Plasma IFN-γ and IL-6 levels correlate with peripheral T-cell numbers but not toxicity in RCC patients treated with CAR T-cells

被引:7
作者
Klaver, Yarne [1 ]
van Steenbergen, Sabine C. L. [1 ]
Sleijfer, Stefan [2 ]
Debets, Reno [1 ]
Lamers, Cor H. J. [1 ]
机构
[1] Erasmus MC Canc Inst, Lab Tumor Immunol, Rotterdam, Netherlands
[2] Erasmus MC Canc Inst, Dept Med Oncol, Rotterdam, Netherlands
关键词
Renal cell cancer; Chimeric antigen receptor; T-cell; Immune monitoring; Cytokines; IFN-gamma; CLINICAL-EVALUATION; IMMUNOGENE THERAPY; ANTITUMOR-ACTIVITY; ADVERSE EVENT; ANTIGEN; CARCINOMA; GENE; LYMPHOCYTES; PERSISTENCE; TRANSGENE;
D O I
10.1016/j.clim.2016.06.014
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Autologous T-cells genetically modified to express a chimeric antigen receptor (CAR) against carboxy-anhydrase-IX (CAIX) were administered to twelve patients with CAIX-positive metastatic renal cell carcinoma. Here, we questioned whether plasma cytokine levels following treatment or in vitro cytokine production from the T-cell infusion products could serve as predictors for peripheral T-cell persistence or in vivo T-cell activity. We demonstrated that CAR surface as well as gene expression are down-regulated following T-cell infusion, and that peripheral numbers of CAR T-cells are best captured by flow cytometry and not by qPCR. Numbers of CAR T-cells in blood correlated with plasma levels of IFN-gamma and IL-6, but not with any of the other cytokines tested. Plasma IFN-gamma or IL-6 levels did not correlate with liver enzyme values. Thus, out of 27 cytokines tested, IFN-gamma and IL-6 levels in plasma are potential surrogate markers for CAR T-cell persistence in solid tumors. (C) 2016 Published by Elsevier Inc.
引用
收藏
页码:107 / 113
页数:7
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