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甲状腺癌中的T淋巴细胞、CD68阳性细胞与血管生成

T lymphocytes, CD68-positive cells and vascularisation in thyroid carcinomas.

作者信息

Herrmann G, Schumm-Draeger P M, Müller C, Atai E, Wenzel B, Fabian T, Usadel K H, Hübner K

机构信息

Department of Pathology, J.W. Goethe University, Frankfurt am Main, Germany.

出版信息

J Cancer Res Clin Oncol. 1994;120(11):651-6. doi: 10.1007/BF01245376.

Abstract

Immunohistochemical detection and quantification of CD3- and CD45RO-positive lymphocytes and CD68-positive cells in 75 thyroid carcinomas of follicular cell origin revealed rising levels for these parameters associated with dedifferentiation. A parallel trend towards reduction of vascularisation, determined as CD31-positive blood vessels, with decreasing differentiation became evident, statistically only significant when well-differentiated follicular and anaplastic carcinomas were compared. Positive correlations could be demonstrated between the density of CD68-, CD3-, and CD45RO-positive cells as well as between the density of CD68-, and CD3-, and CD45RO-positive cells and vascularisation. These correlations were expected, as the interaction of CD68-positive cells and T lymphocytes results in the production of angiogenesis factors, ultimately leading to better vascularisation of the tumour. Nevertheless, the tumour cells themselves are variously capable of producing angiogenic substances. The obvious lack of positive correlation between the density of tumour-infiltrating cells determined in this study and vascularisation, despite reduced vascularisation in less differentiated tumours that contained increasing numbers of tumour-infiltrating cells, seems to be due to functional heterogeneity of morphologically similar tumours.

摘要

对75例滤泡细胞源性甲状腺癌中CD3和CD45RO阳性淋巴细胞以及CD68阳性细胞进行免疫组化检测和定量分析,结果显示这些参数水平的升高与去分化相关。随着分化程度降低,以CD31阳性血管确定的血管生成呈平行下降趋势,仅在比较高分化滤泡癌和未分化癌时,统计学上有显著意义。CD68、CD3和CD45RO阳性细胞密度之间以及CD68、CD3和CD45RO阳性细胞密度与血管生成之间存在正相关。这些相关性是预期的,因为CD68阳性细胞与T淋巴细胞的相互作用导致血管生成因子的产生,最终导致肿瘤血管生成更好。然而,肿瘤细胞本身也有不同程度的产生血管生成物质的能力。尽管在分化程度较低、肿瘤浸润细胞数量增加的肿瘤中血管生成减少,但本研究中确定的肿瘤浸润细胞密度与血管生成之间明显缺乏正相关,这似乎是由于形态相似的肿瘤存在功能异质性。

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