Seo Jong-Jin, Cho Taeshik, Kim Sun-Young, Nassour Ibrahim, Kim Hee-Jin, Lim Yeon-Jung, Koh Kyung-Nam, Im Ho-Joon
Division of Pediatric Hematology/Oncology, Department of Pediatrics, University of Ulsan College of Medicine & Asan Medical Center, Seoul, Korea.
Korean J Hematol. 2012 Dec;47(4):267-72. doi: 10.5045/kjh.2012.47.4.267. Epub 2012 Dec 24.
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.
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.
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.
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.
已有报道称凝溶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)中表达,但这种表达的临床意义尚不清楚。我们研究了这些蛋白与LCH诊断患者临床表现之间的关联。
我们对1998年至2008年期间诊断为LCH并接受随访的患者的临床资料进行了回顾性分析。使用现有的福尔马林固定、石蜡包埋标本进行凝溶胶蛋白和MMP12免疫组织化学染色。我们分析了这些蛋白的表达水平及其与LCH临床特征的关联。
36例(20例男性,16例女性)基于CD1a阳性且有临床表现而诊断为LCH的患者标本可用于免疫组织化学染色。患者中位年龄为62个月(范围5至207个月)。凝溶胶蛋白的表达各不相同;17例患者(47.2%)表达高,11例患者(30.6%)表达低,8例患者(22.2%)无表达。凝溶胶蛋白高表达组多器官和危险器官受累的倾向更高,尽管该趋势无统计学意义。与MMP12染色阴性的患者相比,仅在7例(19.4%)表现为多系统受累的患者中检测到MMP12(P=0.018),且其无事件生存期较低(P=0.002)。
凝溶胶蛋白和MMP12的表达可能与LCH的临床病程相关,且MMP12的表达可能尤其与严重LCH相关。需要对更多人群进行进一步研究,以明确凝溶胶蛋白和MMP12在LCH发病机制中的精确作用和意义。