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一种缺乏CD3/Ti(WT31)复合体多克隆T细胞表面表达的体内功能性免疫系统。

An in vivo functional immune system lacking polyclonal T-cell surface expression of the CD3/Ti(WT31) complex.

作者信息

Regueiro J R, López-Botet M, De Landazuri M O, Alcami J, Corell A, Martín-Villa J M, Vicario J L, Arnaiz-Villena A

机构信息

Hospital Primero de Octubre, Madrid, Spain.

出版信息

Scand J Immunol. 1987 Dec;26(6):699-708. doi: 10.1111/j.1365-3083.1987.tb02306.x.

Abstract

A polyclonal T-cell receptor complex (TCR) expression defect (as detected with monoclonal antibody WT31) has been found in two children belonging to an otherwise healthy Spanish family. One of the sibs (V, who had been vaccinated with attenuated poliomyelitis virus) showed clinical signs of immunodeficiency with an autoimmune syndrome, but the other (older) sib (D, vaccinated with attenuated rubella, measles, mumps, and poliomyelitis viruses) has been symptomless throughout life. In contrast to both sibs' normal expression of other peripheral leucocyte markers, as measured by flow cytometry (including CD1, CD2, CD4, CD8, and CD16), only about 6% of CD2+ polyclonal T cells expressed surface antigen-specific T-cell receptor (Ti/WT31), and only about 23% weakly expressed surface CD3 determinants. On the remaining CD2+ T cells in each sib the expression of Ti and CD3 was undetectable; the defect in CD3 expression is very likely secondary to the defect in Ti expression. Natural killer (NK) activity was not increased in any of the sibs, ruling out a high content of NK cells among their CD2+ lymphocytes. Functional data indicate that CD3-mediated T-cell activation with anti-CD3 monoclonals and Ti-mediated responses to allogeneic and tetanus toxoid antigens were severely depressed, whereas activation via CD2 was normal in the T lymphocytes of both sibs. Genes encoding for Ti alpha, beta, and gamma chains did not show major alterations by southern blot analysis, and polyclonal beta chain genes rearrangements were detected in both children's T-cell blasts. Family clustering suggests a genetic pathogenesis, but linkage to HLA or other blood group markers has not been found. Sib V had a concomitant autoimmune disease and died after a severe autoimmune haemolytic anaemia, indicating a relationship between the TCR and generation of autoimmune clones. However, the resistance of both individuals to infection and to vaccination with attenuated viruses, and the fact that sib D has been symptomless to date questions the relative importance of the TCR in the immune response against infection, and suggests that alternative T-cell activation pathways and non-specific defence mechanisms (external surfaces--bound and/or cellular) may suffice under certain circumstances.

摘要

在一个原本健康的西班牙家庭的两名儿童中发现了多克隆T细胞受体复合物(TCR)表达缺陷(用单克隆抗体WT31检测)。其中一名同胞(V,曾接种减毒脊髓灰质炎病毒疫苗)表现出免疫缺陷伴自身免疫综合征的临床症状,但另一名(年长的)同胞(D,接种了减毒风疹、麻疹、腮腺炎和脊髓灰质炎病毒疫苗)一生都没有症状。与通过流式细胞术测量的两名同胞其他外周白细胞标志物的正常表达情况(包括CD1、CD2、CD4、CD8和CD16)不同,只有约6%的CD2+多克隆T细胞表达表面抗原特异性T细胞受体(Ti/WT31),只有约23%的细胞弱表达表面CD3决定簇。在每名同胞剩余的CD2+T细胞上,未检测到Ti和CD3的表达;CD3表达缺陷很可能继发于Ti表达缺陷。两名同胞的自然杀伤(NK)活性均未增加,排除了其CD2+淋巴细胞中NK细胞含量高的可能性。功能数据表明,用抗CD3单克隆抗体介导的CD3依赖性T细胞活化以及Ti介导的对同种异体和破伤风类毒素抗原的反应严重受损,而通过CD2介导的活化在两名同胞的T淋巴细胞中是正常的。通过Southern印迹分析,编码Tiα、β和γ链的基因未显示出主要改变,并且在两名儿童的T细胞母细胞中均检测到多克隆β链基因重排。家族聚集提示存在遗传发病机制,但未发现与HLA或其他血型标志物的连锁关系。同胞V患有伴发的自身免疫性疾病,在严重的自身免疫性溶血性贫血后死亡,表明TCR与自身免疫克隆的产生之间存在关联。然而,两人对感染和减毒病毒疫苗接种的抵抗力,以及同胞D至今无症状这一事实,对TCR在抗感染免疫反应中的相对重要性提出了质疑,并表明在某些情况下,替代性T细胞活化途径和非特异性防御机制(外表面结合和/或细胞性)可能就足够了。

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