期刊文献+

Hepatitis B-specific T helper cell responses in uninfected infants born to HBsAg^(+)/HBeAg^(-) mothers 被引量:4

原文传递
导出
摘要 Vertically transmitted hepatitis B virus(HBV)usually causes chronic infection.While combined active–passive immunoprophylaxis in neonates of hepatitis B surface antigen-positive(HBsAg1)mothers at birth prevents vertical transmission,it is not yet clear whether neonates encounter the virus or its products in the absence of hepatitis B e antigen(HBeAg).This study was undertaken to investigate HBV antigen-specific T-cell responses in vaccinated neonates of HBsAg1/HBeAg2 mothers.Blood was collected from 46 HBsAg1 mothers and their neonates(subjects)as well as 24 age-matched controls.All neonates of HBsAg1 mothers received appropriate immunoprophylaxis,and HBsAg and hepatitis B surface antibody(anti-HBs)antibody titers were determined after completion of the vaccination course.Peripheral blood mononuclear cells(PBMCs)from infants at birth,1 and 6 months of age were stimulated with recombinant HBsAg,hepatitis B core antigen(HBcAg)and mitogen,and interferon(IFN)-c concentrations were determined by ELISA.HBsAg-induced production of IL-2,IL-5,IL-6 and IL-10 was assessed using a cytometric bead array kit on cells from 6-month-old neonates post-vaccination.All neonates were HBsAg2 and responded to vaccination.Increased IFN-c production following HBcAg stimulation was seen in 30.4%of neonates born to HBsAg1/HBeAg2 mothers.Subjects demonstrated significantly higher IL-2 production post-HBsAg stimulation,whereas IL-5,IL-6 and IL-10 cytokine responses were not significantly different.Almost one-third of uninfected neonates developed viral antigen-induced IFN-c production,suggesting that they had been exposed to virions or viral derivatives.This encounter,however,did not impair their T-cell responses to vaccination.
出处 《Cellular & Molecular Immunology》 SCIE CAS CSCD 2010年第6期454-458,共5页 中国免疫学杂志(英文版)
  • 相关文献

参考文献1

二级参考文献15

  • 1Chisari FV. Cytotoxic T cells and viral hepatitis. J Clin Invest 1997; 99:1472-1477.
  • 2Hart DN. Dendritic cells: unique leukocyte population which control the primary immune response. Blood 1997; 90: 3245-3287.
  • 3Steinman RM. The dendritic cell system and its role in immunogenicity. Annu Rev Immunol 1991; 9:271-296.
  • 4Rescigno M, Granucci F, Ricciardi-Castagnoli P. Dendritic cells at the end of the millelxnium. Immunol Cell Biol 1999; 77:404-410.
  • 5Shimizu Y, Guidotti LG, Fowler P, Chisari FV. Dendritic cell immunization breaks cytotoxic T lymphocyte tolerance in hepatitis B virus transgenic mice. J Immunol 1998; 161:4520-4529.
  • 6Romani N, Reider D, Heuer M, Ebner S, Kampgen E, Eibl B,Niederwieser D, Schuler G. Generation of mature dendritic cells from human blood. An improved method with special regard to clinical applicability, J Immunol Methods 1996; 196:137-151.
  • 7Romani N, Gruner S, Brang D, Kampgen E, Lenz A,Trockenbacher B, Konwalinka G, Fritsch PO, Steinman RM,Schuler G. Proliferating dendritic cell progenitors in human blood. J Exp Med 1994; 180:83-93.
  • 8Akbar SM, Inaba K, Onji M. Upregulation of MHC class Ⅱ antigen on dendritic cells from hepatitis B virus transgeneic mice by interferon-T, abrogation of immune response defect to a T-cell-dependent antigen. Immunology 1996; 87:519-527.
  • 9Freeman GJ, Boussiotis VA, Anumanthan A, Bernstein GM,Ke XY, Rennert PD, Gray GS, Gribben JG, Nadler LM. B7-1and B7-2 do not deliver identical costimulatory signals, since B7-2 but not B7-1 preferentially costimulates the initial production of IL-4. Immunity 1995; 2:523-532.
  • 10Kuchroo VK, Das MP, Brown JA, Ranger AM, Zamvil SS,Sobel RA, Weiner HL, Nabavi N, Glimcher LH. B7-1and B7-2 costimulatory molecules activate differentially the Th1/Th2 developmental pathways: application to autoimmune disease therapy. Cell 1995; 80:707-718.

共引文献7

同被引文献5

引证文献4

二级引证文献51

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