期刊文献+

Efficacy of hepatitis B immunoglobulin in relation to the gene polymorphisms of human leukocyte Fcy receptor Ⅲ (CD16) in Chinese liver transplant patients 被引量:4

Efficacy of hepatitis B immunoglobulin in relation to the gene polymorphisms of human leukocyte Fcy receptor Ⅲ (CD16) in Chinese liver transplant patients
原文传递
导出
摘要 Background Although the use of hepatitis B immunoglobulin (HBIG) may lead to a significant reduction in recurrent hepatitis B virus (HBV) infection and improve the survival of patients who have undergone liver transplantation (LT) for hepatitis B-related diseases, the recurrence of the disease still remains at a lower level. Different clinical curative effects were observed in patients with the same HBV-related diseases and the same therapy. This study was undertaken to investigate whether the efficacy of HBIG is associated with FCGR3A gene polymorphisms in Chinese liver transplant patients. Methods Altogether 77 patients who had received liver transplantation for hepatitis B-related diseases with more than one-year survival after surgery were studied. The recurrence of HBV was characterized by the appearance of HBsAg in serum after the operation. The FCGR3A genotyping was performed using genomic DNA sequencing (ABI 3037). Single nucleotide polymorphism at nucleotide 559 was detected by Polyphred. Results Of the 77 patients, 14 were complicated with HBV recurrence post-transplant. The FCGR3A at nucleotide 559 TT was observed in 35 (45.5%0) subjects, whereas TG in 31(40.3%) and GG in 11(14.3%). In the 559G carrier group (n=42, 54.5%), the risk of HBV recurrence was 9.5%, and 1- and 2-year recurrence-free survival rates were 95.2% and 88.7%, respectively. In the 559G noncarrier group (n=35, 45.5%), the risk of HBV recurrence was 28.6%, and 1- and 2-year recurrence-free survival rates were 74.3% and 69.3%, respectively. The risk of HBV recurrence and the recurrence-free survival rate were both statistically different between the 559G carrier and noncarrier groups (P〈0.05). Conclusions A single nucleotide polymorphism (T/G) at position 559 of the FCGR3A gene was found in Chinese patients. The efficacy of HBIG in prophylaxis of HBV recurrence after LT is associated with the gene polymorphism, so detectina FCGR3A aenotypes can be a clinical reference, of the HBIG administration. Background Although the use of hepatitis B immunoglobulin (HBIG) may lead to a significant reduction in recurrent hepatitis B virus (HBV) infection and improve the survival of patients who have undergone liver transplantation (LT) for hepatitis B-related diseases, the recurrence of the disease still remains at a lower level. Different clinical curative effects were observed in patients with the same HBV-related diseases and the same therapy. This study was undertaken to investigate whether the efficacy of HBIG is associated with FCGR3A gene polymorphisms in Chinese liver transplant patients. Methods Altogether 77 patients who had received liver transplantation for hepatitis B-related diseases with more than one-year survival after surgery were studied. The recurrence of HBV was characterized by the appearance of HBsAg in serum after the operation. The FCGR3A genotyping was performed using genomic DNA sequencing (ABI 3037). Single nucleotide polymorphism at nucleotide 559 was detected by Polyphred. Results Of the 77 patients, 14 were complicated with HBV recurrence post-transplant. The FCGR3A at nucleotide 559 TT was observed in 35 (45.5%0) subjects, whereas TG in 31(40.3%) and GG in 11(14.3%). In the 559G carrier group (n=42, 54.5%), the risk of HBV recurrence was 9.5%, and 1- and 2-year recurrence-free survival rates were 95.2% and 88.7%, respectively. In the 559G noncarrier group (n=35, 45.5%), the risk of HBV recurrence was 28.6%, and 1- and 2-year recurrence-free survival rates were 74.3% and 69.3%, respectively. The risk of HBV recurrence and the recurrence-free survival rate were both statistically different between the 559G carrier and noncarrier groups (P〈0.05). Conclusions A single nucleotide polymorphism (T/G) at position 559 of the FCGR3A gene was found in Chinese patients. The efficacy of HBIG in prophylaxis of HBV recurrence after LT is associated with the gene polymorphism, so detectina FCGR3A aenotypes can be a clinical reference, of the HBIG administration.
出处 《Chinese Medical Journal》 SCIE CAS CSCD 2007年第18期1606-1610,共5页 中华医学杂志(英文版)
基金 the State Key Basic Research and Development Program of China(973,No.2003CB515500) the Natural Science Foundation of Zhejiang Province (No. 2004C33108).
关键词 Fc gamma RIII POLYMORPHISM IMMUNOGLOBULIN hepatitis B RECURRENCE Fc gamma RIII polymorphism immunoglobulin hepatitis B recurrence
  • 相关文献

参考文献10

  • 1Samuel D,Muller R,Alexander G,Fassati L,Ducot B,Benhamou JP,et al.Liver transplantation in European patients with the hepatitis B surface antigen[].The New England Journal of Medicine.1993
  • 2Konig V,Hopf U,Neuhaus P,et al.Long-term follow-up of hepatitis B virus-infected recipients after orthotopic liver transplantation[].Transplantation.1994
  • 3Terrault NA,Zhou S,Combs C,Hahn JA,Lake JR,Roberts JP,et al.Prophylaxis in liver transplant recipients using a fixed dosing schedule of hepatitis B immunoglobulin[].Hepatology.1996
  • 4Steinmuller T,Seehofer D,Rayes N,et al.Increasing applicability of liver transplantation for patients with hepatitis B-related liver disease[].Hepatology.2002
  • 5Mohanty SR,Cotler SJ.Management of Hepatitis B in liver transplant patients[].Journal of Clinical Gastroenterology.2005
  • 6Zheng SS,Chen YM,Liang TB,et al.Prevention of Hepatitis B Recurrence After Liver Transplantation Using Lamivudine or Lamivudine Combined With Hepatitis B Immunoglobulin Prophylaxis[].Liver Transplantation.2006
  • 7Bertoletti,A,Ferrari,C,Fiaccadori,F,Penna,A,Margolskee,R,Schlicht,HJ,Fowler,P,Guilhot,S,Chisari,FV.HLA class I-restricted human cytotoxic T cells recognize endogenously synthesized hepatitis B virus nucleocapsid antigen[].Proceedings of the National Academy of Sciences of the United States of America.1991
  • 8Lanier LL,Yu G,Phillips JH.Analysis of Fc gamma RIII (CD 16) membrane expression and association with CD3 zeta and FceRI-gamma by site-directed mutation[].J Immunol.1991
  • 9Ravetch,JV,Perussia,B.Alternative membrane forms of FcγRIII (CD16) on human natural killer cells and neutrophils[].The Journal of Experimental Medicine.1989
  • 10Ory,PA,Goldstein,IM,Kwoh,EE,Clarkson,SB.Characterization of polymorphic forms of Fc receptor III on human neutrophils[].The Journal of Clinical Investigation.1989

同被引文献4

引证文献4

二级引证文献15

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