Piao Wenji, Grosse Jens, Czwalinna Andreas, Ivanyi Philipp, Ganser Arnold, Franzke Anke
Department of Hematology, Hemostaseology and Oncology, Hannover Medical School, Germany.
Exp Hematol. 2005 Jul;33(7):804-10. doi: 10.1016/j.exphem.2005.04.002.
Acquired aplastic anemia (AA) is a rare disorder characterized by pancytopenia and hypocellular bone marrow. Though experimental and clinical data suggest that AA represents a T cell-mediated disease, neither the immune response nor the nature of inciting antigen(s) have been characterized so far. The identification of a restricted T cell repertoire by PCR techniques in total lymphocyte populations supports an antigen-driven T cell response. In order to investigate the clonal composition, we analyzed the gene rearrangements of the T cell receptor (TCR) variable beta chain (Vbeta) at the single-cell level.
CD3(+) T lymphocytes were micromanipulated from peripheral blood and bone marrow samples of 8 AA patients and healthy controls. Subsequently amplified VDJ gene segments of the TCRVbeta chain were analyzed for functional rearrangements. More than 500 functionally rearranged TCR loci were studied for Vbeta/Jbeta gene segment usage and molecular composition of the complementary-determining region 3 (CDR3).
In comparison to healthy controls, the Vbeta sequences confirmed a highly restricted T cell repertoire in AA patients at the single-cell level. Both in bone marrow and peripheral blood a predominance of Vbeta13 and Jbeta2S7 was observed. Furthermore, individual clonal T-cell expansion was identified in the majority of patients. However, deduced CDR3 amino acid sequences revealed a high variability without common motifs among the 8 patients.
Individual clonal T-cell expansion with high diversity of the antigen-binding sites among the analyzed patients argues for the predominance of private inciting epitopes in AA.
获得性再生障碍性贫血(AA)是一种罕见疾病,其特征为全血细胞减少和骨髓细胞减少。尽管实验和临床数据表明AA是一种T细胞介导的疾病,但迄今为止,免疫反应和激发抗原的性质均未明确。通过PCR技术在总淋巴细胞群体中鉴定受限的T细胞库支持抗原驱动的T细胞反应。为了研究克隆组成,我们在单细胞水平分析了T细胞受体(TCR)可变β链(Vβ)的基因重排。
从8例AA患者及健康对照的外周血和骨髓样本中显微操作分离CD3(+) T淋巴细胞。随后对扩增的TCRVβ链VDJ基因片段进行功能重排分析。对500多个功能重排的TCR基因座研究Vβ/Jβ基因片段的使用情况以及互补决定区3(CDR3)的分子组成。
与健康对照相比,Vβ序列证实AA患者在单细胞水平存在高度受限的T细胞库。在骨髓和外周血中均观察到Vβ13和Jβ2S7占优势。此外,在大多数患者中发现了个体克隆性T细胞扩增。然而,推导的CDR3氨基酸序列显示高度变异性,8例患者之间无共同基序。
分析的患者中存在个体克隆性T细胞扩增且抗原结合位点具有高度多样性,这表明AA中主要是个体化的激发表位。