Brooks E G, Filipovich A H, Padgett J W, Mamlock R, Goldblum R M
University of Texas Medical Branch, Department of Pediatrics, Child Health Research Center, Galveston, TX 77555-0366, USA.
Blood. 1999 Jan 1;93(1):242-50.
Patients with Omenn's syndrome have a form of severe immune deficiency that is associated with pathological features of graft-versus-host disease, except for the lack of foreign engraftment. It has been hypothesized that the disease's unique clinical features are mediated by an expanded population of autologous self-reactive T cells of limited clonality. In the current study, an investigation of the T-cell receptor (TCR) repertoire was undertaken to identify defects in T-cell rearrangement and development. The TCR repertoire in this group of patients was exquisitely restricted in the number of different TCR clonotypes, and some of these clonotypes seemed to have similar recognition motifs in the antigen-binding region, indicating antigen-driven proliferation of T lymphocytes. The TCRs from some patients lacked N- or P-nucleotide insertions and used proximal variable and joining gene segments, suggesting abnormal intrathymic T-cell development. Finally, abnormal assembly of gene segments and truncated rearrangements within nonproductive alleles suggested abnormalities in TCR rearrangement mechanisms. Overall, the findings suggest that inefficient and/or abnormal generation of TCRs may be a consistent feature of this disease.
奥门氏综合征患者患有一种严重的免疫缺陷形式,该形式与移植物抗宿主病的病理特征相关,但不存在外来植入的情况。据推测,该疾病独特的临床特征是由克隆性有限的自体自身反应性T细胞群体扩增介导的。在当前研究中,对T细胞受体(TCR)库进行了调查,以确定T细胞重排和发育中的缺陷。这组患者的TCR库在不同TCR克隆型的数量上受到极其严格的限制,其中一些克隆型在抗原结合区域似乎具有相似的识别基序,表明T淋巴细胞是由抗原驱动增殖的。一些患者的TCR缺乏N或P核苷酸插入,并使用近端可变和连接基因片段,提示胸腺内T细胞发育异常。最后,基因片段的异常组装和非生产性等位基因内的截短重排提示TCR重排机制存在异常。总体而言,这些发现表明TCR生成效率低下和/或异常可能是该疾病的一个持续特征。