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Chimeric Antigen Receptor-Modified T Cell Therapy in Multiple Myeloma: Beyond B Cell Maturation Antigen.
Timmers, Marijke; Roex, Gils; Wang, Yuedi; Campillo-Davo, Diana; Van Tendeloo, Viggo F I; Chu, Yiwei; Berneman, Zwi N; Luo, Feifei; Van Acker, Heleen H; Anguille, Sébastien.
Affiliation
  • Timmers M; Division of Hematology, Center for Cell Therapy and Regenerative Medicine, Antwerp University Hospital, Antwerp, Belgium.
  • Roex G; Laboratory of Experimental Hematology, Faculty of Medicine & Health Sciences, Vaccine and Infectious Disease Institute, University of Antwerp, Antwerp, Belgium.
  • Wang Y; Biotherapy Research Center, Fudan University, Shanghai, China.
  • Campillo-Davo D; Laboratory of Experimental Hematology, Faculty of Medicine & Health Sciences, Vaccine and Infectious Disease Institute, University of Antwerp, Antwerp, Belgium.
  • Van Tendeloo VFI; Laboratory of Experimental Hematology, Faculty of Medicine & Health Sciences, Vaccine and Infectious Disease Institute, University of Antwerp, Antwerp, Belgium.
  • Chu Y; Biotherapy Research Center, Fudan University, Shanghai, China.
  • Berneman ZN; Division of Hematology, Center for Cell Therapy and Regenerative Medicine, Antwerp University Hospital, Antwerp, Belgium.
  • Luo F; Laboratory of Experimental Hematology, Faculty of Medicine & Health Sciences, Vaccine and Infectious Disease Institute, University of Antwerp, Antwerp, Belgium.
  • Van Acker HH; Biotherapy Research Center, Fudan University, Shanghai, China.
  • Anguille S; Department of Digestive Diseases, Huashan Hospital of Fudan University, Shanghai, China.
Front Immunol ; 10: 1613, 2019.
Article in En | MEDLINE | ID: mdl-31379824
Chimeric antigen receptor (CAR)-modified T cell therapy is a rapidly emerging immunotherapeutic approach that is revolutionizing cancer treatment. The impressive clinical results obtained with CAR-T cell therapy in patients with acute lymphoblastic leukemia and lymphoma have fueled the development of CAR-T cells targeting other malignancies, including multiple myeloma (MM). The field of CAR-T cell therapy for MM is still in its infancy, but remains promising. To date, most studies have been performed with B cell maturation antigen (BCMA)-targeted CARs, for which high response rates have been obtained in early-phase clinical trials. However, responses are usually temporary, and relapses have frequently been observed. One of the major reasons for relapse is the loss or downregulation of BCMA expression following CAR-T therapy. This has fostered a search for alternative target antigens that are expressed on the MM cell surface. In this review, we provide an overview of myeloma target antigens other than BCMA that are currently being evaluated in pre-clinical and clinical studies.
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Full text: 1 Database: MEDLINE Main subject: T-Lymphocytes / B-Cell Maturation Antigen / Receptors, Chimeric Antigen / Multiple Myeloma Limits: Animals / Humans Language: En Year: 2019 Type: Article

Full text: 1 Database: MEDLINE Main subject: T-Lymphocytes / B-Cell Maturation Antigen / Receptors, Chimeric Antigen / Multiple Myeloma Limits: Animals / Humans Language: En Year: 2019 Type: Article