXP3+Treg cell; Th17; ovalbumin.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Inflammatory reaction of lung tissues in mice without (left) and with asthma (right) (×100).
Figure 2
Figure 2
Histopathological score of lung tissues in mice without and with asthma. Tissue inflammation was scored as described in [18].
Figure 3
Figure 3
AHR of lung tissues in mice without and with asthma, as measured by unrestrained plethysmography.

References

    1. Kay AB. Allergy and allergic diseases. First of two parts. N Engl J Med. 2001;344:30–37. - PubMed
    1. Dechene L. TH1/TH2 immune response. J Allergy Clin Immunol. 2002;10:539–540. - PubMed
    1. Hansen G, Berry G, DeKruyff RH, Umetsu DT. Allergen-specific Th1 cells fail to counterbalance Th2 cell-induced airway hyper reactivity but cause severe airway inflammation. J Clin Invest. 1999;103:175–83. - PMC - PubMed
    1. Sackesen C, Birben E, Soyer OU, Sahiner UM, Yavuz TS, Civelek E, Karabulut E, Akdis M, Akdis CA, Kalayci O. The effect of CD14C159T polymorphism on in vitro IgE synthesis and cytokine production by PBMC from children with asthma. Allergy. 2011;66:48–57. - PubMed
    1. Krug N, Madden J, Redington AE, Lackie P, Djukanovic U. T-cell cytokine profile evaluated at the single cell level in BAL and blood in allergic asthma. Am J Respir Cell Mol Biol. 1996;14:319–326. - PubMed