Additional file 3: Figure S3. of Incorporation of a hinge domain improves the expansion of chimeric antigen receptor T cells

Qin, Le; Lai, Yunxin; Zhao, Ruocong; Wei, Xinru; Weng, Jianyu; Lai, Peilong; Li, Baiheng; Lin, Simiao; Wang, Suna; Wu, Qiting; Liang, Qiubin; Li, Yangqiu; Zhang, Xuchao; Wu, Yilong; Liu, Pentao; Yao, Yao; Pei, Duanqing; Du, Xin; Li, Peng

Links

[dx.doi.org] | PDF

Tools

Export citation

Search in Google Scholar

Additional file 3: Figure S3. of Incorporation of a hinge domain improves the expansion of chimeric antigen receptor T cells

Published in 2017 by Le Qin, Yunxin Lai, Ruocong Zhao, Xinru Wei, Jianyu Weng, Peilong Lai, Baiheng Li, Simiao Lin, Suna Wang, Qiting Wu, Qiubin Liang, Yangqiu Li, Xuchao Zhang, Yilong Wu, Pentao Liu and other authors.

This paper is available in a repository.

Full text: Download

Preprint: policy unknown

Upload

Postprint: policy unknown

Upload

Published version: policy unknown

Upload

Abstract

Percentages of CD4+ and CD8+ CAR T cells without a hinge domain both tended to be stable throughout the in vitro culture period. Flow cytometric analysis of the percentage of CD4+ and CD8+ (A) 19.28z T, (B) Meso.28z T, (C) PSCA.28z T, (D) HER2.28z T, and (E) GFP control T cells during the in vitro culture period. The data are representative of independent experiments verified with cells from over three individual healthy human donors. (JPG 924Â kb)