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CD86表达对慢性淋巴细胞白血病细胞增殖和存活的影响。

The Effect of CD86 Expression on the Proliferation and the Survival of CLL Cells.

作者信息

Takács Ferenc, Tolnai-Kriston Csilla, Hernádfői Márk, Szabó Orsolya, Szalóki Gábor, Szepesi Ágota, Czeti Ágnes, Matolcsy András, Barna Gábor

机构信息

1st Department of Pathology and Experimental Cancer Research, Semmelweis University, Üllői út 26, Budapest, H-1085, Hungary.

出版信息

Pathol Oncol Res. 2019 Apr;25(2):647-652. doi: 10.1007/s12253-018-0512-7. Epub 2018 Nov 8.

Abstract

Micro-environment plays important role in the pathogenesis of CLL by providing protective niche for CLL cells. Several molecules play important role in communication between CLL cells and immune cells like CD86.Some of the data suggest that CLL patients with high CD86 level need earlier treatments and cells with higher CD86 expression has higher proliferation rate but the role of CD86 in the survival and proliferation of CLL cells is unclear. We investigated the effect of CD86 expression to CLL cells in 50 peripheral blood and 15 lymph node biopsy samples from CLL patients. Our results showed that the expressions of CD86 increased significantly after 7 day culturing in medium, or in the presence of bone marrow stromal cells (BMSCs). We found positive correlation between CD86 and CD23 expression (p < 0.05), but no correlation with other markers. Furthermore, no correlation were found between the CD86 expression and the proliferation of CLL cells. Analysis of clinical data showed that cases with high CD86 expression had lower level of serum lymphocyte count (p < 0.04) at the time of the diagnosis. CD86 shows multiple appearances in the lymph nodes containing pseudofollicules, but no correlation was found between CD86 positivity, and Ki67 positivity. Our results suggest that the use of CD86 molecule as a proliferation marker for CLL is highly questionable. However, the CD86 molecule may interfere with the immune system of patients with CLL by activating and depleting immune functions. That can be the reason why CD86 positivity may mean worse prognosis.

摘要

微环境通过为慢性淋巴细胞白血病(CLL)细胞提供保护性微环境,在CLL的发病机制中发挥重要作用。几种分子在CLL细胞与免疫细胞(如CD86)之间的通讯中起重要作用。一些数据表明,CD86水平高的CLL患者需要更早进行治疗,且CD86表达较高的细胞具有更高的增殖率,但CD86在CLL细胞存活和增殖中的作用尚不清楚。我们研究了CD86表达对50例CLL患者外周血和15例淋巴结活检样本中CLL细胞的影响。我们的结果显示,在培养基中或存在骨髓基质细胞(BMSC)的情况下培养7天后,CD86的表达显著增加。我们发现CD86与CD23表达之间呈正相关(p < 0.05),但与其他标志物无相关性。此外,未发现CD86表达与CLL细胞增殖之间存在相关性。临床数据分析表明,CD86高表达的病例在诊断时血清淋巴细胞计数水平较低(p < 0.04)。CD86在含有假滤泡的淋巴结中有多种表现形式,但未发现CD86阳性与Ki67阳性之间存在相关性。我们的结果表明,将CD86分子用作CLL的增殖标志物极具疑问。然而,CD86分子可能通过激活和消耗免疫功能来干扰CLL患者的免疫系统。这可能就是CD86阳性可能意味着预后较差的原因。

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