Tissue-Resident Lymphocytes: Implications in Immunotherapy for Hepatocellular Carcinoma.
Ji-Won HanSeung Kew YoonPublished in: International journal of molecular sciences (2020)
Hepatocellular carcinoma (HCC) is a hard-to-treat cancer. The recent introduction of immune checkpoint inhibitors (ICIs) provided viable options to treat HCC, but the response rate is currently not sufficient. Thus, a better understanding of ICI-responding cells within tumors is needed to improve outcomes of ICI treatment in HCC. Recently, tissue-resident memory T (TRM) cells were defined as a subset of the memory T cell population; this cell population is actively under investigation to elucidate its role in anti-tumor immunity. In addition, the role of other tissue-resident populations such as tissue resident regulatory T (Treg) cells, mucosal associated invariant T (MAIT) cells, γδ T cells, and invariant natural killer T (iNKT) cells in anti-tumor immunity is also actively being investigated. However, there is no study that summarizes recent studies and discusses future perspectives in terms of tissue resident lymphocytes in HCC. In this review, we summarize key features of tissue-resident lymphocytes and their role in the anti-tumor immunity. Additionally, we review recent studies regarding the characteristics of tissue-resident lymphocytes in HCC and their role in ICI treatment and other immunotherapeutic strategies.
Keyphrases
- induced apoptosis
- patient safety
- cell cycle arrest
- quality improvement
- endoplasmic reticulum stress
- peripheral blood
- signaling pathway
- oxidative stress
- type diabetes
- transcription factor
- single cell
- high resolution
- adipose tissue
- working memory
- emergency medicine
- skeletal muscle
- cell therapy
- combination therapy
- single molecule
- smoking cessation
- lymph node metastasis
- squamous cell
- high speed