Hasselblom Sverker, Hansson Ulrika, Sigurdardottir Margret, Nilsson-Ehle Herman, Ridell Börje, Andersson Per-Ola
Section of Haematology and Coagulation, Department of Internal Medicine, Sahlgrenska University Hospital, Göteborg, Sweden.
Pathol Int. 2008 Aug;58(8):529-32. doi: 10.1111/j.1440-1827.2008.02268.x.
Tumor-associated macrophages (TAM) have been ascribed both pro- and anti-tumor properties, but the majority of clinical cancer studies have shown that the presence of a high number of TAM is related to poor prognosis, suggesting that TAM predominantly exert pro-tumoral activity. The prognostic role of TAM in patients with diffuse large B-cell lymphoma (DLBCL), however, is so far unknown. Therefore, TAM were immunohistochemically stained with a CD68 antibody in a retrospective, population-based study including 176 DLBCL patients treated with curative intent. With the exception that patients >60 years of age had a larger number of CD68+ cells (1143 vs 1018 cells/mm2; P = 0.05), no significant differences were found between the number of CD68+ cells and other clinical factors. Similarly, germinal center B-cell (GCB)/non-GCB immunophenotype or low/high Ki-67 percentage were not associated with CD68 expression. Finally, no significant correlation was found between the number of CD68+ cells and progression-free survival (P = 0.34) or overall survival (P = 0.94). These data indicate that the pro-tumor effect of TAM has limited clinical relevance in DLBCL patients, which could imply that therapeutic strategies aimed at enhancing their anti-tumor activity are of continuous clinical interest.
肿瘤相关巨噬细胞(TAM)具有促肿瘤和抗肿瘤两种特性,但大多数临床癌症研究表明,大量TAM的存在与预后不良有关,这表明TAM主要发挥促肿瘤活性。然而,TAM在弥漫性大B细胞淋巴瘤(DLBCL)患者中的预后作用目前尚不清楚。因此,在一项基于人群的回顾性研究中,对176例接受根治性治疗的DLBCL患者的TAM进行了CD68抗体免疫组化染色。除了60岁以上的患者有更多的CD68+细胞(1143个对1018个细胞/mm2;P = 0.05)外,CD68+细胞数量与其他临床因素之间未发现显著差异。同样,生发中心B细胞(GCB)/非GCB免疫表型或低/高Ki-67百分比与CD68表达无关。最后,CD68+细胞数量与无进展生存期(P = 0.34)或总生存期(P = 0.94)之间未发现显著相关性。这些数据表明,TAM的促肿瘤作用在DLBCL患者中的临床相关性有限,这可能意味着旨在增强其抗肿瘤活性的治疗策略仍具有持续的临床意义。