期刊文献+

IL-10+CDl9+调节性B淋巴细胞在慢性乙型肝炎患者外周血中的表达 被引量:5

Expression of IL-10+ CD19+ regulatory B cells in peripheral blood of patients with chronic hepatitis B infection
原文传递
导出
摘要 目的分析慢性乙型肝炎患者外周血中IL-10+CDl9+调节性B淋巴细胞(Breg)的表达及其免疫调节机制。方法病例对照研究。收集2011年6月-2012年10月常熟市第二人民医院住院患者,急性乙型肝炎(AHB)患者28例,慢性乙型肝炎(CHB)患者31例和健康对照25名。分离外周血单个核细胞(PBMC),经含CpG序列的寡脱氧核苷酸CpGODN2006和佛波醇酯(PMA)体外作用后,流式细胞术分析IL-10+CD19+Breg、CD4+CD25high调节性T淋巴细胞(Treg)的表达及其相关性,ELISA分析培养上清IL-10水平。Mann—WhitneyU检验分析两组问差异,Spearman相关分析两组连续变量问的相关性。结果CHB组外周血Breg[1.28%(1.05%~2.20%)]高于AHB组[0.87%(0.55%一1.22%)]和HCs组[0.89%(0.51%-1.37%)](P值分别为0.001和0.006),AHB和HCs组间差异无统计学意义(P=0.669)。CpGODN2006和PMA作用后CHB组Bregl14.30%(10.70%-16.70%)]较AHB组[10.30%(7.05%~13.30%)]和HCs组[10.40%(6.85%~12.60%)]显著升高(P值分别为0.003和0.001);CHB组Treg[5.80%(4.20%~9.10%)]较AHB组[4.05%(2.53%~5.40%)]和14Cs组[4.50%(2.55%~5.50%)]也显著增高(P值分别为〈0.001和0.005)。AHB和HCs组间差异均无统计学意义(Breg:P=0.796;Treg:P=0.227)。Spenrman相关性分析发现CHB组Breg与Treg存在正相关关系(r=0.50,P=0.004),而AHB和HCs组无此相关性(r=-0.15,P=0.462;r=0.09,P=0.669)。CHB组IL-10表达高于AHB和HCs组(P〈0.001)。AHB和HCs组间差异无统计学意义(P=0.341),Spearman相关性分析表明CHB组IL-10与Breg存在正相关关系(r=0.409,P=0.005)。结论B淋巴细胞Breg和调节性T淋巴细胞在慢性乙型肝炎患者中表达升高,Breg可能通过IL—10的分泌在HBV慢性感染过程中发挥免疫调节作用。 Objective To investigate the population and role of IL-10+ CD19~ regulatory B cell (Breg) in patients with chronic hepatitis B. Methods Patients with acute hepatitis B ( AHB ) ( n = 28 ), chronic hepatitis B (CHB) (n = 31 ) and normal subjects (n =-25) were collected from Changshu No. 2 People's Hospital between 2011 June and 2012 October. Peripheral blood mononuelear cells (PBMC) were isolated and stimulated with CpG ODN 2006 and PMA. Flow cytometry was used to analyze the population of IL-10+CD19+ Breg, CIM+ CD25high Treg, and ELISA was used to analyze the concentration of IL-10 in culture supernatant. Results The population of Breg in Peripheral blood of the CHB group [ 1.28% ( 1.05% -2.20% ) ] was higher than that in the AHB group [0. 87% (0. 55% - 1.22% ) ] and the HCs group [0. 89% (0. 51% -1. 37% ) ] (P =0. 001, 0. 006), and the difference between the AHB group and the HCs group was not statistically significant (P = 0. 669). Breg in the CHB group [ 14. 30% (10. 70% - 16. 70% ) ] was higher than that in the AHB group [ 10. 30% ( 7.05% - 13.30% ) ] and the HCs group [10.40% (6.85% - 12. 60%)] (P =0.003, 0.001), treg in the CHB group [5.80% (4.20% - 9. 10% )] was also higher than that in the AHB group [4. 05% (2. 53% -5.40% )] and the HCs group [4. 50% (2. 55% -5.50% ) ] (P 〈0. 001, P =0. 005), and there was no significantly difference between the AHB group and the HCs group ( Breg: P = 0. 796 ; Treg: P = 0. 227 ). Spearman correlation analysis showed that Breg was positively correlated with Treg in the CHB group ( r = 0. 50, P = 0. 004), however there was no significantly correlation in the AHB group and the HCs group (r = - 0. 15, P = 0. 462 ; r = 0. 09, P = 0. 669). The concentration of IL-10 in the CHB group was higher than that in the AHB group and the HCs group ( P 〈 0. 001 ), and the difference between the AHB group and the HCs group was not statistically significant (P = 0. 341 ). Spe
出处 《中华检验医学杂志》 CAS CSCD 北大核心 2014年第2期100-104,共5页 Chinese Journal of Laboratory Medicine
基金 苏州市科技发展计划应用基础研究项目(SYSD2011011) 常熟市科技发展计划社会发展项目(CS201113)
关键词 肝炎 乙型 慢性 B淋巴细胞 调节性 T淋巴细胞 调节性 白细胞介素10 抗原 CDl9 Hepatitis B chronic B-lymphocytes, regulatoy T-lymphocytes, regulatory Interleukin-10 Antigens, CD19
  • 相关文献

