可溶性肿瘤坏死因子(sTNF)受体:骨髓移植相关并发症的可能预后标志物

Cytokines and molecular therapy Pub Date : 1996-12-01
R Or, A Kalinkovich, A Nagler, Z Weisman, E Naparstek, L Weiss, T Hahn
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引用次数: 0

摘要

肿瘤坏死因子(TNF)参与骨髓移植(BMT)相关并发症已被证实。对TNF的生物反应需要与特定细胞膜受体相互作用。这些受体的细胞外结构域作为可溶性分子释放到体液中,并参与TNF的生物活性。测定34例不同疾病行BMT患者血清p55和p75可溶性肿瘤坏死因子受体(sTNFR)水平。从移植前10天开始并持续到移植后110天的序贯研究显示,在随后出现主要移植相关并发症(TRC)的患者中,p55和p75 sTNFR水平显著升高。此外,在晚期发生严重TRC的患者,在bmt后发热期,两种sTNFR水平均比对照组增加2- 3倍。这些结果表明,血清sTNFR水平可作为BMT主要TRC的预后指标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Soluble tumor necrosis factor (sTNF) receptors: a possible prognostic marker for bone marrow transplantation-related complications.

Involvement of tumor necrosis factor (TNF) in bone marrow transplantation (BMT)-associated complications has been documented. Biological response to TNF requires interaction with specific cell membrane receptors. Extracellular domains of these receptors are released into body fluids as soluble molecules, and participate in the bioactivity of TNF. Serum levels of p55 and p75 soluble tumor necrosis factor receptors (sTNFR) were determined in 34 patients with different diseases who underwent BMT. Sequential studies initiated 10 days before BMT and continued up to 110 days post-transplantation showed that p55 and p75 sTNFR levels were elevated significantly in patients who subsequently developed major transplant-related complications (TRC). Moreover, both sTNFR levels were increased 2- to 3-fold over control values during post-BMT febrile periods in those patients who at a later stage suffered major TRC. These results indicate that the serum level of sTNFR may be used as a prognostic marker for major TRC in BMT.

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