Ohno Satoshi, Inagawa Hiroyuki, Dhar Dipok Kumar, Fujii Toshiyuki, Ueda Shuhei, Tachibana Mitsuo, Ohno Yumiko, Suzuki Nobutaka, Inoue Masaki, Soma Gen-Ichiro, Nagasue Naofumi
Department of Complementary and Alternative Medicine, Kanazawa University, Graduate School of Medical Science, Ishikawa, Japan.
Anticancer Res. 2005 Jan-Feb;25(1B):463-70.
Exactly what role does tumor-derived Fas ligand (FasL) play in cancer: maintaining the immune privilege site or inducing a pro-inflammatory effect? One possible hypothesis is that tumor-associated macrophages (TAM) act as the mediator that enables apoptosis of anti-tumor immune cells without FasL-related inflammation. We have evaluated the tumor FasL expression and TAM along the tumor margin and/or in cancer stroma, and their impact on the infiltration of immune-competent cells into the tumor nest.
Tissue specimens from consecutive 84 advanced gastric carcinoma patients, who had undergone a curative resection, were evaluated for TAM (CD68+ cells), tumor FasL expression and immune status (CD8 + T cells).
A high number of TAM significantly correlated with lymph node metastasis, intestinal type tumor and FasL expression. Although TAM had a tendency for an inverse correlation with the number of CD8+ T cells within the tumor nest (nest CD8) (p=0.0592), there was no correlation between FasL expression and nest CD8 (p=0.2158). This inverse association was found to be stronger in cases with both FasL-positive and high TAM tumors than in others (p=0.0139). The combination parameter of FasL-positive and high TAM became an independent prognostic factor in Cox's multivariate analysis, along with the pT status, nest CD8 and tumor cell apoptosis.
We suggest that TAM works harmoniously with tumor-derived FasL and serves as a barrier against the infiltration of CD8+ T cells into the cancer nest.
肿瘤来源的Fas配体(FasL)在癌症中究竟起什么作用:维持免疫豁免部位还是诱导促炎效应?一种可能的假说是,肿瘤相关巨噬细胞(TAM)作为介质,在无FasL相关炎症的情况下促使抗肿瘤免疫细胞凋亡。我们评估了肿瘤边缘和/或癌基质中肿瘤FasL的表达及TAM,以及它们对免疫活性细胞浸润至肿瘤巢的影响。
对连续84例接受根治性切除的晚期胃癌患者的组织标本进行TAM(CD68+细胞)、肿瘤FasL表达及免疫状态(CD8+T细胞)评估。
大量TAM与淋巴结转移、肠型肿瘤及FasL表达显著相关。尽管TAM与肿瘤巢内CD8+T细胞数量(巢内CD8)呈负相关趋势(p=0.0592),但FasL表达与巢内CD8之间无相关性(p=0.2158)。在FasL阳性且TAM高的肿瘤病例中,这种负相关比其他病例更强(p=0.0139)。在Cox多因素分析中,FasL阳性和高TAM的联合参数与pT状态、巢内CD8及肿瘤细胞凋亡一起成为独立的预后因素。
我们认为TAM与肿瘤来源的FasL协同作用,成为阻碍CD8+T细胞浸润至癌巢的屏障。