Broadening the horizon: potential applications of CAR-T cells beyond current indications.

Front Immunol

Department of Oncology, Hematology and Bone Marrow Transplantation with Division of Pneumology, University Medical Center Eppendorf, Hamburg, Germany.

Published: December 2023

AI Article Synopsis

  • Engineering immune cells, particularly CAR-T-cell therapies, has advanced significantly in treating hematological malignancies like acute lymphoblastic leukemia (B-ALL) and multiple myeloma, improving outcomes for patients with previously poor prognoses.
  • This review covers current research and innovations in CAR-T-cell therapy for various blood cancers, highlighting strategies applied across different diseases and identifying both common and unique treatment challenges.
  • It also discusses the limitations of CAR-T-cell therapy, including issues with the tumor microenvironment and adverse effects, and hints at future advancements such as artificial intelligence in CAR-T-cell engineering.

Article Abstract

Engineering immune cells to treat hematological malignancies has been a major focus of research since the first resounding successes of CAR-T-cell therapies in B-ALL. Several diseases can now be treated in highly therapy-refractory or relapsed conditions. Currently, a number of CD19- or BCMA-specific CAR-T-cell therapies are approved for acute lymphoblastic leukemia (ALL), diffuse large B-cell lymphoma (DLBCL), mantle cell lymphoma (MCL), multiple myeloma (MM), and follicular lymphoma (FL). The implementation of these therapies has significantly improved patient outcome and survival even in cases with previously very poor prognosis. In this comprehensive review, we present the current state of research, recent innovations, and the applications of CAR-T-cell therapy in a selected group of hematologic malignancies. We focus on B- and T-cell malignancies, including the entities of cutaneous and peripheral T-cell lymphoma (T-ALL, PTCL, CTCL), acute myeloid leukemia (AML), chronic myeloid leukemia (CML), chronic lymphocytic leukemia (CLL), classical Hodgkin-Lymphoma (HL), Burkitt-Lymphoma (BL), hairy cell leukemia (HCL), and Waldenström's macroglobulinemia (WM). While these diseases are highly heterogenous, we highlight several similarly used approaches (combination with established therapeutics, target depletion on healthy cells), targets used in multiple diseases (CD30, CD38, TRBC1/2), and unique features that require individualized approaches. Furthermore, we focus on current limitations of CAR-T-cell therapy in individual diseases and entities such as immunocompromising tumor microenvironment (TME), risk of on-target-off-tumor effects, and differences in the occurrence of adverse events. Finally, we present an outlook into novel innovations in CAR-T-cell engineering like the use of artificial intelligence and the future role of CAR-T cells in therapy regimens in everyday clinical practice.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10711079PMC
http://dx.doi.org/10.3389/fimmu.2023.1285406DOI Listing

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