Garrity T, Pandit R, Wright M A, Benefield J, Keni S, Young M R
Department of Otolaryngology, Loyola University Stritch School of Medicine, Maywood, IL, USA.
Int J Cancer. 1997 Nov 27;73(5):663-9. doi: 10.1002/(sici)1097-0215(19971127)73:5<663::aid-ijc9>3.0.co;2-v.
Patients with head and neck squamous cell carcinoma (HNSCC) have profound immune deficiencies. In 65% of these patients, there is an increased intra-tumoral presence of immune-suppressive CD34+ progenitor cells. The goal of the present study was to determine whether CD34+ cell levels were also increased in the peripheral blood of HNSCC patients and if these immune-suppressive cells could be differentiated into dendritic cells. Our results showed that CD34+ cell levels are increased in the peripheral blood of HNSCC patients. To assess if these CD34+ cells could differentiate into dendritic cells, they were isolated from the blood of HNSCC patients and cultured for 12 days with various cytokine combinations. Culturing CD34+ cells with stem cell factor (c-kit ligand) plus granulocyte-macrophage colony-stimulating factor resulted in the appearance of a significant proportion of cells expressing phenotypic markers characteristic of dendritic cells. Also, including tumor necrosis factor-alpha yielded a significant proportion of cells resembling the bipotential precursor cells for dendritic cells and monocytes (CD14+CD1a+), in addition to the dendritic-like cells. When the differentiation inducer 1alpha,25-dihydroxyvitamin D3 [1,25(OH)2D3] was added along with the cytokine combinations, the yield of cells having characteristics of dendritic cells was further increased. Cells that were derived from CD34+ cell cultures containing 1,25(OH)2D3 had a more potent capacity to present the recall antigen tetanus toxoid to autologous peripheral blood leukocytes and to stimulate a mixed leukocyte response compared to cultures to which 1,25(OH)2D3 had not been added. Our results show that CD34+ cells, whose frequency is increased in HNSCC patients, can be differentiated into cells that phenotypically and functionally resemble dendritic cells and that 1,25(OH)2D3 accentuates this differentiation.
头颈部鳞状细胞癌(HNSCC)患者存在严重的免疫缺陷。在这些患者中,65%的患者肿瘤内免疫抑制性CD34+祖细胞的数量增加。本研究的目的是确定HNSCC患者外周血中CD34+细胞水平是否也升高,以及这些免疫抑制细胞是否可分化为树突状细胞。我们的结果表明,HNSCC患者外周血中CD34+细胞水平升高。为了评估这些CD34+细胞是否能分化为树突状细胞,从HNSCC患者血液中分离出这些细胞,并与各种细胞因子组合培养12天。用干细胞因子(c-kit配体)加粒细胞-巨噬细胞集落刺激因子培养CD34+细胞,导致出现大量表达树突状细胞特征性表型标志物的细胞。此外,加入肿瘤坏死因子-α后,除了树突状样细胞外,还产生了大量类似于树突状细胞和单核细胞双潜能前体细胞(CD14+CD1a+)的细胞。当与细胞因子组合一起加入分化诱导剂1α,25-二羟基维生素D3 [1,25(OH)2D3]时,具有树突状细胞特征的细胞产量进一步增加。与未添加1,25(OH)2D3的培养物相比,来自含有1,25(OH)2D3的CD34+细胞培养物的细胞向自体外周血白细胞呈递回忆抗原破伤风类毒素以及刺激混合淋巴细胞反应的能力更强。我们的结果表明,HNSCC患者中频率增加的CD34+细胞可分化为表型和功能上类似于树突状细胞的细胞,并且1,25(OH)2D3可增强这种分化。