凝胶蛋白和MMP12在朗格汉斯细胞组织细胞增多症中的预后意义。

The Korean Journal of Hematology Pub Date : 2012-12-01 Epub Date: 2012-12-24 DOI:10.5045/kjh.2012.47.4.267
Jong-Jin Seo, Taeshik Cho, Sun-Young Kim, Ibrahim Nassour, Hee-Jin Kim, Yeon-Jung Lim, Kyung-Nam Koh, Ho-Joon Im
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引用次数: 6

摘要

背景:凝胶蛋白和基质金属蛋白酶12 (MMP12)在朗格汉斯细胞组织细胞增多症(LCH)中有表达,但其临床意义尚不清楚。我们研究了这些蛋白与LCH患者临床表现的关系。方法:回顾性分析1998年至2008年间诊断为LCH的患者的临床资料并进行随访。可用福尔马林固定、石蜡包埋的标本进行凝胶和MMP12免疫组化染色。我们分析了这些蛋白的表达水平及其与LCH临床特征的关系。结果:36例经CD1a阳性诊断为LCH且有临床表现的患者(男20例,女16例)可进行免疫组织化学染色。患者中位年龄为62个月(范围5至207个月)。凝胶蛋白的表达各不相同;高17例(47.2%),低11例(30.6%),无8例(22.2%)。gelsolin高表达组多脏器及危险脏器受累倾向较高,但无统计学意义。MMP12仅在7例(19.4%)患者中检测到,这些患者表现出多系统受累(P=0.018),与MMP12阴性染色的患者相比,无事件生存率(P=0.002)较低。结论:Gelsolin和MMP12的表达可能与LCH的临床病程有关,其中MMP12的表达与重度LCH的关系尤为密切。gelsolin和MMP12在LCH发病机制中的确切作用和意义需要在更大的人群中进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Prognostic significance of gelsolin and MMP12 in Langerhans cell histiocytosis.

Prognostic significance of gelsolin and MMP12 in Langerhans cell histiocytosis.

Prognostic significance of gelsolin and MMP12 in Langerhans cell histiocytosis.

Prognostic significance of gelsolin and MMP12 in Langerhans cell histiocytosis.

Background: Gelsolin and matrix metalloproteinase 12 (MMP12) expression has been reported in Langerhans cell histiocytosis (LCH), but the clinical significance of this expression is unknown. We investigated the associations of these proteins with clinical manifestations in patients diagnosed with LCH.

Methods: We performed a retrospective analysis of clinical data from patients diagnosed with LCH and followed up between 1998 and 2008. Available formalin-fixed, paraffin-embedded specimens were used for gelsolin and MMP12 immunohistochemical staining. We analyzed the expression levels of these proteins and their associations with LCH clinical features.

Results: Specimens from 36 patients (20 males, 16 females) with a diagnosis of LCH based on CD1a positivity with clinical manifestations were available for immunohistochemical staining. Median patient age was 62 months (range, 5 to 207). The expression of gelsolin varied; it was high in 17 patients (47.2%), low in 11 patients (30.6%), and absent in 8 patients (22.2%). The high gelsolin expression group had a higher tendency for multi-organ and risk organ involvement, although the trend was not statistically significant. MMP12 was detected only in 7 patients (19.4%) who showed multi-system involvement (P=0.018) and lower event-free survival (P=0.002) in comparison to patients with negative MMP12 staining.

Conclusion: Gelsolin and MMP12 expression may be associated with the clinical course of LCH, and MMP12 expression may be particularly associated with severe LCH. Further studies of larger populations are needed to define the precise role and significance of gelsolin and MMP12 in the pathogenesis of LCH.

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