Identification of α‐fetoprotein‐specific T‐cell receptors for hepatocellular carcinoma immunotherapy. Issue 2 (12th June 2018)
- Record Type:
- Journal Article
- Title:
- Identification of α‐fetoprotein‐specific T‐cell receptors for hepatocellular carcinoma immunotherapy. Issue 2 (12th June 2018)
- Main Title:
- Identification of α‐fetoprotein‐specific T‐cell receptors for hepatocellular carcinoma immunotherapy
- Authors:
- Zhu, Wei
Peng, Yibing
Wang, Lan
Hong, Yuan
Jiang, Xiaotao
Li, Qi
Liu, Heping
Huang, Lei
Wu, Juan
Celis, Esteban
Merchen, Todd
Kruse, Edward
He, Yukai - Abstract:
- Abstract : Hepatocellular carcinoma (HCC) is the major form of liver cancer for which there is no effective therapy. Genetic modification with T‐cell receptors (TCRs) specific for HCC‐associated antigens, such as α‐fetoprotein (AFP), can potentially redirect human T cells to specifically recognize and kill HCC tumor cells to achieve antitumor effects. In this study, using lentivector and peptide immunization, we identified a population of cluster of differentiation 8 (CD8) T cells in human leukocyte antigen (HLA)‐A2 transgenic AAD mice that recognized AFP158 epitope on human HCC cells. Adoptive transfer of the AFP158 ‐specific mouse CD8 T cells eradicated HepG2 tumor xenografts as large as 2 cm in diameter in immunocompromised nonobese diabetic severe combined immunodeficient gamma knockout (NSG) mice. We then established T‐cell hybridoma clones from the AFP158 ‐specific mouse CD8 T cells and identified three sets of paired TCR genes out of five hybridomas. Expression of the murine TCR genes redirected primary human T cells to bind HLA‐A2/AFP158 tetramer. TCR gene‐engineered human T (TCR‐T) cells also specifically recognized HLA‐A2 + AFP + HepG2 HCC tumor cells and produced effector cytokines. Importantly, the TCR‐T cells could specifically kill HLA‐A2 + AFP + HepG2 tumor cells without significant toxicity to normal primary hepatocytes in vitro . Adoptive transfer of the AFP‐specific TCR‐T cells could eradicate HepG2 tumors in NSG mice. Conclusion: We have identifiedAbstract : Hepatocellular carcinoma (HCC) is the major form of liver cancer for which there is no effective therapy. Genetic modification with T‐cell receptors (TCRs) specific for HCC‐associated antigens, such as α‐fetoprotein (AFP), can potentially redirect human T cells to specifically recognize and kill HCC tumor cells to achieve antitumor effects. In this study, using lentivector and peptide immunization, we identified a population of cluster of differentiation 8 (CD8) T cells in human leukocyte antigen (HLA)‐A2 transgenic AAD mice that recognized AFP158 epitope on human HCC cells. Adoptive transfer of the AFP158 ‐specific mouse CD8 T cells eradicated HepG2 tumor xenografts as large as 2 cm in diameter in immunocompromised nonobese diabetic severe combined immunodeficient gamma knockout (NSG) mice. We then established T‐cell hybridoma clones from the AFP158 ‐specific mouse CD8 T cells and identified three sets of paired TCR genes out of five hybridomas. Expression of the murine TCR genes redirected primary human T cells to bind HLA‐A2/AFP158 tetramer. TCR gene‐engineered human T (TCR‐T) cells also specifically recognized HLA‐A2 + AFP + HepG2 HCC tumor cells and produced effector cytokines. Importantly, the TCR‐T cells could specifically kill HLA‐A2 + AFP + HepG2 tumor cells without significant toxicity to normal primary hepatocytes in vitro . Adoptive transfer of the AFP‐specific TCR‐T cells could eradicate HepG2 tumors in NSG mice. Conclusion: We have identified AFP‐specific murine TCR genes that can redirect human T cells to specifically recognize and kill HCC tumor cells, and those AFP158 ‐specific TCRs have a great potential to engineer a patient's autologous T cells to treat HCC tumors. (Hepatology 2018). … (more)
- Is Part Of:
- Hepatology. Volume 68:Issue 2(2018)
- Journal:
- Hepatology
- Issue:
- Volume 68:Issue 2(2018)
- Issue Display:
- Volume 68, Issue 2 (2018)
- Year:
- 2018
- Volume:
- 68
- Issue:
- 2
- Issue Sort Value:
- 2018-0068-0002-0000
- Page Start:
- 574
- Page End:
- 589
- Publication Date:
- 2018-06-12
- Subjects:
- Heart -- Diseases -- Nursing -- Periodicals
Lungs -- Diseases -- Nursing -- Periodicals
Intensive care nursing -- Periodicals
Foie -- Maladies -- Périodiques
616.362 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1527-3350 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/hep.29844 ↗
- Languages:
- English
- ISSNs:
- 0270-9139
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4295.836000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 11485.xml