参考文献16

  • 1Lavanchy D. Hepatitis B virus epidemiology, disease burden, treatment, and current and emerging prevention and control measures[J]. J Viral Hepat, 2004, 11 : 97-107. 被引量:1
  • 2Maini MK, Boni C, Ogg GS, et al. Directex vivo analysis of hepatitis B-vires specific CD8 + T cells associated with the control of infection[J]. Gastroenterology, 1999, 117: 1386-1396. 被引量:1
  • 3Webster GJ, Reignat S, Brown D, et al. Longitudinal analysis of CD8 + T cells specific for structural and nonstructural hepatitis B virus proteins in patients with chronic hepatitis B. implications for immunotherapy[J]. J Virol 2004, 78: 5707-5719. 被引量:1
  • 4Mauri C, Gray D, Mushtaq N, et al. Prevention of arthritis by interleukin 10-producing B cells [ J ]. J Exp Med, 2003, 197: 489-501. 被引量:1
  • 5Bouaziz JD, Le Buanec H, Saussine A, et al. IL-10 producing regulatory B cells in mice and humans: state of the art[J]. Curr Mol Med, 2012, 12: 519-527. 被引量:1
  • 6Ronet C, Hauyon-La Torte Y, Revaz-Breton M, et al. Regulatory B ceils shape the development of Th2 immune responses in BALB/ c mice infected with Leishmania major through IL-10 production [J]. J Immunol, 2010, 184: 886-894. 被引量:1
  • 7Carter NA, Rosser EC, Mauri C. Interleukin-10 produced by B cells is crucial for the suppression of Th17/Th1 responses, induction of T regulatory type 1 cells and reduction of collagen- induced arthritis[J]. Arthritis Res Ther , 2012, 14 : R32. 被引量:1
  • 8中华医学会传染病与,寄生虫病学分会,肝病学分会.病毒性肝炎防治方案[J].中华肝脏病杂志,2000,8(6):324-329. 被引量:14010
  • 9Livingston BD, Alexander J, Crimi C, et ah Altered helper T lymphocyte function assoeiated with chronic hepatitis B virus infection and its role in response to therapeutic vaccination in humans[J]. J Immunol, 1999, 162: 3088-3095. 被引量:1
  • 10Bernasconi NL, Traggiai E, Lanzavecchia A. CpG oligodeoxynucteotides discriminately enhance binding capacity of human naive B ceils to Hepatitis B virus epitopes [ J ]. Science, 2002, 298:2199-2202. 被引量:1

共引文献14009

同被引文献74

  • 1Honer Zu Siederdissen C,Cornberg M. The role of HBsAg lev- els in the current management of chronic HBV infection. Ann Gastroenterol, 2014,27:105-112. 被引量:1
  • 2Thimme R,Wieland S,Steiger C,et al. CD8+T cells mediate vi- ral clearance and disease pathogenesis during acute hepatitis B virus infection. J Virol,2003,77(1):68-76. 被引量:1
  • 3Zhang N,Bevan MJ. CD8 (+)T cells:foot soldiers of the im- mune system. Immunity, 2011,35 ( 2 ): 161-168. 被引量:1
  • 4Schuch A,Hoh A,Thimme R. The role of natural killer cells and CD8'T cells in hepatitis B virus infection. Immunology, 2014,258(5):1-8. 被引量:1
  • 5Youngblood B,Hale JS,Ahmed R. T-cell memory differentia- tion:insights from transcriptional signatures and epigeneties. Immunology, 2013,139 ( 3 ) :277 -284. 被引量:1
  • 6Appay V,Van Lier RA,Sallusto F,et al. Phenotype and func- tion of human T lymphocyte subsets:consensus and issues. Cy- tometry A, 2008,73 ( 11 ):975-983. 被引量:1
  • 7Shi CC,Tjwa ET,Biesta PJ,et al. Hepatitis B virus suppresses the functional interaction between natural killer cells and plas- macytoid dendritic cells. J Viral Hepat,2012,19(2):26-33. 被引量:1
  • 8Bertoletti A,Ferrari C. Innate and adaptive immune responses in chronic hepatitis B virus infections:towards restoration of im- mune control of viral infection. Gut,2012,61(12):1754-1764. 被引量:1
  • 9Maini MK,Boni C,Lee CK,et al. The role of virus-specific CD8 (+) cells in liver damage and viral control during persistent hepatitis B virus infection. J Exp Med,2000,191(8):1269-1280. 被引量:1
  • 10Yang BF,Zhao HL,Xue C,et al. Recombinant heat shock pro- tein65 carrying hepatitis B core antigen induces HBeAg-spe- cific CTL response. Vaccine, 2007,25 (22):4478-4486. 被引量:1

引证文献5

二级引证文献12

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部