Your browser doesn't support javascript.
loading
CAR T cells for treating autoimmune diseases.
Blache, Ulrich; Tretbar, Sandy; Koehl, Ulrike; Mougiakakos, Dimitrios; Fricke, Stephan.
Afiliação
  • Blache U; Fraunhofer Institute for Cell Therapy and Immunology IZI, Leipzig, Germany ulrich.blache@izi.fraunhofer.de.
  • Tretbar S; Fraunhofer Cluster of Excellence for Immune-Mediated Disease, Leipzig, Germany.
  • Koehl U; Fraunhofer Institute for Cell Therapy and Immunology IZI, Leipzig, Germany.
  • Mougiakakos D; Fraunhofer Cluster of Excellence for Immune-Mediated Disease, Leipzig, Germany.
  • Fricke S; Fraunhofer Institute for Cell Therapy and Immunology IZI, Leipzig, Germany.
RMD Open ; 9(4)2023 11 23.
Article em En | MEDLINE | ID: mdl-37996128
ABSTRACT
Autoimmune disorders occur when immune cells go wrong and attack the body's own tissues. Currently, autoimmune disorders are largely treated by broad immunosuppressive agents and blocking antibodies, which can manage the diseases but often are not curative. Thus, there is an urgent need for advanced therapies for patients suffering from severe and refractory autoimmune diseases, and researchers have considered cell therapy as potentially curative approach for several decades. In the wake of its success in cancer therapy, adoptive transfer of engineered T cells modified with chimeric antigen receptors (CAR) for target recognition could now become a therapeutic option for some autoimmune diseases. Here, we review the ongoing developments with CAR T cells in the field of autoimmune disorders. We will cover first clinical results of applying anti-CD19 and anti-B cell maturation antigen CAR T cells for B cell elimination in systemic lupus erythematosus, refractory antisynthetase syndrome and myasthenia gravis, respectively. Furthermore, in preclinical models, researchers have also developed chimeric autoantibody receptor T cells that can eliminate individual B cell clones producing specific autoantibodies, and regulatory CAR T cells that do not eliminate autoreactive immune cells but dampen their wrong activation. Finally, we will address safety and manufacturing aspects for CAR T cells and discuss mRNA technologies and automation concepts for ensuring the future availability of safe and efficient CAR T cell products.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doenças Autoimunes / Receptores de Antígenos Quiméricos Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doenças Autoimunes / Receptores de Antígenos Quiméricos Idioma: En Ano de publicação: 2023 Tipo de documento: Article