Ware R E, Howard T A
Department of Pediatrics, Duke University Medical Center, Durham, North Carolina 27710.
J Clin Immunol. 1994 Jul;14(4):237-47. doi: 10.1007/BF01552310.
Immune thrombocytopenic purpura (ITP) in childhood is a heterogeneous clinical disorder characterized by immune-mediated platelet destruction. Although generally considered to involve autoreactive B lymphocytes which produce antiplatelet antibodies, there is increasing evidence that T lymphocytes also play an important role in this autoimmune process. We studied 11 children with acute ITP and 19 children with chronic ITP and observed elevated numbers of TCR gamma delta+ T lymphocytes in several patients. In the three children with the highest elevations (TCR gamma delta+/CD3+ percentage ranging from 37.8 to 48.1% at initial evaluation), the expanded cell population exclusively expressed the surface V delta 2/V gamma 9 heterodimer and had enhanced in vitro proliferation to mycobacterial extracts and IL-2. Analysis of the nucleotide sequences used by these TCR gamma delta+ cells demonstrated a diverse set of VDDJC gene rearrangements, indicating polyclonal expansion of cells reminiscent of a superantigen response. There was a close correlation between the number of TCR gamma delta+ T lymphocytes and the degree of thrombocytopenia in each patient. TCR gamma delta+ T lymphocytes may be important in the pathogenesis of immune-mediated platelet destruction in some children with ITP.
儿童免疫性血小板减少性紫癜(ITP)是一种异质性临床疾病,其特征为免疫介导的血小板破坏。尽管通常认为该病涉及产生抗血小板抗体的自身反应性B淋巴细胞,但越来越多的证据表明,T淋巴细胞在这一自身免疫过程中也发挥着重要作用。我们研究了11例急性ITP患儿和19例慢性ITP患儿,观察到部分患者的TCRγδ+ T淋巴细胞数量增加。在3例升高幅度最大的患儿中(初始评估时TCRγδ+/CD3+百分比范围为37.8%至48.1%),扩增的细胞群体仅表达表面Vδ2/Vγ9异二聚体,并且对分枝杆菌提取物和IL-2的体外增殖增强。对这些TCRγδ+细胞使用的核苷酸序列分析显示出多种VDDJC基因重排,表明细胞的多克隆扩增类似于超抗原反应。每位患者的TCRγδ+ T淋巴细胞数量与血小板减少程度密切相关。TCRγδ+ T淋巴细胞可能在部分ITP患儿免疫介导的血小板破坏发病机制中起重要作用。