HBV-HCC treatment with mRNA electroporated HBV-TCR T cells

被引:13
作者
Tan, Anthony T. [1 ]
Bertoletti, Antonio [1 ,2 ]
机构
[1] Duke NUS Med Sch, Emerging Infect Dis, Singapore, Singapore
[2] ASTAR, Singapore Immunol Network, Singapore, Singapore
来源
IMMUNOTHERAPY ADVANCES | 2022年 / 2卷 / 01期
基金
英国医学研究理事会;
关键词
T-cell immunotherapy; hepatocellular carcinoma; hepatitis B; tumour microenvironment; HEPATOCELLULAR-CARCINOMA; IMMUNOTHERAPY; EXPRESSION; SORAFENIB; RECEPTOR; CANCER; LANDSCAPE;
D O I
10.1093/immadv/ltab026
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Hepatocellular carcinoma is a significant global health challenge with steadily increasing incidence in the East Asia region. While both Hepatitis C and B virus infections account for the majority of HCC cases, the advent of potent antivirals against HCV infection has biased the aetiology towards chronic HBV infection that at the moment remains without an effective cure. For this reason, HBV-HCC remains a persistent global problem. Treatment options for intermediate to advanced stages of HBV-HCC remain limited, hence novel therapeutic strategies are required to fulfil this medical need. Following the considerable success of adoptive T-cell immunotherapy against B-cell malignancies, it is conceivable to envision whether the same could be achieved against HBV-HCC. In this review, we describe the development of T-cell therapy strategies for HBV-HCC and discuss the safety and the efficacy of the strategies in terms of the direct killing of tumour cells and the other alterations possibly induced by the action of the T cells. [GRAPHICS] .
引用
收藏
页数:7
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