Freitag Lukas, von Kaisenberg Constantin, Kreipe Hans, Hussein Kais
Institute of Pathology, Hannover Medical School, Hannover, Germany.
Int J Clin Exp Pathol. 2013 May 15;6(6):1103-11. Print 2013.
Chronic histiocytic intervillositis of the placenta (CHI) is a rare and potentially recurrent disease. Characteristically it shows accumulation of CD68+ cells in the intervillous space but no destructive tissue infiltration. An immunopathological background is likely but it is unknown what attracts circulating monocytes to the placenta.
We analysed the expression profile of 102 inflammation- and angiogenesis-associated genes with real-time reverse transcriptase-polymerase chain reaction (RT-PCR) in 16 placentas: CHI (n = 5) and, as controls, villitis of unknown aetiology (VUE, n = 4) and normal placenta (n = 7).
Compared to controls, CHI had significantly higher levels of matrix metallopeptidase 9 (MMP9) and transforming growth factor, beta receptor 1 (TGFBR1). MMP14 was lower in VUE than CHI (p < 0.05) and controls (not significant). Chemokine (C-X-C motif) ligand 9 (CXCL9), CXCL12, chemokine (C-C motif) ligand 5 (CCL5) and TIMP metallopeptidase inhibitor 1 (TIMP1) were significantly higher in VUE versus controls but not deregulated in CHI. The expression profile could not clearly discriminate CHI from VUE or controls but a tendency for grouping of massive CHI was found. Angiogenesis-associated factors were not deregulated in CHI.
The discrepancy of massive histiocytic accumulation and the lack of striking up-regulation of cytokines might be the basis of the non-destructive behaviour of the histiocytes in CHI.
胎盘慢性组织细胞性绒毛间炎(CHI)是一种罕见且可能复发的疾病。其特征是绒毛间隙中CD68 +细胞积聚,但无破坏性组织浸润。可能存在免疫病理背景,但尚不清楚是什么吸引循环单核细胞至胎盘。
我们采用实时逆转录聚合酶链反应(RT-PCR)分析了16个胎盘(CHI,n = 5;作为对照,不明病因绒毛炎(VUE,n = 4)和正常胎盘(n = 7))中102个炎症和血管生成相关基因的表达谱。
与对照组相比,CHI中基质金属蛋白酶9(MMP9)和转化生长因子β受体1(TGFBR1)水平显著更高。VUE中MMP14低于CHI(p < 0.05)和对照组(无显著性差异)。趋化因子(C-X-C基序)配体9(CXCL9)、CXCL12、趋化因子(C-C基序)配体5(CCL5)和金属蛋白酶组织抑制因子1(TIMP1)在VUE中相对于对照组显著更高,但在CHI中未失调。该表达谱不能明确区分CHI与VUE或对照组,但发现大量CHI有分组趋势。血管生成相关因子在CHI中未失调。
大量组织细胞积聚与细胞因子缺乏显著上调之间的差异可能是CHI中组织细胞非破坏性行为的基础。