Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
11030695 | Molecular Immunology | 2018 | 9 Pages |
Abstract
Adoptive cell therapy (ACT) using tumor-specific “conventional” MHC-restricted T cells obtained from tumor-infiltrating lymphocytes, or derived ex vivo by either antigen-specific expansion or genetic engineering of polyclonal T cell populations, shows great promise for cancer treatment. However, the wide applicability of this therapy finds limits in the high polymorphism of MHC molecules that restricts the use in the autologous context. CD1 antigen presenting molecules are nonpolymorphic and specialized for lipid antigen presentation to T cells. They are often expressed on malignant cells and, therefore, may represent an attractive target for ACT. We provide a brief overview of the CD1-resticted T cell response in tumor immunity and we discuss the pros and cons of ACT approaches based on unconventional CD1-restricted T cells.
Keywords
MoDCAMLGvHDiNKTα-GalCerHSCTMLPAAPCACTTCrGVLPBMCTAAMonocyte-derived DCLipid antigentumor-associated antigenantigen-presenting cellTILadoptive cell therapyPeripheral blood mononuclear cellDendritic cellNKT cellsinvariant natural killer Ttumor-infiltrating lymphocyteAcute leukemiaacute myeloid leukemiaAcute lymphoblastic leukemiaCARmajor histocompatibility complexMHCALLGraft versus host diseasegraft versus leukemiaHematopoietic stem cell transplantationchimeric antigen receptorT cell receptor
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Authors
Michela Consonni, Paolo Dellabona, Giulia Casorati,