TY - JOUR
T1 - Engineering T cells for immunotherapy of primary human hepatocellular carcinoma
AU - Caraballo Galva, Leidy D.
AU - Cai, Lun
AU - Shao, Yanxia
AU - He, Yukai
N1 - Funding Information:
Research in Dr. Yukai He's laboratory on developing TCRTs and CART for HCC immunotherapy has been supported by NIH/NCI grants (R01CA168912 and R01CA235159) and Augusta University intramural grant. We would like to thank Ms. Yibing Peng and all previous members of Dr. Yukai He's laboratory for their contribution on developing the HCC specific TCRT and CART projects.
Funding Information:
Research in Dr. Yukai He's laboratory on developing TCRTs and CART for HCC immunotherapy has been supported by NIH/NCI grants ( R01CA168912 and R01CA235159 ) and Augusta University intramural grant. We would like to thank Ms. Yibing Peng and all previous members of Dr. Yukai He's laboratory for their contribution on developing the HCC specific TCRT and CART projects.
Publisher Copyright:
© 2020 Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, and Genetics Society of China
PY - 2020/1/20
Y1 - 2020/1/20
N2 - Liver cancers, majority of which are primary hepatocellular carcinoma (HCC), continue to be on the rise in the world. Furthermore, due to the lack of effective treatments, liver cancer ranks the 4th most common cause of male cancer deaths. Novel therapies are urgently needed. Over the last few years, immunotherapies, especially the checkpoint blockades and adoptive cell therapies of engineered T cells, have demonstrated a great potential for treating malignant tumors including HCC. In this review, we summarize the current ongoing research of antigen-specific immunotherapies including cancer vaccines and adoptive cell therapies for HCC. We briefly discuss the HCC cancer vaccine and then focus on the antigen-specific T cells genetically engineered with the T cell receptor genes (TCRTs) and the chimeric antigen receptor genes (CARTs). We first review the current options of TCRTs and CARTs immunotherapies for HCC, and then analyze the factors and parameters that may help to improve the design of TCRTs and CARTs to enhance their antitumor efficacy and safety. Our goals are to render readers a panoramic view of the current stand of HCC immunotherapies and provide some strategies to design better TCRTs and CARTs to achieve more effective and durable antitumor effects.
AB - Liver cancers, majority of which are primary hepatocellular carcinoma (HCC), continue to be on the rise in the world. Furthermore, due to the lack of effective treatments, liver cancer ranks the 4th most common cause of male cancer deaths. Novel therapies are urgently needed. Over the last few years, immunotherapies, especially the checkpoint blockades and adoptive cell therapies of engineered T cells, have demonstrated a great potential for treating malignant tumors including HCC. In this review, we summarize the current ongoing research of antigen-specific immunotherapies including cancer vaccines and adoptive cell therapies for HCC. We briefly discuss the HCC cancer vaccine and then focus on the antigen-specific T cells genetically engineered with the T cell receptor genes (TCRTs) and the chimeric antigen receptor genes (CARTs). We first review the current options of TCRTs and CARTs immunotherapies for HCC, and then analyze the factors and parameters that may help to improve the design of TCRTs and CARTs to enhance their antitumor efficacy and safety. Our goals are to render readers a panoramic view of the current stand of HCC immunotherapies and provide some strategies to design better TCRTs and CARTs to achieve more effective and durable antitumor effects.
KW - Chimeric antigen receptor
KW - Gene transfer
KW - Hepatocellular carcinoma
KW - Immunotherapy
KW - T cell engineering
KW - T cell receptor
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U2 - 10.1016/j.jgg.2020.01.002
DO - 10.1016/j.jgg.2020.01.002
M3 - Review article
C2 - 32089500
AN - SCOPUS:85079845030
SN - 1673-8527
VL - 47
SP - 1
EP - 15
JO - Journal of Genetics and Genomics
JF - Journal of Genetics and Genomics
IS - 1
ER -