Suppr超能文献

患有慢性不明原因淋巴结病的同性恋男性中辅助性T细胞和抑制性T细胞群体的免疫调节亚群。

Immunoregulatory subsets of the T helper and T suppressor cell populations in homosexual men with chronic unexplained lymphadenopathy.

作者信息

Nicholson J K, McDougal J S, Spira T J, Cross G D, Jones B M, Reinherz E L

出版信息

J Clin Invest. 1984 Jan;73(1):191-201. doi: 10.1172/JCI111190.

Abstract

Unexplained, generalized lymphadenopathy in homosexual men, which can be a prodrome to the acquired immunodeficiency syndrome, is associated with impaired cell-mediated immunity, a low ratio of T helper-inducer to T suppressor-cytotoxic cells (defined by the T4 and T8 monoclonal antibodies), and hypergammaglobulinemia. We performed double-marker studies on T cells by using a panel of monoclonal antibodies (Ia, T17, TQ1, and Leu-8), which reportedly detect activation or functional subsets of the T4 and T8 T cell populations. The T4:TQ1- or T4:Leu-8- subset, which is the major helper subset for B cell responses, is normally represented in lymphadenopathy patients. A depression in the reciprocal subset, T4:TQ1+ or T4:Leu-8+, accounts for the T4 T cell defect. Similarly, the TQ1 and Leu-8 markers delineate the abnormality of T8 T cells: the T8:TQ1- or T8:Leu-8- subset is elevated, whereas the T8:TQ1+ or T8:Leu-8+ subset is normally represented. We found no evidence of excessive activation of T4 T cells by using the T17 or Ia monoclonal antibodies. We did find an overall increase in Ia-positive T cells; however, this was due to increased T8:Ia+ cells. In functional studies, immunoglobulin production induced by pokeweed was subnormal. Most lymphadenopathy patients had normal T helper cell function when combined with normal B cells. The dampened pokeweed responses could be partially explained by depression of the T4:TQ1+ (or T4:Leu-8+) subset (which has minor help-associated function) and/or greater than expected suppression. However, subnormal pokeweed responses could not be totally explained by immunoregulatory T cell abnormalities because we also found an intrinsic defect in the B cell responses of lymphadenopathy patients.

摘要

同性恋男性中出现的不明原因的全身性淋巴结病,可能是获得性免疫缺陷综合征的前驱症状,与细胞介导的免疫功能受损、辅助诱导性T细胞与抑制性细胞毒性T细胞的比例降低(由T4和T8单克隆抗体定义)以及高球蛋白血症有关。我们使用一组单克隆抗体(Ia、T17、TQ1和Leu-8)对T细胞进行了双标记研究,据报道这些抗体可检测T4和T8 T细胞群体的激活或功能亚群。T4:TQ1-或T4:Leu-8-亚群是B细胞反应的主要辅助亚群,在淋巴结病患者中通常存在。相互对应的亚群T4:TQ1+或T4:Leu-8+的减少导致了T4 T细胞缺陷。同样,TQ1和Leu-8标记描绘了T8 T细胞的异常:T8:TQ1-或T8:Leu-8-亚群升高,而T8:TQ1+或T8:Leu-8+亚群正常存在。我们使用T17或Ia单克隆抗体未发现T4 T细胞过度激活的证据。我们确实发现Ia阳性T细胞总体增加;然而,这是由于T8:Ia+细胞增加所致。在功能研究中,商陆诱导的免疫球蛋白产生低于正常水平。大多数淋巴结病患者在与正常B细胞结合时T辅助细胞功能正常。商陆反应减弱部分可由T4:TQ1+(或T4:Leu-8+)亚群的减少(其具有较小的辅助相关功能)和/或大于预期的抑制作用来解释。然而,商陆反应低于正常水平不能完全由免疫调节性T细胞异常来解释,因为我们还发现淋巴结病患者的B细胞反应存在内在缺陷。

相似文献

引用本文的文献

本文引用的文献

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验