The natural killer activity (cytotoxicity) of lymphocytes.

Annales immunologiae Hungaricae Pub Date : 1979-01-01
G G Petrányi, M Benczur, M Varga, G Györffy, E Gyódi, K Onody, R S Hollán
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Abstract

The authors' own investigations into the spontaneous lymphocyte-mediated cytotoxicity (SLMC) have been reviewed and discussed in th light of literary data. It is suggested that SLMC is a resultant of complex effects contributed by antibodies present in the human serum and those attached to the surface of lymphocytes as well as by spontaneous (sui generis) functions of effector cells. The lymphocytes eliciting SLMC belong to the "O" subpopulation, bear Fc receptors and are presumably, identical with "K" lymphocytes. In animal experiments, the authors have shown that the SLMC reaction directed againt a virus-induced tumour is under polygenetic control primarily governed by gene(s0 linked to the histocompatibility region. In man, similarly as in the mouse, SLMC was found to be a genetically-controlled lymphocyte function in which gene(s) linked to the HLA-A2 B12 or the HLA-A3 B7 haplotype may play a determining role. The authors' clinical observations indicate that LSMC represents an important part of the defense mechanism against malignancies and autoimmune diseases. Estimation and follow-up of SLMC may be useful in monitoring the clinical course.

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淋巴细胞的自然杀伤活性(细胞毒性)。
作者自己对自发性淋巴细胞介导的细胞毒性(SLMC)的研究已经根据文献资料进行了回顾和讨论。这表明,SLMC是存在于人血清中的抗体和附着在淋巴细胞表面的抗体以及效应细胞自发(自生)功能共同作用的结果。引发SLMC的淋巴细胞属于“O”亚群,携带Fc受体,可能与“K”淋巴细胞相同。在动物实验中,作者已经证明针对病毒诱导肿瘤的SLMC反应受多基因控制,主要由与组织相容性区相关的基因(50)控制。在人类中,与小鼠相似,SLMC被发现是一种遗传控制的淋巴细胞功能,其中与HLA-A2 B12或HLA-A3 B7单倍型相关的基因可能起决定性作用。作者的临床观察表明,LSMC是抵抗恶性肿瘤和自身免疫性疾病的防御机制的重要组成部分。SLMC的评估和随访可能有助于监测临床病程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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Immunodiffusion study on group-specific antigen of MC-29 chicken hepatoma. Studies of pre- and postimmunization antibodies of sheep. Synthesis and studies of transferrin. Potency of PPD preparations derived from M. tuberculosis and M. bovis. Immune responsiveness of patients with autoimmune diseases and immunodeficiency.
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