Vacca A, Ribatti D, Ruco L, Giacchetta F, Nico B, Quondamatteo F, Ria R, Iurlaro M, Dammacco F
Department of Biomedical Sciences and Human Oncology, University of Bari Medical School, Italy.
Br J Cancer. 1999 Feb;79(5-6):965-70. doi: 10.1038/sj.bjc.6690154.
Node biopsies of 30 benign lymphadenopathies and 71 B-cell non-Hodgkin's lymphomas (B-NHLs) were investigated for microvessel and macrophage counts using immunohistochemistry and morphometric analysis. Both counts were significantly higher in B-NHL. Moreover, when these were grouped into low-grade and high-grade lymphomas, according to the Kiel classification and Working Formulation (WF), statistically significant higher counts were found in the high-grade tumours. Immunohistochemistry and electron microscopy revealed a close spatial association between microvessels and macrophages. Overall, the results suggest that, in analogy to what has already been shown in solid tumours, angiogenesis occurring in B-NHLs increases with tumour progression, and that macrophages promote the induction of angiogenesis via the release of their angiogenic factors.
采用免疫组织化学和形态计量分析方法,对30例良性淋巴结病和71例B细胞非霍奇金淋巴瘤(B-NHL)的淋巴结活检组织进行微血管和巨噬细胞计数研究。B-NHL中的这两项计数均显著更高。此外,根据基尔分类法和工作分类法(WF)将这些淋巴瘤分为低度和高度淋巴瘤时,发现高度肿瘤中的计数在统计学上显著更高。免疫组织化学和电子显微镜检查显示微血管与巨噬细胞之间存在紧密的空间关联。总体而言,结果表明,与实体瘤中已显示的情况类似,B-NHL中发生的血管生成随肿瘤进展而增加,并且巨噬细胞通过释放其血管生成因子促进血管生成的诱导。