Zhou Jianhui, Lottenbach Kathleen R, Barenkamp Stephen J, Reason Donald C
Children's Hospital Oakland Research Institute, Oakland, California 94609, USA.
Infect Immun. 2004 Jun;72(6):3505-14. doi: 10.1128/IAI.72.6.3505-3514.2004.
Combinatorial cloning and expression library analysis were used to determine the expressed human antibody repertoire specific for the capsular polysaccharide (PS) of Streptococcus pneumoniae serotype 6B. Sequence analysis of 55 6B-specific antibody Fab fragments isolated from six vaccinated donors reveal that different individuals used a variety of heavy and light chain germ line variable (V) region genes to form pneumococcal capsular PS (PPS) 6B-specific paratopes. Within each donor, however, the response was more restricted, with five of the six donors using at most one or two gene pairs to form combining sites. Analysis also indicated that although the response in each donor was oligoclonal in terms of variable gene usage, the combination of extensive somatic hypermutation, deletion of germ line-encoded residues, insertion of non-germ line-encoded residues, and intraclonal isotype switching generated a surprising degree of paratope diversity within the individuals analyzed. In contrast to previously studied PS-specific responses, we find that the PPS 6B repertoire makes use of a diverse collection of heavy-chain and light-chain V region gene products to form specific paratopes, with no apparent tendency for conservation of immunoglobulin gene usage between individuals.
采用组合克隆和表达文库分析来确定针对肺炎链球菌6B血清型荚膜多糖(PS)的人源抗体库。对从6名接种疫苗的供体中分离出的55个6B特异性抗体Fab片段进行序列分析,结果显示不同个体使用多种重链和轻链种系可变(V)区基因来形成肺炎球菌荚膜PS(PPS)6B特异性互补决定区。然而,在每个供体内,反应更为局限,6名供体中有5名最多使用一对或两对基因对来形成结合位点。分析还表明,尽管每个供体的反应在可变基因使用方面是寡克隆的,但广泛的体细胞超突变、种系编码残基的缺失、非种系编码残基的插入以及克隆内同种型转换的组合在分析的个体中产生了惊人程度的互补决定区多样性。与之前研究的PS特异性反应不同,我们发现PPS 6B抗体库利用多种重链和轻链V区基因产物来形成特异性互补决定区,个体之间在免疫球蛋白基因使用上没有明显的保守倾向。