Cell Processing Section, Department of Transfusion Medicine, Clinical Center, National Institutes of Health, Bethesda, Maryland, USA.
Vaccine Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, USA.
Cytotherapy. 2018 May;20(5):728-739. doi: 10.1016/j.jcyt.2018.03.001. Epub 2018 Apr 11.
Pooled AB serum is often used as a media supplement for cell culture but it has the potential to transmit infectious diseases. To avoid this risk, we used autologous plasma as a media supplement for manufacturing dendritic cells (DCs) for cancer immunotherapy. We noticed inconsistencies in the DCs and investigated their nature and cause.
Adenovirus human epidural growth factor receptor 2 (adHER2/neu) DCs for 21 patients were manufactured from autologous peripheral blood monocytes that were treated with granulocyte-macrophage colony-stimulating factor (GM-CSF) and interleukin (IL)-4 for 3 days, transduced with Ad5f35HER2ECTM and then treated with lipopolysaccharide and interferon (IFN)-γ for 1 day. The cells were cultured in RPMI-1640 supplemented with either 10% heat inactivated autologous or AB plasma.
Twenty-eight adHER2/neu DCs were manufactured for 21 patients using autologous plasma and 68 were manufactured for 20 of those patients using AB plasma. The expression of human epidural growth factor receptor 2 (HER2/neu) was less for DCs manufactured with autologous plasma (70.3 ± 33.3% versus 86.1 ± 22.8%; P <0.01). Manufacturing adHER2/neu DCs using monocytes from three healthy subjects and plasma from one patient with low HER2/neu expression (18%) resulted in low HER2/neu expression by all three DCs (13%, 16% and 23%). Analysis of the levels of 1322 proteins in eight plasma samples associated with low HER2/neu expression and in 12 associated with high HER2/neu expression revealed that the levels of 14 predicted HER2/neu transduction efficiency.
The manufacture of adHER2/neu DC using autologous plasma as a media supplement resulted in inconsistent HER2/neu expression. It is likely that variability in the levels of multiple proteins in autologous plasma contributed to low HER2/neu expression.
混合 AB 血清常用于细胞培养的培养基补充物,但它有传播传染病的潜在风险。为了避免这种风险,我们使用自体血浆作为培养基补充物来制造用于癌症免疫治疗的树突状细胞 (DC)。我们注意到 DC 存在不一致性,并对其性质和原因进行了研究。
从接受过粒细胞-巨噬细胞集落刺激因子 (GM-CSF) 和白细胞介素 (IL)-4 处理 3 天的自体外周血单核细胞中制造了 21 名患者的腺病毒人类表皮生长因子受体 2 (adHER2/neu) DC,用 Ad5f35HER2ECTM 转导,然后用脂多糖和干扰素 (IFN)-γ处理 1 天。这些细胞在补充有 10%热灭活自体或 AB 血浆的 RPMI-1640 中培养。
使用自体血浆为 21 名患者制造了 28 个 adHER2/neu DC,为其中 20 名患者使用 AB 血浆制造了 68 个 adHER2/neu DC。使用自体血浆制造的 DC 中人表皮生长因子受体 2 (HER2/neu) 的表达较低(70.3±33.3% 与 86.1±22.8%;P<0.01)。使用来自 3 名健康受试者的单核细胞和来自一名 HER2/neu 表达低(18%)的患者的血浆制造 adHER2/neu DC,导致所有 3 个 DC 的 HER2/neu 表达均较低(13%、16%和 23%)。对与低 HER2/neu 表达相关的 8 个血浆样本中的 1322 种蛋白质水平和与高 HER2/neu 表达相关的 12 个血浆样本中的蛋白质水平进行分析,发现 14 种预测 HER2/neu 转导效率的蛋白质水平。
使用自体血浆作为培养基补充物制造 adHER2/neu DC 会导致 HER2/neu 表达不一致。自体血浆中多种蛋白质水平的变化可能导致 HER2/neu 表达降低。