Effect of interleukin-33 on Th1/Th2 cytokine ratio in peripheral lymphocytes in asthmatic mice.
- Author:
Xinliang HE
1
;
Wei WU
1
;
Yan LU
1
;
Yali GUO
1
;
Chaoliang HU
1
;
Yuyun HUANG
1
;
Yuzu XU
1
;
Jungang XIE
1
;
Jianping ZHAO
2
Author Information
- Publication Type:Journal Article
- MeSH: Animals; Asthma; chemically induced; immunology; metabolism; Enzyme-Linked Immunosorbent Assay; Female; Interferon-gamma; immunology; metabolism; Interleukin-33; Interleukin-5; immunology; metabolism; Interleukins; immunology; metabolism; Lymphocytes; immunology; metabolism; Mice; Mice, Inbred BALB C
- From: Chinese Medical Journal 2014;127(8):1517-1522
- CountryChina
- Language:English
-
Abstract:
BACKGROUNDAllergic asthma is a chronic airway inflammatory disease partly characterised by high concentration of T help 2 (Th2) cytokines in bronchoalveolar lavage fluid (BALF). There is no report on the relation of peripherally circulating blood lymphocytes and asthma. We explored the balance of Th2/Th1 cytokines in asthmatic mice. Exogenous recombinant interleukin (IL) 33 acted on murine peripheral circulating blood lymphocytes, IL-5 cytokine was selected for assessing Th2 cytokines and interferon-gamma (IFN-γ) for Th1 cytokines.
METHODSFemale specific pathogen free BABL/c mice were sensitised by intraperitoneal injection of 20 µg of ovalbumin emulsified in 1 mg of aluminium hydroxide gel in a total volume of 200 µl, and challenged for 30 minutes in 7 consecutive days with an aerosol of 2 g ovalbumin in 100 ml of PBS. Then we collected BALF and isolated lymphocytes from the peripheral blood. The lymphocytes were divided into two groups: asthmatic group and normal group. Th1/Th2 cytokines was detected by enzyme-linked immunosorbent assay (ELISA) kits.
RESULTSIn the asthma group, we found numerous eosinophils and lymphocytes on the glass slides. We then confirmed that the optimal concentration of IL-33 was 10 ng/ml and time of IL-33 stimulating lymphocytes was 24 hours. In the asthma group, the production of IL-5 was significantly increased over normal group after stimulation with IL-33 (P < 0.05) and the production of IFNγ was supressed from IL-33 stimulated lymphocytes (P < 0.05).
CONCLUSIONIL-33 acts on lymphocytes of peripheral blood increasing secretion of Th2 cytokines and inhibiting secretion of Th1 cytokines.