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分泌人IgA和IgM的肠道浆细胞携带高度突变的VH区域基因。

Human IgA- and IgM-secreting intestinal plasma cells carry heavily mutated VH region genes.

作者信息

Fischer M, Küppers R

机构信息

Institute for Genetics, University of Cologne, Germany.

出版信息

Eur J Immunol. 1998 Sep;28(9):2971-7. doi: 10.1002/(SICI)1521-4141(199809)28:09<2971::AID-IMMU2971>3.0.CO;2-3.

Abstract

Single IgA- or IgM-secreting plasma cells were isolated from histological sections of human jejunum and terminal ileum, and Ig heavy chain variable (VH) region genes were amplified and sequenced. Taken together, 62 of 63 cells analyzed harbored somatically mutated VH region genes, indicating that the vast majority of both IgA- and IgM-secreting intestinal plasma cells derive from germinal center B cells. On average, rearranged VH genes of IgA- and IgM-secreting plasma cells showed a mutation frequency of 9.0 % and 8.5 %, respectively, which exceeds the level of somatic mutation of V region genes carried by human memory B cells. Moreover, we detected deletions or insertions in the complementarity-determining regions of 5 of the 58 functional VH region genes analyzed, suggesting that these alterations may contribute to the diversification of the human antibody repertoire in the course of an immune reaction.

摘要

从人空肠和回肠末端的组织切片中分离出分泌单一IgA或IgM的浆细胞,对Ig重链可变(VH)区基因进行扩增和测序。综合来看,分析的63个细胞中有62个含有体细胞突变的VH区基因,这表明绝大多数分泌IgA和IgM的肠道浆细胞来源于生发中心B细胞。平均而言,分泌IgA和IgM的浆细胞重排VH基因的突变频率分别为9.0%和8.5%,超过了人类记忆B细胞携带的V区基因的体细胞突变水平。此外,我们在分析的58个功能性VH区基因中的5个基因的互补决定区检测到缺失或插入,表明这些改变可能在免疫反应过程中促进人类抗体库的多样化。

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