Foss H D, Herbst H, Oelmann E, Samol J, Grebe M, Blankenstein T, Matthes J, Qin Z H, Falini B, Pileri S
Institute of Pathology, Klinikum Steglitz, Free University Berlin, Germany.
Br J Haematol. 1993 Aug;84(4):627-35. doi: 10.1111/j.1365-2141.1993.tb03138.x.
Tissue specimens from 26 cases of Hodgkin's disease (HD) and six HD-derived cell lines were analysed for tumour necrosis factor (TNF), lymphotoxin (LT), and interleukin (IL)-6 RNA transcripts by in situ hybridization, in some cases subsequent to immunohistology for CD30 antigen. LT and TNF transcripts were found in tumour cells of all cases; IL-6 gene transcripts were detectable in 19/23 cases. Presence of RNA specific for these cytokines was not correlated with any of the following parameters: sex, symptoms and histotype, as well as immunophenotype and association of the tumour cells with Epstein-Barr virus. Rather, the presence of LT, TNF and IL-6 transcripts appeared to characterize Hodgkin and Reed-Sternberg cells in general, supporting concepts which suggest that HD represents a malignancy of cytokine secreting activated cells, and that many of the features distinguishing HD from other malignant lymphomas may ultimately be due to expression of cytokines. LT and TNF RNA transcripts were also found in five HD-derived cell lines, whereas supernatants of these cell lines contained high levels of LT, but low or undetectable levels of TNF activity. This suggests that, although not detectable at the level of RNA transcripts, differences between HD cases may exist on the level of cytokine gene transcript processing, translation and polypeptide secretion.
通过原位杂交技术,对26例霍奇金淋巴瘤(HD)组织标本及6种HD来源的细胞系进行了肿瘤坏死因子(TNF)、淋巴毒素(LT)和白细胞介素(IL)-6 RNA转录本分析,部分病例在进行CD30抗原免疫组织化学检测之后进行。所有病例的肿瘤细胞中均发现LT和TNF转录本;23例中有19例可检测到IL-6基因转录本。这些细胞因子特异性RNA的存在与以下任何参数均无相关性:性别、症状和组织学类型,以及免疫表型和肿瘤细胞与爱泼斯坦-巴尔病毒的关联。相反,LT、TNF和IL-6转录本的存在似乎是霍奇金和里德-斯腾伯格细胞的一般特征,支持了以下观点:HD代表分泌细胞因子的活化细胞的恶性肿瘤,且HD与其他恶性淋巴瘤的许多区别特征可能最终归因于细胞因子的表达。在5种HD来源的细胞系中也发现了LT和TNF RNA转录本,而这些细胞系的上清液中含有高水平的LT,但TNF活性水平较低或无法检测到。这表明,尽管在RNA转录本水平上无法检测到,但HD病例之间在细胞因子基因转录本加工、翻译和多肽分泌水平上可能存在差异。