Rodriguez Paulo C, Ernstoff Marc S, Hernandez Claudia, Atkins Michael, Zabaleta Jovanny, Sierra Rosa, Ochoa Augusto C
Department of Microbiology, Stanley S Scott Cancer Center, Louisiana State University Health Sciences Center, New Orleans, Louisiana 70112, USA.
Cancer Res. 2009 Feb 15;69(4):1553-60. doi: 10.1158/0008-5472.CAN-08-1921. Epub 2009 Feb 5.
Myeloid-derived suppressor cells (MDSC) producing arginase I are increased in the peripheral blood of patients with renal cell carcinoma (RCC). MDSC inhibit T-cell function by reducing the availability of L-arginine and are therefore considered an important tumor escape mechanism. We aimed to determine the origin of arginase I-producing MDSC in RCC patients and to identify the mechanisms used to deplete extracellular L-arginine. The results show that human MDSC are a subpopulation of activated polymorphonuclear (PMN) cells expressing high levels of CD66b, CD11b, and VEGFR1 and low levels of CD62L and CD16. In contrast to murine MDSC, human MDSC do not deplete L-arginine by increasing its uptake but instead release arginase I into the circulation. Activation of normal PMN induces phenotypic and functional changes similar to MDSC and also promotes the release of arginase I from intracellular granules. Interestingly, although activation of normal PMN usually ends with apoptosis, MDSC showed no increase in apoptosis compared with autologous PMN or PMN obtained from normal controls. High levels of VEGF have been shown to increase suppressor immature myeloid dendritic cells in cancer patients. Treatment of RCC patients with anti-VEGF antibody bevacizumab, however, did not reduce the accumulation of MDSC in peripheral blood. In contrast, the addition of interleukin-2 to the treatment increased the number of MDSC in peripheral blood and the plasma levels of arginase I. These results may provide new insights on the mechanisms of tumor-induced anergy/tolerance and may help explain why some immunotherapies fail to induce an antitumor response.
产生精氨酸酶I的髓系来源抑制细胞(MDSC)在肾细胞癌(RCC)患者的外周血中增多。MDSC通过降低L-精氨酸的可用性来抑制T细胞功能,因此被认为是一种重要的肿瘤逃逸机制。我们旨在确定RCC患者中产生精氨酸酶I的MDSC的来源,并确定用于消耗细胞外L-精氨酸的机制。结果表明,人MDSC是活化的多形核(PMN)细胞的一个亚群,表达高水平的CD66b、CD11b和VEGFR1,低水平的CD62L和CD16。与小鼠MDSC不同,人MDSC不会通过增加L-精氨酸的摄取来消耗它,而是将精氨酸酶I释放到循环中。正常PMN的激活会诱导类似于MDSC的表型和功能变化,也会促进精氨酸酶I从细胞内颗粒中释放。有趣的是,尽管正常PMN的激活通常以凋亡结束,但与自体PMN或从正常对照获得的PMN相比,MDSC的凋亡没有增加。高水平的VEGF已被证明会增加癌症患者中抑制性未成熟髓样树突状细胞。然而,用抗VEGF抗体贝伐单抗治疗RCC患者并没有减少外周血中MDSC的积累。相反,在治疗中添加白细胞介素-2会增加外周血中MDSC的数量和精氨酸酶I的血浆水平。这些结果可能为肿瘤诱导的无反应/耐受机制提供新的见解,并可能有助于解释为什么一些免疫疗法未能诱导抗肿瘤反应。