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在健康的巨细胞病毒(CMV)血清阴性受试者中,用CMV糖蛋白B(gB)免疫后未诱导出自体抗体反应。

Lack of induction of autoantibody responses following immunization with cytomegalovirus (CMV) glycoprotein B (gB) in healthy CMV-seronegative subjects.

作者信息

Schleiss Mark R, Bernstein David I, Passo Murray, Parker Susan, Meric Claude, Verdier François, Newkirk Marianna M

机构信息

Division of Infectious Diseases, 3333 Burnet Avenue, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.

出版信息

Vaccine. 2004 Dec 16;23(5):687-92. doi: 10.1016/j.vaccine.2004.06.038.

DOI:10.1016/j.vaccine.2004.06.038
PMID:15542191
Abstract

Possible correlations have been proposed between autoimmune diseases, such as systemic lupus erythematosus (SLE), and infection with human cytomegalovirus (CMV). The recent observation that an adenovirus expressing the immunodominant envelope glycoprotein of CMV, glycoprotein B (gB), may be capable of inducing autoantibodies in certain mouse strains has prompted interest in exploring potential relationships between gB immunization and autoimmune disease. We examined whether a recombinant CMV gB vaccine, or a gB canarypox vectored vaccine (ALVAC-CMVgB), administered to a total of 76 CMV-seronegative subjects, was capable of inducing cross-reactive antibodies to Smith antigen (Sm), ribonucleoprotein complex (RNP), and the U1-70 kDa component of the RNP complex. Using immunofluorescence, EIA and immunoblot analyses, we failed to identify induction of autoantibodies following vaccination with gB, whether administered alone as a purified protein subunit with adjuvant, or in combination with expression in a vectored approach using a recombinant canarypox. These data reinforce the favorable safety profile of CMV gB vaccines.

摘要

自身免疫性疾病,如系统性红斑狼疮(SLE),与人巨细胞病毒(CMV)感染之间可能存在相关性。最近观察到,一种表达CMV免疫显性包膜糖蛋白糖蛋白B(gB)的腺病毒可能能够在某些小鼠品系中诱导自身抗体,这引发了人们对探索gB免疫与自身免疫性疾病之间潜在关系的兴趣。我们研究了给予总共76名CMV血清阴性受试者的重组CMV gB疫苗或gB金丝雀痘病毒载体疫苗(ALVAC-CMVgB)是否能够诱导针对史密斯抗原(Sm)、核糖核蛋白复合物(RNP)以及RNP复合物的U1-70 kDa成分的交叉反应性抗体。通过免疫荧光、酶免疫分析和免疫印迹分析,我们未能确定接种gB后是否会诱导自身抗体,无论gB是作为纯化的蛋白亚基与佐剂单独给药,还是与重组金丝雀痘病毒载体表达联合给药。这些数据强化了CMV gB疫苗良好的安全性。

相似文献

1
Lack of induction of autoantibody responses following immunization with cytomegalovirus (CMV) glycoprotein B (gB) in healthy CMV-seronegative subjects.在健康的巨细胞病毒(CMV)血清阴性受试者中,用CMV糖蛋白B(gB)免疫后未诱导出自体抗体反应。
Vaccine. 2004 Dec 16;23(5):687-92. doi: 10.1016/j.vaccine.2004.06.038.
2
Effect of previous or simultaneous immunization with canarypox expressing cytomegalovirus (CMV) glycoprotein B (gB) on response to subunit gB vaccine plus MF59 in healthy CMV-seronegative adults.在健康的巨细胞病毒血清阴性成年人中,先前或同时接种表达巨细胞病毒(CMV)糖蛋白B(gB)的金丝雀痘病毒对亚单位gB疫苗加MF59免疫反应的影响。
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A canarypox vector expressing cytomegalovirus (CMV) glycoprotein B primes for antibody responses to a live attenuated CMV vaccine (Towne).一种表达巨细胞病毒(CMV)糖蛋白B的金丝雀痘病毒载体可引发针对减毒活CMV疫苗(汤氏疫苗)的抗体反应。
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The genotype of mice influences the autoimmune response to spliceosome proteins induced by cytomegalovirus gB immunization.小鼠的基因型影响巨细胞病毒gB免疫诱导的对剪接体蛋白的自身免疫反应。
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Detection of cytomegalovirus infection during clinical trials of glycoprotein B vaccine.糖蛋白B疫苗临床试验期间巨细胞病毒感染的检测
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Human anti-nuclear ribonucleoprotein antigen autoimmune sera contain a novel subset of autoantibodies that stabilizes the molecular interaction of U1RNP-C protein with the Sm core proteins.人抗核糖核蛋白抗原自身免疫血清含有一类新型自身抗体,这类抗体可稳定U1RNP-C蛋白与Sm核心蛋白的分子相互作用。
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Autoimmune response to U1 small nuclear ribonucleoprotein (U1 snRNP) associated with cytomegalovirus infection.与巨细胞病毒感染相关的针对U1小核糖核蛋白(U1 snRNP)的自身免疫反应。
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A subunit cytomegalovirus vaccine based on recombinant envelope glycoprotein B and a new adjuvant.一种基于重组包膜糖蛋白B和新型佐剂的亚单位巨细胞病毒疫苗。
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Cytomegalovirus infection in pediatric rheumatic diseases: a review.儿童风湿性疾病中的巨细胞病毒感染:综述。
Pediatr Rheumatol Online J. 2010 May 20;8:17. doi: 10.1186/1546-0096-8-17.
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