Next-Generation CAR T-cell Therapies

Author:

Young Regina M.12ORCID,Engel Nils W.1ORCID,Uslu Ugur1,Wellhausen Nils1,June Carl H.12ORCID

Affiliation:

1. 1Center for Cellular Immunotherapies, Department of Pathology and Laboratory Medicine, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania.

2. 2Parker Institute for Cancer Immunotherapy at University of Pennsylvania, Philadelphia, Pennsylvania.

Abstract

Summary:CD19- and B-cell maturation antigen (BCMA)–directed chimeric antigen receptor (CAR) T cells have enabled unprecedented responses in a subset of refractory patients with B-cell and plasma cell malignancies, leading to their approval by the FDA for the treatment of leukemia, lymphoma, and myeloma. These “living drugs” can become part of a synthetic immune system, persisting at least a decade in some patients. However, despite this tremendous impact, significant unmet treatment needs remain for patients with hematologic malignancies and solid cancers. In this perspective, we highlight recent innovations that advance the field toward production of a more potent and universal cellular immunotherapy of the future. Next-generation CAR T cells will incorporate advances in gene engineering and synthetic biology to enhance functionality and persistence, and reduce treatment-associated toxicities. The combination of autologous CAR T cells with various allogeneic cell treatment strategies designed to target the immunosuppressive tumor microenvironment will broaden the impact of future CAR T-cell therapies.

Funder

NIH

Publisher

American Association for Cancer Research (AACR)

Subject

Oncology

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