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一名用 HLA 不相合胎儿干细胞重建的重症联合免疫缺陷病患者作为研究移植耐受的模型。

A SCID patient reconstituted with HLA-incompatible fetal stem cells as a model for studying transplantation tolerance.

作者信息

Roncarolo M G, Bacchetta R, Bigler M, Touraine J L, de Vries J E, Spits H

机构信息

DNAX Research Institute, Human Immunology Department, Palo Alto, CA 94304-1104.

出版信息

Blood Cells. 1991;17(2):391-402.

PMID:1680508
Abstract

We studied a severe combined immunodeficiency (SCID) patient who received transplantations with completely HLA-mismatched fetal liver and thymus from two different donors. The patient is now 14 years old, healthy and shows normal immunoresponses to recall antigens. His T cells are of donor origin, whereas the monocytes, B cells, and natural killer (NK) cells are of the recipient. The successful immunological reconstitution raised questions as to how T and B cells could collaborate across an HLA barrier and how tolerance was achieved. We have shown that tetanus toxin-specific T cell clones isolated from this patient recognized this antigen in the context of host and not of donor HLA-DR, indicating that those cells were educated in the host environment, presumably the thymus. Despite this, an unexpectedly high frequency of host-reactive clones was found that could recognize MHC antigens of the host. It was particularly striking that CD8+ CTL clones were obtained that recognized class I MHC antigens on the host cells. Nevertheless, the patient did not show any sign of acute or chronic graft-versus-host disease (GVHD). These data indicated that no or only incomplete clonal deletion had taken place in this patient and suggest the presence of a peripheral suppressor mechanism. Thus far, we have no indication for the existence of suppressor T cells. Inasmuch as it was found that host-reactive T cells fail to produce IL-4, which is exceptional for CD4+ T cells, we are exploring the possibility that abnormal cytokine production patterns of host-reactive T cells are associated with suppression of these cells in vivo.

摘要

我们研究了一名重症联合免疫缺陷(SCID)患者,该患者接受了来自两名不同供体的完全HLA不匹配的胎儿肝脏和胸腺移植。患者现已14岁,身体健康,对回忆抗原表现出正常的免疫反应。他的T细胞来源于供体,而单核细胞、B细胞和自然杀伤(NK)细胞来源于受体。成功的免疫重建引发了关于T细胞和B细胞如何跨越HLA屏障协作以及如何实现耐受性的问题。我们已经表明,从该患者分离出的破伤风毒素特异性T细胞克隆在宿主而非供体HLA-DR的背景下识别该抗原,这表明这些细胞是在宿主环境中,大概是在胸腺中接受教育的。尽管如此,仍发现了意外高频率的可识别宿主MHC抗原的宿主反应性克隆。特别引人注目的是获得了能够识别宿主细胞上I类MHC抗原的CD8 + CTL克隆。然而,该患者没有表现出任何急性或慢性移植物抗宿主病(GVHD)的迹象。这些数据表明该患者未发生或仅发生了不完全的克隆清除,并提示存在外周抑制机制。到目前为止,我们没有迹象表明存在抑制性T细胞。由于发现宿主反应性T细胞不能产生IL-4,这对于CD4 + T细胞来说是异常的,我们正在探索宿主反应性T细胞异常的细胞因子产生模式是否与这些细胞在体内的抑制有关的可能性。

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