隔膜膜介导的免疫反应模拟危险信号:卵巢癌病例的初步研究

T. H. Chin, H. Peng, Cheng‐Tao Lin
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引用次数: 0

摘要

危险信号于1994年首次提出。面对危险信号,树突状细胞作为t细胞免疫系统的指挥者,会成熟起来,进一步增强t细胞的应答能力。透明质酸是一种内源性危险信号。由于Seprafilm(主要用于防止术后粘连)也是一种基于透明质酸的药物,因此我们选择Seprafilm作为增加t细胞反应的新兴危险信号的“候选”。我们在10例卵巢癌患者中进行了一项初步研究,比较使用Seprafilm(5例)和不使用Seprafilm(5例)的患者的免疫风险概况。我们发现两组之间的免疫风险概况没有统计学差异。然而,观察到Seprafilm组CD4升高的趋势,提示Seprafilm可能是一种可选药物模拟危险信号。Seprafilm增强宿主免疫监测提高肿瘤患者生存率的潜在价值尚不清楚,需要进一步研究以明确临床应用的可能性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Seprafilm Mediated Immune Response Mimic Danger Signal: A Pilot Studyin Ovarian Cancer Cases
Danger signal was first proposed in 1994. In response to danger signal, dendritic cells, as the director of the T-cell immune system, would be matured and further enhance T-cell response. Hyaluronan had been reported as one of endogenous danger signals. Because of Seprafilm (most used for preventing post-operation adhesion) is also an hyaluronate-based agent, so we choose Seprafilm as our “candidate” of emerging danger signal to increasing T-cell response. We perform a pilot study in 10 ovarian cancer patients to compare the immune risk profiles between cases using Seprafilm (5 cases) and not using Seprafilm (5 cases). We found that there is no statistical difference on the immune risk profiles between two groups. However, a trend of increased CD4 in Seprafilm group was noted, indicating that Seprafilm might be an optional agent mimic danger signal. The potential value of Seprafilm to augment host immunosurveillance to improve survival rate in cancer patients is unknown, further study is needed to clarify the possibility of clinical applications.
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