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Characteristics Peripheral Blood IgG and IgM Heavy Chain Complementarity Determining Region 3 Repertoire before and after Immunization with Recombinant HBV Vaccine

机译:重组HBV疫苗免疫前后外周血IgG和IgM重链互补性的特征决定3区库

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摘要

Immunization with recombinant HBV vaccine induces specific immune responses in human causing B lymphocytes to produce protective HBsAb, and to form memory B lymphocytes, thereby facilitating HBV immunity in the body. However, B lymphocytes heterogeneity and characteristics are not fully elucidated. In this study, we conducted high-throughput sequencing of BCR heavy chain CDR3 repertoires in 3 healthy volunteers before and after the third immunization with recombinant HBV vaccine. We used Roche 454 Genome Sequencer FLX system to perform a comparative analysis of IgM and IgG H chain CDR3 repertoires. First, we found that the diversity of IgG H chain CDR3 repertoires was 1/6 of IgM on average. Moreover, after the third immunization with HBV vaccine, the diversity of IgG H chain CDR3 repertoires was 1/26 of IgM on average. Second, we detected relatively high levels of HBsAbs in all the healthy volunteers after immunization with HBV vaccine. The volunteers shared a small number of CDR3 sequences before and after immunization, and among each other. However, we did not find completely identical BCR H chain CDR3 amino acid sequences in these volunteers. Lastly, after immunization with recombinant HBV vaccine, the volunteers showed high frequency of IgG H chain CDR3 amino acid sequences mostly resulting from rearrangements of IGHV, IGHD and IGHJ, suggesting that the mechanism of high frequency CDR3 generation might be associated with the maturation of IgG affinity (somatic hypermutation) during the recombinant HBV vaccine-induced B lymphocyte responses. This study identified the characteristics and changes of BCR CDR3 repertoires before and after immunization with HBV vaccine, and evaluated the performance of the sequencing technology for this application. Our findings provide a basis for further research in B lymphocyte generated HBsAb heterogeneity and monitoring the maintenance of memory B lymphocytes.
机译:重组HBV疫苗免疫后会在人体内引起特异性免疫反应,导致B淋巴细胞产生保护性HBsAb,并形成记忆B淋巴细胞,从而促进体内HBV免疫。但是,B淋巴细胞的异质性和特征尚未完全阐明。在本研究中,我们在第三次使用重组HBV疫苗免疫之前和之后对3名健康志愿者进行了BCR重链CDR3库的高通量测序。我们使用Roche 454 Genome Sequencer FLX系统对IgM和IgG H链CDR3库进行了比较分析。首先,我们发现IgG H链CDR3组成的多样性平均为IgM的1/6。而且,在用HBV疫苗第三次免疫后,IgG H链CDR3组成的多样性平均为IgM的1/26。第二,我们在用HBV疫苗免疫后在所有健康志愿者中检测到相对较高的HBsAb水平。志愿者在免疫前后共享少量的CDR3序列。但是,我们在这些志愿者中没有发现完全相同的BCR H链CDR3氨基酸序列。最后,在用重组HBV疫苗免疫后,志愿者表现出高频率的IgG H链CDR3氨基酸序列,这主要是由于IGHV,IGHD和IGHJ的重排所致,这表明高频CDR3产生的机制可能与IgG的成熟有关。重组HBV疫苗诱导的B淋巴细胞应答过程中的亲和力(体细胞超突变)。这项研究确定了乙肝病毒疫苗免疫前后BCR CDR3组成的特征和变化,并评估了该技术的测序技术性能。我们的发现为进一步研究B淋巴细胞产生的HBsAb异质性和监测记忆B淋巴细胞的维持提供了基础。

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