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Different Somatic Hypermutation Levels among Antibody Subclasses Disclosed by a New Next-Generation Sequencing-Based Antibody Repertoire Analysis

机译:新的基于下一代测序的抗体库分析揭示的抗体亚类之间不同的体细胞超突变水平

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A diverse antibody repertoire is primarily generated by the rearrangement of V, D, and J genes and subsequent somatic hypermutation (SHM). Class-switch recombination (CSR) produces various isotypes and subclasses with different functional properties. Although antibody isotypes and subclasses are considered to be produced by both direct and sequential CSR, it is still not fully understood how SHMs accumulate during the process in which antibody subclasses are generated. Here, we developed a new next-generation sequencing (NGS)-based antibody repertoire analysis capable of identifying all antibody isotype and subclass genes and used it to examine the peripheral blood mononuclear cells of 12 healthy individuals. Using a total of 5,480,040 sequences, we compared percentage frequency of variable (V), junctional (J) sequence, and a combination of V and J, diversity, length, and amino acid compositions of CDR3, SHM, and shared clones in the IgM, IgD, IgG3, IgG1, IgG2, IgG4, IgA1, IgE, and IgA2 genes. The usage and diversity were similar among the immunoglobulin (Ig) subclasses. Clonally related sequences sharing identical V, D, J, and CDR3 amino acid sequences were frequently found within multiple Ig subclasses, especially between IgG1 and IgG2 or IgA1 and IgA2. SHM occurred most frequently in IgG4, while IgG3 genes were the least mutated among all IgG subclasses. The shared clones had almost the same SHM levels among Ig subclasses, while subclass-specific clones had different levels of SHM dependent on the genomic location. Given the sequential CSR, these results suggest that CSR occurs sequentially over multiple subclasses in the order corresponding to the genomic location of IGHCs, but CSR is likely to occur more quickly than SHMs accumulate within Ig genes under physiological conditions. NGS-based antibody repertoire analysis should provide critical information on how various antibodies are generated in the immune system.
机译:多种抗体库主要是由V,D和J基因的重排以及随后的体细胞超突变(SHM)产生的。类开关重组(CSR)产生具有不同功能特性的各种同种型和子类。尽管认为抗体同种型和亚类是由直接和顺序CSR产生的,但仍不完全了解SHM在抗体亚类生成过程中如何积累。在这里,我们开发了一种新的基于下一代测序(NGS)的抗体库分析,能够识别所有抗体同种型和亚类基因,并将其用于检查12位健康个体的外周血单核细胞。使用总共5,480,040个序列,我们比较了可变(V),连接(J)序列以及V和J的组合的频率百分比,CDR3,SHM的多样性,长度和氨基酸组成以及IgM中的共享克隆,IgD,IgG3,IgG1,IgG2,IgG4,IgA1,IgE和IgA2基因。免疫球蛋白(Ig)亚类之间的用法和多样性相似。在多个Ig亚类中,尤其是在IgG1和IgG2或IgA1和IgA2之间,经常发现具有相同的V,D,J和CDR3氨基酸序列的克隆相关序列。在IgG4中,SHM最常见,而在所有IgG亚类中,IgG3基因的突变最少。 Ig子类之间共享的克隆具有几乎相同的SHM水平,而子类特异性克隆则取决于基因组位置,具有不同的SHM水平。给定连续的CSR,这些结果表明CSR在多个子类上按与IGHCs基因组位置相对应的顺序依次发生,但是在生理条件下,CSR发生的速度可能比SHg在Ig基因内积累的速度更快。基于NGS的抗体库分析应提供有关免疫系统中如何产生各种抗体的关键信息。

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