Abe J, Kotzin B L, Meissner C, Melish M E, Takahashi M, Fulton D, Romagne F, Malissen B, Leung D Y
Department of Pediatrics, National Jewish Center for Immunology and Respiratory Medicine, Denver, Colorado 80206.
J Exp Med. 1993 Mar 1;177(3):791-6. doi: 10.1084/jem.177.3.791.
Kawasaki disease (KD) is an acute multisystem vasculitis of unknown etiology that is associated with marked activation of T cells and monocyte/macrophages. Using a quantitative polymerase chain reaction (PCR) technique, we recently found that the acute phase of KD is associated with the expansion of T cells expressing the V beta 2 and V beta 8.1 gene segments. In the present work, we used a newly developed anti-V beta 2 monoclonal antibody (mAb) and studied a new group of KD patients to extend our previous PCR results. Immunofluorescence analysis confirmed that V beta 2-bearing T cells are selectively increased in patients with acute KD. The increase occurred primarily in the CD4 T cell subset. The percentages of V beta 2+ T cells as determined by mAb reactivity and flow cytometry correlated linearly with V beta expression as quantitated by PCR. However, T cells from acute KD patients appeared to express proportionately higher levels of V beta 2 transcripts per cell as compared with healthy controls or convalescent KD patients. Sequence analysis of T cell receptor beta chain genes of V beta 2 and V beta 8.1 expressing T cells from acute KD patients showed extensive junctional region diversity. These data showing polyclonal expansion of V beta 2+ and V beta 8+ T cells in acute KD provide additional insight into the immunopathogenesis of this disease.
川崎病(KD)是一种病因不明的急性多系统血管炎,与T细胞及单核细胞/巨噬细胞的显著激活有关。我们最近利用定量聚合酶链反应(PCR)技术发现,KD急性期与表达Vβ2和Vβ8.1基因片段的T细胞扩增有关。在本研究中,我们使用新开发的抗Vβ2单克隆抗体(mAb),并对一组新的KD患者进行研究,以拓展我们之前的PCR结果。免疫荧光分析证实,急性KD患者中携带Vβ2的T细胞选择性增加。这种增加主要发生在CD4 T细胞亚群中。通过mAb反应性和流式细胞术测定的Vβ2+ T细胞百分比与通过PCR定量的Vβ表达呈线性相关。然而,与健康对照或KD恢复期患者相比,急性KD患者的T细胞似乎每个细胞表达的Vβ2转录本水平相对更高。对急性KD患者中表达Vβ2和Vβ8.1的T细胞的T细胞受体β链基因进行序列分析,结果显示连接区存在广泛的多样性。这些数据表明急性KD中Vβ2+和Vβ8+ T细胞的多克隆扩增,为该疾病的免疫发病机制提供了更多见解。