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急性移植物抗宿主病中功能性和形态学抑制性T细胞缺陷

Functional and morphological suppressor T cell deficit in acute GVHD.

作者信息

Di Padova F, Gratwohl A, Corneo M, Speck B

出版信息

Clin Exp Immunol. 1984 Dec;58(3):611-8.

Abstract

Bone marrow transplantation (BMT) is currently used to treat patients with severe haematological disorders. One of its major complications is acute graft versus host disease (aGVHD). In this report we show that, during the early stages of lymphoid cell repopulation, an excess of suppressor T cell activity and a deficit of helper T cell activity are easily demonstrated by functional studies in healthy BMT recipients. On the contrary, in patients with active signs of aGVHD, a loss of suppressor T cells, as assessed by coculturing recipient T cells with donor B cells in an in vitro pokeweed mitogen (PWM) dependent Ig secreting assay, is detected. The loss of suppressor T cells in these patients is revealed also by the analysis of peripheral blood lymphocytes with the OKT5 suppressor cytotoxic monoclonal antibody (MoAb) but not with the OKT8 suppressor cytotoxic MoAb. Our data demonstrate that in several BMT recipients, during active aGVHD, a suppressor T cell deficit can be demonstrated both functionally and phenotypically.

摘要

骨髓移植(BMT)目前用于治疗严重血液系统疾病患者。其主要并发症之一是急性移植物抗宿主病(aGVHD)。在本报告中,我们表明,在淋巴细胞重新填充的早期阶段,通过对健康骨髓移植受者的功能研究很容易证明抑制性T细胞活性过高和辅助性T细胞活性不足。相反,在有aGVHD活动迹象的患者中,通过在体外商陆有丝分裂原(PWM)依赖性Ig分泌试验中将受者T细胞与供体B细胞共培养评估,发现抑制性T细胞减少。用OKT5抑制性细胞毒性单克隆抗体(MoAb)分析外周血淋巴细胞也显示这些患者中抑制性T细胞减少,但用OKT8抑制性细胞毒性MoAb分析则未显示。我们的数据表明,在一些骨髓移植受者中,在活动性aGVHD期间,抑制性T细胞缺陷在功能和表型上都可以得到证明。

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