Department of Immunology, University of Oslo, Oslo, Norway.
K. G. Jebsen Centre for Coeliac Disease Research, University of Oslo and Oslo University Hospital, Oslo, Norway.
Genes Immun. 2021 Aug;22(4):205-217. doi: 10.1038/s41435-021-00145-5. Epub 2021 Jun 26.
Immunoglobulins (Ig) play an important role in the immune system both when expressed as antigen receptors on the cell surface of B cells and as antibodies secreted into extracellular fluids. The advent of high-throughput sequencing methods has enabled the investigation of human Ig repertoires at unprecedented depth. This has led to the discovery of many previously unreported germline Ig alleles. Moreover, it is becoming clear that convergent and stereotypic antibody responses are common where different individuals recognise defined antigenic epitopes with the use of the same Ig V genes. Thus, germline V gene variation is increasingly being linked to the differential capacity of generating an effective immune response, which might lead to varying disease susceptibility. Here, we review recent evidence of how germline variation in Ig genes impacts the Ig repertoire and its subsequent effects on the adaptive immune response in vaccination, infection, and autoimmunity.
免疫球蛋白(Ig)在免疫系统中发挥着重要作用,既可以作为 B 细胞表面抗原受体表达,也可以作为分泌到细胞外液的抗体表达。高通量测序方法的出现使得人们能够以前所未有的深度研究人类 Ig 库。这导致了许多以前未报道的胚系 Ig 等位基因的发现。此外,越来越明显的是,在不同个体使用相同的 Ig V 基因识别特定抗原表位时,趋同和定型的抗体反应是常见的。因此,胚系 V 基因变异与产生有效免疫反应的能力差异越来越相关,这可能导致不同的疾病易感性。在这里,我们回顾了最近的证据,说明 Ig 基因的胚系变异如何影响 Ig 库,并对疫苗接种、感染和自身免疫中的适应性免疫反应产生后续影响。