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霍奇金病中由抑制性淋巴细胞和单核细胞介导的细胞介导免疫受损。

Impaired cell-mediated immunity in Hodgkin's disease mediated by suppressor lymphocytes and monocytes.

作者信息

Hillinger S M, Herzig G P

出版信息

J Clin Invest. 1978 Jun;61(6):1620-7. doi: 10.1172/JCI109082.

Abstract

In Hodgkin's disease a possible mechanism for impaired cellular immunity is cell-mediated suppression, defined as the inhibitory interaction between suppressor cells and effector lymphocytes. To test for the presence of suppressor cells in peripheral blood, we have modified the standard, one-way mixed lymphocyte culture by adding mitomycin C-treated mononuclear cells from the responder. Suppression, expressed as a percent of the base-line mixed lymphocyte culture in which these extra cells are not present, results in a reduction of thymidine incorporated in the modified culture (i.e., 100% suppression = no net thymidine incorporation; 0% suppression = identical thymidine incorporation in both the modified and baseline culture). Suppression was found to be significantly increased in patients with both active Hodgkin's disease (78+/-4.6%) and remission Hodgkin's disease (58+/-9.3%) compared to normal individuals (21+/-6.9%) (mean+/-SE). The degree and frequency of suppression were not influenced by disease stage or prior therapy. Cell purification techniques revealed (in 10 patients studied) the suppressor cell to be a monocyte in 6, and a thymus-derived lymphocyte in 4. Possible genetic restriction of the suppressor cell interaction was indicated by a failure of suppressor cells to alter the response of lymphocytes from unrelated individuals, but suppression was obtained with lymphocytes from a histocompatible sibling. Although mononuclear cells from normal individuals suppress less frequently than cells from patients with Hodgkin's disease, normals may demonstrate suppression comparable to that observed in Hodgkin's patients. This finding suggests that suppression is a normal immunoregulatory mechanism which is altered in Hodgkin's disease.

摘要

在霍奇金病中,细胞免疫受损的一种可能机制是细胞介导的抑制作用,即抑制细胞与效应淋巴细胞之间的抑制性相互作用。为了检测外周血中是否存在抑制细胞,我们对标准的单向混合淋巴细胞培养进行了改良,方法是加入经丝裂霉素C处理的来自反应者的单核细胞。抑制作用以不存在这些额外细胞时的基线混合淋巴细胞培养的百分比来表示,结果是改良培养中掺入的胸苷减少(即,100%抑制 = 无净胸苷掺入;0%抑制 = 改良培养和基线培养中的胸苷掺入相同)。与正常个体(21±6.9%)(均值±标准误)相比,发现活动性霍奇金病患者(78±4.6%)和缓解期霍奇金病患者(58±9.3%)的抑制作用显著增强。抑制的程度和频率不受疾病分期或既往治疗的影响。细胞纯化技术显示(在研究的10名患者中),6名患者的抑制细胞为单核细胞,4名患者的为胸腺来源的淋巴细胞。抑制细胞相互作用可能存在的遗传限制表现为,抑制细胞不能改变来自无关个体的淋巴细胞的反应,但来自组织相容性同胞的淋巴细胞则可产生抑制作用。尽管正常个体的单核细胞产生抑制作用的频率低于霍奇金病患者的细胞,但正常人也可能表现出与霍奇金病患者相当的抑制作用。这一发现表明,抑制作用是一种正常的免疫调节机制,在霍奇金病中发生了改变。

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Rosette-forming lymphocytes in Hodgkin's disease.霍奇金病中的玫瑰花结形成淋巴细胞。
N Engl J Med. 1973 Oct 18;289(16):863. doi: 10.1056/NEJM197310182891616.

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