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粒细胞巨噬细胞集落刺激因子(GM-CSF)可诱导终末期肾衰竭患者对乙肝疫苗无应答者产生血清保护作用。

Granulocyte macrophage colony stimulating factor (GM-CSF) induced sero-protection in end stage renal failure patients to hepatitis B in vaccine non-responders.

作者信息

Jha R, Lakhtakia S, Jaleel M A, Narayan G, Hemlatha K

机构信息

Department of Nephrology, Medwin Hospitals, Hyderabad, Andhra Pradesh, India.

出版信息

Ren Fail. 2001 Sep;23(5):629-36. doi: 10.1081/jdi-100107359.

DOI:10.1081/jdi-100107359
PMID:11725909
Abstract

Hepatitis B (HB) virus infection is a major health problem in dialysis dependent end stage renal failure (ESRF) patients. The sero-conversion rate after recombinant HB vaccine in ESRF patients is poor. Adjuvants like Granulocyte Macrophage-Colony Stimulating Factor (GM-CSF) have been found to improve response rate to vaccines. This study was conducted to evaluate the efficacy of GM-CSF as an adjuvant to HB vaccine in ESRF patients who were non-responders to the usual three double dose vaccinations (primary non-responders). Fifty consecutive HBsAg negative and anti-HBs negative ESRF patients on hemodialysis over thirty months were prospectively included (Jan. 96-June 98). All received 40 microg of recombinant HB vaccine at 0, 1, 2 month interval. Anti-HBs titres were subsequently tested after four weeks of the third dose. There were 19 (38%) primary non-responders (antiHBs negative). Twelve (Group I) of primary non-responders were given an additional dose of HB vaccine with 300 microg (5-6 microg/kg) of GM-CSF (Leucomax) and the remaining seven (Group II) received only an additional dose of HB vaccine. Anti-HBs was determined by Abbott's ELISA kit, and titre above 10 mIU/mL was considered as protective. In Group I, sero-protective titres were obtained in 11 out of 12 (91.6%) patients, whereas in Group II none of the patients achieved sero-protection (p < 0.001). The sero-conversion rate improved from initial 62% (31/50) to overall 84% (42/150) after the use of GM-CSF. There were no adverse events noted with the use of GM-CSF. At one year, 24 out of 32 (75%) who were sero-protected earlier continued to remain sero-protected. This study indicates that GM-CSF is a potent HB vaccine adjuvant for sero-conversion in primary non-responders.

摘要

乙型肝炎(HB)病毒感染是依赖透析的终末期肾衰竭(ESRF)患者面临的一个主要健康问题。ESRF患者接种重组HB疫苗后的血清转化率较低。已发现粒细胞巨噬细胞集落刺激因子(GM-CSF)等佐剂可提高对疫苗的反应率。本研究旨在评估GM-CSF作为佐剂对常规三次双剂量接种无反应(原发性无反应者)的ESRF患者接种HB疫苗的疗效。前瞻性纳入了连续50例在30个月内接受血液透析的HBsAg阴性和抗-HBs阴性的ESRF患者(1996年1月至1998年6月)。所有患者均在0、1、2个月间隔时接种40微克重组HB疫苗。在第三剂接种四周后检测抗-HBs滴度。有19例(38%)原发性无反应者(抗-HBs阴性)。12例(第一组)原发性无反应者额外接种一剂HB疫苗,并加用300微克(5-6微克/千克)GM-CSF(沙格司亭),其余7例(第二组)仅额外接种一剂HB疫苗。采用雅培ELISA试剂盒测定抗-HBs,滴度高于10 mIU/mL被视为具有保护性。在第一组中,12例患者中有11例(91.6%)获得了血清保护性滴度,而第二组中无一例患者实现血清保护(p<0.001)。使用GM-CSF后,血清转化率从最初的62%(31/50)提高到总体的84%(42/50)。使用GM-CSF未观察到不良事件。一年后,早期具有血清保护作用的32例患者中有24例(75%)继续保持血清保护。本研究表明,GM-CSF是原发性无反应者血清转化的一种有效的HB疫苗佐剂。

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