Schwaab T, Weiss J E, Schned A R, Barth R J
Department of Surgery, Dartmouth Hitchcock Medical Center, Lebanon, New Hampshire 03756, USA.
J Immunother. 2001 Mar-Apr;24(2):130-7.
We quantitatively evaluated dendritic cell (DC) infiltration in primary colorectal cancers from 44 patients and metastatic colorectal tumors from 13 patients using immunohistochemistry for the DC marker CD83, HLA-DR, and the DC activation molecules CD40 and CD86. Nearly all CD83+ cells were also HLA-DR+, CD40+, and CD86+, indicating that the DCs that infiltrate colon cancer in vivo express the activation and costimulatory molecules associated with a mature DC phenotype. The density of DCs in colorectal cancer primaries was three times lower than that seen in normal colonic mucosa (0.29 versus 0.84 CD83+ cells/ high-power field (hpf), p < 0.001). Dendritic cells were rarely observed in metastatic tumors: DC density in metastases was sixfold lower than in colorectal primary tumors (0.05 versus 0.29 CD83+ cells/hpf, p < 0.001). Because cytokines have been shown, in vitro, to exert potent effects on DCs, we also evaluated the relationship between intratumor DC density and the expression of cytokines by tumor-infiltrating lymphocytes (TILs) and tumor cells. Expression of interleukin-10 and transforming growth factor beta by either TIL or tumor cells was not associated with decreased DC density or decreased expression of CD40 or CD86 on DCs. Tumor expression of vascular endothelial growth factor was associated with a more than twofold increase in DC density (p = 0.01). Patients who had a high proportion of TILs expressing tumor necrosis factor (TNF) had a greater intratumor mature DC density than patients with a low proportion of TNF + TIL (0.54 versus 0.21 CD83+ cells/hpf, p < 0.01).
我们运用免疫组织化学方法,检测树突状细胞(DC)标志物CD83、HLA-DR以及DC活化分子CD40和CD86,对44例原发性结直肠癌患者和13例转移性结直肠肿瘤患者进行了DC浸润的定量评估。几乎所有CD83+细胞同时也是HLA-DR+、CD40+和CD86+,这表明体内浸润结肠癌的DC表达与成熟DC表型相关的活化分子和共刺激分子。原发性结直肠癌中DC的密度比正常结肠黏膜低三倍(0.29对0.84个CD83+细胞/高倍视野(hpf),p<0.001)。在转移性肿瘤中很少观察到树突状细胞:转移灶中的DC密度比原发性结直肠癌低六倍(0.05对0.29个CD83+细胞/hpf,p<0.001)。由于细胞因子在体外已被证明对DC有显著作用,我们还评估了肿瘤内DC密度与肿瘤浸润淋巴细胞(TIL)和肿瘤细胞表达的细胞因子之间的关系。TIL或肿瘤细胞表达白细胞介素-10和转化生长因子β与DC密度降低或DC上CD40或CD86表达降低无关。肿瘤血管内皮生长因子的表达与DC密度增加两倍以上相关(p = 0.01)。肿瘤坏死因子(TNF)表达比例高的TIL患者,其肿瘤内成熟DC密度高于TNF+TIL比例低的患者(0.54对0.21个CD83+细胞/hpf,p<0.01)。