Publication in refereed journal
香港中文大学研究人员 ( 现职)
| 伦慧敏博士 (化学病理学系) |
| 许树昌教授 (内科及药物治疗学系) |
| 梁廷勋教授 (儿科学系) |
| 林伟基教授 (化学病理学系) |
| 司徒卓俊教授 (内科及药物治疗学系) |
| 黄振国教授 (化学病理学系) |
全文
| 数位物件识别号 (DOI) http://dx.doi.org/10.1111/j.1365-2249.2006.03315.x |
引用次数
Web of Sciencehttp://aims.cuhk.edu.hk/converis/portal/Publication/12WOS source URL
其它资讯
摘要T-bet is a novel transcription factor regulating lineage commitment of T helper (Th) lymphocytes to a predominant Th1 phenotype. Previous studies on T-bet and asthma focused mainly on bronchial biopsy specimens. This study assessed the relationship between T-bet expression and levels of selected chemokines in the peripheral blood of asthmatics. Blood was collected from 24 steroid-naive asthmatics, 39 asthmatics on inhaled corticosteroid and 32 age- and sex-matched controls for assay of T-bet expression, specific IgE and chemokines (interferon-gamma inducible protein-10 (IP-10/CXCL10), monokines induced by interferon-gamma (MIG/CXCL9), monocyte chemotactic protein-1 (MCP-1/CCL2), regulated upon activation normal T cell expressed and secreted (RANTES/CCL5) and interleukin-8 (IL-8/CXCL8) levels. T-bet mRNA expression was assessed by real-time quantitative reverse transcription-polymerase chain reaction (RT-PCR). Chemokine levels were assessed by immunofluorescence flow cytometry. The mean (s.d.) age and forced expiratory volume in 1 s (FEV1)% predicted of the asthmatics were 43.6 (14.6) years and 85.9 (20.0)%, respectively. The median (IQR) T-bet expression after normalization with beta-actin was suppressed in asthmatics versus controls [asthmatics 0.71 (0.59) versus controls 1.07 (1.14), P = 0.03].The median (IQR) of plasma RANTES was elevated, whereas IP-10 was suppressed in asthmatics versus controls (RANTES: 13 658.0 (13673.3) versus 6299.5 (19 407.8) pg/ml, P = 0.03; IP-10: 1047.6 (589.8) versus 1306.4 (759.9) pg/ml, P = 0.001). There was a weak and negative correlation between T-bet expression and RANTES level in the asthmatics (r = -0.29, P = 0.032). T-bet could be measured in peripheral blood and its expression was suppressed in asthmatics. This is in keeping with asthma being a predominantly Th2 disease and T-bet probably plays a role in the pathogenesis of asthma. Further studies are needed to explore the potential application of peripheral blood monitoring of T-bet.
着者Ko FWS, Lun SWM, Wong CK, Szeto CC, Lam CWK, Leung TF, Hui DSC
期刊名称Clinical and Experimental Immunology
出版年份2007
月份3
日期1
卷号147
期次3
出版社BLACKWELL PUBLISHING
页次526 - 532
国际标準期刊号0009-9104
电子国际标準期刊号1365-2249
语言英式英语
关键词asthma; chemokines; peripheral blood; T-bet expression
Web of Science 学科类别Immunology; IMMUNOLOGY
