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2008年07月18日

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2008年07月18日

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2008年07月18日

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2005年05月21日

【期刊论文】Eects of allergen inhalation and oral glucocorticoid on serum soluble CTLA-4 in allergic asthmatics

施焕中, X.-J. Qin, H.-Z. Shi, S.-M. Qin, L.-F. Kang, C.-P. Huang, X.-N. Zhong

,-0001,():

-1年11月30日

摘要

allergen, asthma, glucocorticoid, serum,, soluble CTLA-4.,

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2006年10月27日

【期刊论文】CD28/CTLA-4-CD80/CD86 and ICOS-B7RP-1 costimulatory pathway in bronchial asthma

施焕中, Y.-Q. Chen, H.-Z. Shi

,-0001,():

-1年11月30日

摘要

Costimulatory molecules are cell surface glycoproteins that can direct, modulate and fine-tune T-cell receptor signals. The B7-1/B7-2-CD28/CTLA-4 and ICOS-B7RP-1 pathway provides key second signals that can regulate the activation, inhibition and fine-tuning of T-lymphocyte responses. The expression of B7-1/ B7-2-CD28/CTLA-4 molecules on clinical samples from patients with asthma have been well studied, and the results indicate that different extents of these molecules are expressed on the surface of various cells, and that the concentrations of soluble form of these molecules are elevated in the sera of patients with asthma. There is a burst of papers describing an important role for B7-1/B7-2-CD28/CTLA-4 pathway in the Th1/Th2 balance. Similarly, ICOS stimulates both Th1 and Th2 cytokine production but may have a preferential role in Th2 cell development. Moreover, The B7-1/B7-2-CD28/CTLA-4 and ICOS-B7RP-1 pathway has been suggested of being involved in the development of airway inflammation and airway hyperresponsiveness. Further study of the functions of the pathways within the CD28/CTLA-4-CD80/CD86 and ICOS-B7RP-1 superfamily individually and their interplay should provide insights into the pathogenesis of asthma, and has great therapeutic potential for treatment of asthma.

asthma, costimulation, cytokines, pathogenesis, Tcells.,

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  • 施焕中 邀请

    华中科技大学,湖北

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