Hussein Mahmoud-Rezk A, Al-Assiri Mana, Musalam Adel O
Departments of Pathology and Urology, Assir Central Hospital and King Khalid University, Abha, Saudi Arabia.
Exp Mol Pathol. 2009 Apr;86(2):108-13. doi: 10.1016/j.yexmp.2008.11.010. Epub 2008 Dec 10.
Immune cell infiltrate is a constant feature in normal prostate, benign nodular prostatic hyperplasia and prostatic adenocarcinoma. This study elaborates on the cells of the immune system present in normal prostate, benign nodular prostatic hyperplasia and prostatic adenocarcinoma.
Here, we hypothesized that "the development of benign nodular prostatic hyperplasia and prostatic adenocarcinoma is associated with numeric alterations of the immune cell infiltrate".
A total of 50 transurethral prostatic resection specimens, each entailing normal prostate, benign nodular prostatic hyperplasia and high grade prostatic adenocarcinoma were evaluated for the density and phenotype of the immune cells using immunohistological methods and mouse monoclonal antibodies decorating T cells (CD3), histiocytes (CD68) and B lymphocytes (CD20).
Immune cell infiltrate was composed of T cells, histiocytes and B-lymphocytes. CD(+)3 T lymphocytes and CD68(+) cells were the predominant cell populations. We observed variations in the density of the immune cells among the normal prostate, benign nodular prostatic hyperplasia and high grade prostatic adenocarcinoma. Compared with normal prostate, benign nodular prostatic hyperplasia had a statistically significant high density of immune cells (3.4+/-0.4versus 13.5+/-1.0, P<0.00). In contrast, a significant decrease in the counts of these cells was observed in high-grade prostatic adenocarcinoma compared to benign nodular prostatic hyperplasia (13.5+/-1.0 versus 5.2+/-0.3, P<0.01).
The increased density of immune cells (predominantly CD(+)3 T cells) in benign nodular prostatic hyperplasia suggests that the initial response to cellular damage is mediated by cell-mediated immunity. The decreased density of immune cells in high-grade prostatic adenocarcinoma may reflect immunosuppression. The underlying mechanisms of these numeric variations are open for further investigations.
免疫细胞浸润是正常前列腺、良性前列腺结节增生和前列腺腺癌中的一个常见特征。本研究阐述了正常前列腺、良性前列腺结节增生和前列腺腺癌中存在的免疫系统细胞。
在此,我们假设“良性前列腺结节增生和前列腺腺癌的发生与免疫细胞浸润的数量改变有关”。
总共50份经尿道前列腺切除标本,每份标本包含正常前列腺、良性前列腺结节增生和高级别前列腺腺癌,使用免疫组织学方法和标记T细胞(CD3)、组织细胞(CD68)和B淋巴细胞(CD20)的小鼠单克隆抗体对免疫细胞的密度和表型进行评估。
免疫细胞浸润由T细胞、组织细胞和B淋巴细胞组成。CD(+)3 T淋巴细胞和CD68(+)细胞是主要细胞群体。我们观察到正常前列腺、良性前列腺结节增生和高级别前列腺腺癌之间免疫细胞密度存在差异。与正常前列腺相比,良性前列腺结节增生的免疫细胞密度在统计学上显著更高(3.4±0.4对13.5±1.0,P<0.00)。相比之下,与良性前列腺结节增生相比,高级别前列腺腺癌中这些细胞的数量显著减少(13.5±1.0对5.2±0.3,P<0.01)。
良性前列腺结节增生中免疫细胞(主要是CD(+)3 T细胞)密度增加表明对细胞损伤的初始反应是由细胞介导的免疫介导的。高级别前列腺腺癌中免疫细胞密度降低可能反映了免疫抑制。这些数量变化的潜在机制有待进一步研究。