MR1-restricted T cells: the new dawn of cancer immunotherapy.

Abstract

Cancer immunotherapy has recently undergone rapid development into a validated therapy for clinical use. The adoptive transfer of engineered autologous T cells, such as chimeric antigen receptor (CAR) T cells, has been remarkably successful in patients with leukemia and lymphoma with cluster of differentiation (CD)19 expression. Because of the higher number of antigen choices and reduced incidence of cytokine release syndrome (CRS) than CAR-T cells, T cell receptor (TCR)-T cells are also considered a promising immunotherapy. More therapeutic targets for other cancers need to be explored due to the human leukocyte antigen (HLA)-restricted recognition of TCR-T. Major histocompatibility complex (MHC), class I-related (MR1)-restricted T cells can recognize metabolites presented by MR1 in the context of host cells infected with pathogens. MR1 is expressed by all types of human cells. Recent studies have shown that one clone of a MR1-restricted T (MR1-T) cell can recognize many types of cancer cells without HLA-restriction. These studies provide additional information on MR1-T cells for cancer immunotherapy. This review describes the complexity of MR1-T cell TCR in diseases and the future of cancer immunotherapy.

• Authors: Zhiding Wang, Mengzhen Wang, Jinghong Chen, Linlin Zhang, Li Zhang, Li Yu
• Journal: Bioscience reports (Biosci Rep) Vol. 40 Issue 11 (11 27 2020) ISSN: 1573-4935 [Electronic] England
• PMID: 33185693 (Publication Type: Journal Article, Review)
• Copyright: © 2020 The Author(s).

Chemical References

• Histocompatibility Antigens Class I
• MR1 protein, human
• Minor Histocompatibility Antigens

Topics

• Animals
• Histocompatibility Antigens Class I (genetics, immunology, metabolism)
• Humans
• Immunotherapy, Adoptive
• Lymphocytes, Tumor-Infiltrating (immunology, metabolism)
• Minor Histocompatibility Antigens (genetics, immunology, metabolism)
• Mucosal-Associated Invariant T Cells (immunology, metabolism)
• Neoplasms (genetics, immunology, metabolism, therapy)
• Phenotype
• Prognosis
• T-Lymphocytes (immunology, metabolism, transplantation)