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1.
Sci Rep ; 8(1): 9816, 2018 06 29.
Article in English | MEDLINE | ID: mdl-29959403

ABSTRACT

Particulate matter (PM) is one of the most important environmental issues in China. This study aimed to explore the correlation between PM2.5 and airway inflammation in healthy rats. The PM2.5 group was given an intranasal instillation of PM2.5 suspension on 15 consecutive days, and each received oral saline from day 16 to 90. The BV intervention group was treated as the PM2.5 exposure group, except that BV instead of saline was given daily. A histopathologic examination was performed to evaluate the airway inflammation. The prevalence and function of Th1/Th2/Treg/Th17 cells were detected by flow cytometry and ELISA. The expression of AhR was detected by western blot and real-time PCR. We found that epithelial damage and increased infiltration of inflammatory cell were present in the airways after PM2.5 exposure; there was an immune imbalance of Th cells in the PM2.5 group; the expression of AhR was increased in the airways after PM2.5 exposure. In the PM2.5 + BV group, we demonstrated alleviated immune imbalance and reduced inflammatory cell infiltration in the airways. Our study showed that exposure to PM2.5 induced airway inflammation. The imbalance of Th1/Th2/Treg/Th17 in PM2.5-induced airway inflammation might be associated with activation of the AhR pathway. Oral BV reduces PM2.5-induced airway inflammation and regulates systemic immune responses in rats.


Subject(s)
Adjuvants, Immunologic/pharmacology , Air Pollutants/adverse effects , Bronchial Hyperreactivity/prevention & control , Cell Extracts/pharmacology , Particulate Matter/adverse effects , Pneumonia/prevention & control , Th17 Cells/immunology , Animals , Bronchial Hyperreactivity/etiology , Bronchial Hyperreactivity/pathology , Pneumonia/etiology , Pneumonia/pathology , Rats
2.
Iran J Allergy Asthma Immunol ; 15(5): 413-419, 2016 Oct.
Article in English | MEDLINE | ID: mdl-27917628

ABSTRACT

Allergic rhinitis (AR) is an IgE-mediated upper airway disease, and its impact on asthma has been widely recognized. Protein tyrosine phosphatase non-receptor 22 (PTPN22) gene and the cytotoxic T-lymphocyte-associated antigen 4 (CTLA-4) gene polymorphisms have been reported to be associated with several immune-related diseases. Here we investigated the reffect of these two genes' polymorphisms on the risk of AR and asthma in Chinese Han children. A total of 106 AR patients, 112 AR with asthma patients, and 109 healthy children were enrolled in the study. The SNPs of PTPN22 (rs2488457, rs1310182, rs3789604) and CTLA-4 (rs3087243, rs11571302, rs11571315, rs231725, rs335219727, and rs4553808) were genotyped using a PCR-restriction fragment length polymorphism assay. For PTPN22, an increased prevalence of the CC genotype and C allele in rs1310182 were identified in AR group. For CTLA-4, AA genotype and A allele in rs3087243 and rs231725 were increased in AR with asthma group while in AR group, AA genotype and A allele in rs231725 were obviously decreased. This study reveals a significant association between SNPs in PTPN22, CTLA-4 gene and AR with asthma in Chinese Han children, which might be susceptibility factors for AR and asthma.


Subject(s)
Asthma/genetics , CTLA-4 Antigen/genetics , Polymorphism, Single Nucleotide , Protein Tyrosine Phosphatase, Non-Receptor Type 22/genetics , Rhinitis, Allergic/genetics , Adolescent , Asian People , Asthma/epidemiology , Asthma/immunology , CTLA-4 Antigen/immunology , Child , Child, Preschool , China/epidemiology , Female , Humans , Infant , Male , Protein Tyrosine Phosphatase, Non-Receptor Type 22/immunology , Rhinitis, Allergic/epidemiology , Rhinitis, Allergic/immunology
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