| Literature DB >> 26840774 |
Jiling Ren1, Lizhi Hu1, Jing Yang2, Liang Yang3, Fei Gao1, Ping Lu1, Mengyu Fan1, Yunjuan Zhu1, Junyan Liu1, Lingling Chen1, Shimpy Gupta4, Xi Yang1,5, Peimei Liu1.
Abstract
Allergic asthma is a chronic inflammatory disease mediated by Th2 cell immune responses. Currently, immunotherapies based on immune deviation are attractive, preventive, and therapeutic strategies for asthma. Many studies have shown that intracellular bacterial infections such as mycobacteria and their components can suppress asthmatic reactions by enhancing Th1 responses, while helminth infections and their proteins can inhibit allergic asthma via immune regulation. However, some helminth proteins such as SmP40, the major egg antigen of Schistosoma mansoni, are found as Th1 type antigens. Using a panel of overlapping peptides, we identified T-cell epitopes on SjP40 protein of Schistosoma japonicum, which can induce Th1 cytokine and inhibit the production of Th2 cytokines and airway inflammation in a mouse model of allergic asthma. These results reveal a novel form of immune protective mechanism, which may play an important role in the modulating effect of helminth infection on allergic asthmatic reactions.Entities:
Keywords: Asthma; Schistosoma japonicum; SjP40; Th1 epitope; peptides
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Year: 2016 PMID: 26840774 DOI: 10.1002/eji.201545775
Source DB: PubMed Journal: Eur J Immunol ISSN: 0014-2980 Impact factor: 5.532