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Novel CS1 CAR-T Cells and Bispecific CS1-BCMA CAR-T Cells Effectively Target Multiple Myeloma.
Golubovskaya, Vita; Zhou, Hua; Li, Feng; Berahovich, Robert; Sun, Jinying; Valentine, Michael; Xu, Shirley; Harto, Hizkia; Sienkiewicz, John; Huang, Yanwei; Wu, Lijun.
Afiliação
  • Golubovskaya V; Promab Biotechnologies, 2600 Hilltop Drive, Richmond, CA 94806, USA.
  • Zhou H; Promab Biotechnologies, 2600 Hilltop Drive, Richmond, CA 94806, USA.
  • Li F; Promab Biotechnologies, 2600 Hilltop Drive, Richmond, CA 94806, USA.
  • Berahovich R; Biology and Environmental Science College, Hunan University of Arts and Science, Changde 415000, China.
  • Sun J; Promab Biotechnologies, 2600 Hilltop Drive, Richmond, CA 94806, USA.
  • Valentine M; Promab Biotechnologies, 2600 Hilltop Drive, Richmond, CA 94806, USA.
  • Xu S; Promab Biotechnologies, 2600 Hilltop Drive, Richmond, CA 94806, USA.
  • Harto H; Promab Biotechnologies, 2600 Hilltop Drive, Richmond, CA 94806, USA.
  • Sienkiewicz J; Promab Biotechnologies, 2600 Hilltop Drive, Richmond, CA 94806, USA.
  • Huang Y; Promab Biotechnologies, 2600 Hilltop Drive, Richmond, CA 94806, USA.
  • Wu L; Promab Biotechnologies, 2600 Hilltop Drive, Richmond, CA 94806, USA.
Biomedicines ; 9(10)2021 Oct 09.
Article em En | MEDLINE | ID: mdl-34680541
ABSTRACT
Multiple myeloma (MM) is a hematological cancer caused by abnormal proliferation of plasma cells in the bone marrow, and novel types of treatment are needed for this deadly disease. In this study, we aimed to develop novel CS1 CAR-T cells and bispecific CS1-BCMA CAR-T cells to specifically target multiple myeloma. We generated a new CS1 (CD319, SLAM-7) antibody, clone (7A8D5), which specifically recognized the CS1 antigen, and we applied it for the generation of CS1-CAR. CS1-CAR-T cells caused specific killing of CHO-CS1 target cells with secretion of IFN-gamma and targeted multiple myeloma cells. In addition, bispecific CS1-BCMA-41BB-CD3 CAR-T cells effectively killed CHO-CS1 and CHO-BCMA target cells, killed CS1/BCMA-positive multiple myeloma cells, and secreted IFN-gamma. Moreover, CS1-CAR-T cells and bispecific CS1-BCMA CAR-T cells effectively blocked MM1S multiple myeloma tumor growth in vivo. These data for the first time demonstrate that novel CS1 and bispecific CS1-BCMA-CAR-T cells are effective in targeting MM cells and provide a basis for future clinical trials.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Biomedicines Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Biomedicines Ano de publicação: 2021 Tipo de documento: Article