BGI-Shenzhen, Shenzhen, 518083, China.
Division of Clinical Immunology at the Department of Laboratory Medicine, Karolinska Institutet at Karolinska University Hospital Huddinge, 141 86, Stockholm, Sweden.
J Clin Immunol. 2022 Feb;42(2):375-393. doi: 10.1007/s10875-021-01178-1. Epub 2021 Nov 25.
Both DNA damage response and methylation play a crucial role in antigen receptor recombination by creating a diverse repertoire in developing lymphocytes, but how their defects relate to T cell repertoire and phenotypic heterogeneity of immunodeficiency remains obscure. We studied the TCR repertoire in patients with the mutation in different genes (ATM, DNMT3B, ZBTB24, RAG1, DCLRE1C, and JAK3) and uncovered distinct characteristics of repertoire diversity. We propose that early aberrancies in thymus T cell development predispose to the heterogeneous phenotypes of the immunodeficiency spectrum. Shorter CDR3 lengths in ATM-deficient patients, resulting from a decreased number of nucleotide insertions during VDJ recombination in the pre-selected TCR repertoire, as well as the increment of CDR3 tyrosine residues, lead to the enrichment of pathology-associated TCRs, which may contribute to the phenotypes of ATM deficiency. Furthermore, patients with DNMT3B and ZBTB24 mutations who exhibit discrepant phenotypes present longer CDR3 lengths and reduced number of known pathology-associated TCRs.
DNA 损伤反应和甲基化在抗原受体重组中起着至关重要的作用,通过在发育中的淋巴细胞中产生多样化的库,但它们的缺陷如何与 T 细胞库和免疫缺陷的表型异质性相关仍然不清楚。我们研究了不同基因突变(ATM、DNMT3B、ZBTB24、RAG1、DCLRE1C 和 JAK3)患者的 TCR 库,并揭示了库多样性的独特特征。我们提出,胸腺 T 细胞发育早期的异常使免疫缺陷谱表现出异质性表型。ATM 缺陷患者的 CDR3 长度较短,这是由于在预选 TCR 库中 VDJ 重组过程中核苷酸插入减少所致,以及 CDR3 酪氨酸残基的增加,导致与病理学相关的 TCR 富集,这可能导致 ATM 缺陷的表型。此外,表现出不同表型的 DNMT3B 和 ZBTB24 突变患者具有更长的 CDR3 长度和减少的已知与病理学相关的 TCR 数量。