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卵巢癌患者腹水中单核细胞的表型及抗肿瘤活性

Phenotype and antitumor activity of ascitic fluid monocytes in patients with ovarian carcinoma.

作者信息

Melichar B, Savary C A, Patenia R, Templin S, Melicharova K, Freedman R S

机构信息

Departments of Gynecologic Oncology and Surgical Oncology, The University of Texas, M.D. Anderson Cancer Center, Houston, Texas.

出版信息

Int J Gynecol Cancer. 2003 Jul-Aug;13(4):435-43. doi: 10.1046/j.1525-1438.2003.13331.x.

Abstract

Monocytes/macrophages (MO/MA) represent a major leukocyte population in the peritoneal cavity of patients with epithelial ovarian cancer (EOC). We examined the phenotypic characteristics and antitumor cell activity of ascitic MO in patients with EOC. MO/MA phenotype was compared with MO in peripheral blood by two- and three-color flow cytometry. Cytotoxic/cytostatic effects of different cytokines on cultured EOC cells were measured by initial labeling or uptake inhibition of [methyl-3H] thymidine. Malignant ascites had higher proportion of MO/MA with the CD14brightCD16+ phenotype than peripheral blood. Cell surface antigen expression of activation and differentiation in peripheral blood and ascites, including CD38, CD40, CD64, and CD86, was higher on CD14brightCD16- and CD14brightCD16+ than on CD14dimCD16- cells. HLA-DR expression was higher on ascitic MO/MA than peripheral blood MO. Significant cytotoxic/cytostatic activity was elicited by treating ascitic MO/MA with interferon-gamma (IFN-gamma) and interleukin-2 (IL-2), but not with interleukin-12, paclitaxel, granulocyte-monocyte colony-stimulating factor (GM-CSF), or tumor necrosis factor-alpha (TNF-alpha). Soluble CD40Lt did not enhance MO/MA cytotoxic activity, and inhibited IFN-gamma or IL-2 induced cytoxicity. We conclude that MO/MA from ascites have elevated proportions of CD14brightCD16+ cells, showing phenotypic features of activation. IFN-gamma induces the cytotoxic and cytostatic activity of MO/MA that is inhibited by CD40Lt.

摘要

单核细胞/巨噬细胞(MO/MA)是上皮性卵巢癌(EOC)患者腹腔内主要的白细胞群体。我们检测了EOC患者腹水中MO的表型特征和抗肿瘤细胞活性。通过双色和三色流式细胞术将MO/MA表型与外周血中的MO进行比较。通过[甲基-3H]胸苷的初始标记或摄取抑制来测量不同细胞因子对培养的EOC细胞的细胞毒性/细胞生长抑制作用。恶性腹水中具有CD14brightCD16+表型的MO/MA比例高于外周血。外周血和腹水中包括CD38、CD40、CD64和CD86在内的激活和分化细胞表面抗原表达在CD14brightCD16-和CD14brightCD16+细胞上高于CD14dimCD16-细胞。腹水中的MO/MA上HLA-DR表达高于外周血中的MO。用干扰素-γ(IFN-γ)和白细胞介素-2(IL-2)处理腹水中的MO/MA可引发显著的细胞毒性/细胞生长抑制活性,但用白细胞介素-12、紫杉醇、粒细胞-单核细胞集落刺激因子(GM-CSF)或肿瘤坏死因子-α(TNF-α)处理则无此活性。可溶性CD40Lt不能增强MO/MA的细胞毒性活性,反而抑制IFN-γ或IL-2诱导的细胞毒性。我们得出结论,腹水中的MO/MA中CD14brightCD16+细胞比例升高,表现出激活的表型特征。IFN-γ诱导MO/MA的细胞毒性和细胞生长抑制活性,而这种活性受到CD40Lt的抑制。

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