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How do CARs work?: Early insights from recent clinical studies targeting CD19

Second-generation chimeric antigen receptors (CARs) are powerful tools to redirect antigen-specific T cells independently of HLA-restriction. Recent clinical studies evaluating CD19-targeted T cells in patients with B-cell malignancies demonstrate the potency of CAR-engineered T cells. With results...

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Detalles Bibliográficos
Autores principales: Davila, Marco L., Brentjens, Renier, Wang, Xiuyan, Rivière, Isabelle, Sadelain, Michel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3525612/
https://www.ncbi.nlm.nih.gov/pubmed/23264903
http://dx.doi.org/10.4161/onci.22524
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author Davila, Marco L.
Brentjens, Renier
Wang, Xiuyan
Rivière, Isabelle
Sadelain, Michel
author_facet Davila, Marco L.
Brentjens, Renier
Wang, Xiuyan
Rivière, Isabelle
Sadelain, Michel
author_sort Davila, Marco L.
collection PubMed
description Second-generation chimeric antigen receptors (CARs) are powerful tools to redirect antigen-specific T cells independently of HLA-restriction. Recent clinical studies evaluating CD19-targeted T cells in patients with B-cell malignancies demonstrate the potency of CAR-engineered T cells. With results from 28 subjects enrolled by five centers conducting studies in patients with chronic lymphocytic leukemia (CLL) or lymphoma, some insights into the parameters that determine T-cell function and clinical outcome of CAR-based approaches are emerging. These parameters involve CAR design, T-cell production methods, conditioning chemotherapy as well as patient selection. Here, we discuss the potential relevance of these findings and in particular the interplay between the adoptive transfer of T cells and pre-transfer patient conditioning.
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spelling pubmed-35256122012-12-21 How do CARs work?: Early insights from recent clinical studies targeting CD19 Davila, Marco L. Brentjens, Renier Wang, Xiuyan Rivière, Isabelle Sadelain, Michel Oncoimmunology Review Second-generation chimeric antigen receptors (CARs) are powerful tools to redirect antigen-specific T cells independently of HLA-restriction. Recent clinical studies evaluating CD19-targeted T cells in patients with B-cell malignancies demonstrate the potency of CAR-engineered T cells. With results from 28 subjects enrolled by five centers conducting studies in patients with chronic lymphocytic leukemia (CLL) or lymphoma, some insights into the parameters that determine T-cell function and clinical outcome of CAR-based approaches are emerging. These parameters involve CAR design, T-cell production methods, conditioning chemotherapy as well as patient selection. Here, we discuss the potential relevance of these findings and in particular the interplay between the adoptive transfer of T cells and pre-transfer patient conditioning. Landes Bioscience 2012-12-01 /pmc/articles/PMC3525612/ /pubmed/23264903 http://dx.doi.org/10.4161/onci.22524 Text en Copyright © 2012 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Review
Davila, Marco L.
Brentjens, Renier
Wang, Xiuyan
Rivière, Isabelle
Sadelain, Michel
How do CARs work?: Early insights from recent clinical studies targeting CD19
title How do CARs work?: Early insights from recent clinical studies targeting CD19
title_full How do CARs work?: Early insights from recent clinical studies targeting CD19
title_fullStr How do CARs work?: Early insights from recent clinical studies targeting CD19
title_full_unstemmed How do CARs work?: Early insights from recent clinical studies targeting CD19
title_short How do CARs work?: Early insights from recent clinical studies targeting CD19
title_sort how do cars work?: early insights from recent clinical studies targeting cd19
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3525612/
https://www.ncbi.nlm.nih.gov/pubmed/23264903
http://dx.doi.org/10.4161/onci.22524
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